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عضویت

جستجوی مقالات مرتبط با کلیدواژه "tissue scaffolds" در نشریات گروه "پزشکی"

  • Omid Tavallaei, Mahtab Doostan, Kamyar Khoshnevisan, Ali Tahmasebi, Hassan Maleki *
    Objective (s)

    Natural component-included scaffolds can provide numerous benefits for skin healing and tissue regeneration. Nanofibers (NFs) with intricately intertwined three-dimensional structures afford an exclusive matrix for delivering therapeutics. This research assessed nanofibrous scaffolds loaded with Achillea wilhelmsii extract (5-15 wt%) for skin tissue engineering. 

    Materials and Methods

    A. wilhelmsii-loaded scaffolds, composed of poly(vinyl alcohol) (PVA) and chitosan (CS), were fabricated by the electrospinning process. Subsequently, the physicochemical properties of the scaffolds were evaluated through relevant analyses. The antioxidant activity and degradation rate of the scaffolds were also determined. Cell viability and scratch assays on dermal fibroblasts were conducted to assess proliferation and migration activities.  

    Results

    Electron micrographs revealed interconnected fibers with a nano-scale diameter (> 400 nm) and uniform morphology. Additionally, the intact presence of A. wilhelmsii extract in the polymeric matrix was confirmed without any undesirable interactions. The proposed scaffolds verified favorable mechanical properties, a hydrophilic nature, high volume porosity (>90%), and water absorption capability (<500%). Besides, the findings demonstrated the remarkable radical scavenging ability of A. wilhelmsii extract in the nanofibrous scaffolds, along with controlled degradation kinetics over 72 h. The viability assay proved that the A. wilhelmsii-loaded scaffolds not only exhibited no cytotoxicity but also improved cell proliferation. The scaffolds also significantly accelerated fibroblast migration and complete closure of scratched areas. 

    Conclusion

    At last, the obtained results revealed that A. wilhelmsii-loaded PVA/CS NFs can be applied as a potential scaffold for skin regeneration and wound healing promotion.

    Keywords: Antioxidants, Electrospinning, Nanofibers, Tissue Scaffolds, Wound Healing
  • Hojat Rezazadeh, Nazafarin Samiraninezhad *, Mostafa Rezaee

    Defects and dysfunctions of temporomandibular joint (TMJ) disc are responsible for the majority of TMJ diseases. Current treatments in this matter are usually short-term and only palliative, thus an alternative treatment that offers long-lasting repair is in great demand. In recent years great attempts have been made to prepare an ideal scaffold which best resembles the native TMJ disc in characteristics such as mechanical, physical and biological properties. This narrative review focuses on developments of the recent ten years in fabrication of scaffolds using decellularized tissues, natural and synthetic biomaterials for regeneration of TMJ disc and compared their properties. PubMed and Google Scholar databases were searched using the following keywords (“TMJ” OR “temporomandibular joint” OR “TMD” OR “temporomandibular disease”) AND (“scaffold” OR “hydrogels”). Randomized controlled trials, randomized clinical trials, case-controls, case reports, and animal studies were included. Comments, systematic reviews, meta-analyses, and non-English papers were excluded. The study concluded that hybrid scaffolds have exhibited favorable cell attachment and proliferation. Synthetic scaffolds have shown promise in providing better control over structural properties; however, additional processes are often required to provide biomimetic cell signaling. While there is still much to learn about the ideal scaffold for TMJ disc regeneration, both natural and synthetic scaffolds have shown promise in achieving the functional, structural, biological, and mechanical properties of a native TMJ disc.

    Keywords: Temporomandibular Joint Disc, Regeneration, Tissue Scaffolds, Hydrogels, Decellularized Extracellular Matrix
  • Seyed Hossein Asadi‐Yousefabad, Sajad Daneshi, Majid Pourentezari, Nader Tanideh, Mohammad Zamani Rarani, Hengameh Dortaj, Mojtaba Salari, Zeinolabedin Sharifian Dastjerdi *
    Background
    Sodium dodecyl sulfate (SDS) detergent is widely used in tissue decellularization to produce scaffolds for tissue engineering. Despite its strong decellularization, this substance has relatively high toxicity and causes changes in tissue composition. Sodium lauryl ether sulfate (SLES) is a new poly anionic detergent that is less toxic than SDS but weaker than it. The present study aimed to decellularize the intestinal tissue using SDS and SLES solutions, forming a cell scaffold, and examining scaffolds obtained from this tissue.
    Methods
    Eighteen male Sprague-Dawley rats were divided into three groups. The intestines of all rats were removed after anesthesia. In the first group (controls), rats’ intestines were placed in a 10% formalin solution. In the second group, intestines were decellularized using an SLES solution. In the third group animals’ intestines were decellularized using an SDS solution. To evaluate decellularization, samples were stained with hematoxylin-eosin staining and Alcian blue staining for glycosaminoglycans (GAGs), and Masson’s trichrome for collagen fibers. A confocal Raman microscope was used to compare collagen, lipid, GAG, and genetic content.
    Results
    Hematoxylin-eosin staining showed that the nucleus and DNA were removed in the decellularized scaffolds by SDS or SLES. The SLES group, compared to the SDS group, showed fewer changes in the epithelial tissue, and muscle layers in both scaffolds were well preserved. The results of confocal Raman microscopy showed that tryptophan, lipid, glycogen, and protein were broken down by both detergents; however, the residual amount of glycogen was the same in both substances, but disulfide bonds of proteins, hydroxyproline, and lipids in the decellularized intestine with SLES were mostly preserved.
    Conclusion
    Both substances were suitable for intestinal decellularization and removed the overall structure of intestinal tissue, but SLES retained collagen and GAG content better than SDS.
    Keywords: Tissue engineering, Intestinal failure, Tissue scaffolds, Decellularized extracellular matrix, Sodium dodecyl sulfate
  • Timothy Cobb, Richard Dimock, Sahib Memon, Paolo Consigliere, Sam Ajami, Mohamed Imam, A. Ali Narvani *
    Background

    Repair of massive rotator cuff tears remains a challenging process with mixed success. There is agrowing interest in the use of patches to augment the repair construct and the potential to enhance the strength,healing, and associated clinical outcomes. Such patches may be synthetic, xenograft, or autograft/allograft, and avariety of techniques have been tried to biologically enhance their integration and performance. The materials used arerapidly advancing, as is our understanding of their effects on rotator cuff tissue. This article aims to evaluate what wecurrently know about patch augmentation through a comprehensive review of the available literature.

    Methods

    We explore the results of existing clinical trials for each graft type, new manufacturing methods, noveltechniques for biological enhancement, and the histological and biomechanical impact of patch augmentation.

    Results

    There are promising results in short-term studies, which suggest that patch augmentation has greatpotential to improve the success rate. In particular, this appears to be true for human dermal allograft, while porcinedermal grafts and some synthetic grafts have also had promising results.

    Conclusion

    However, there remains a need for high-quality, prospective clinical trials directly comparing each type ofgraft and the effect that they have on the clinical and radiological outcomes of rotator cuff repair. 

    Keywords: biological enhancement, Extracellular matrix, patch augmentation, Rotator Cuff, Rotator cuff repair, Rotator cuff tear, tissue scaffolds
  • Mobin Haghdel, MohammadHadi Imanieh, Hamidreza Hosseinpour, Younes Ghasemi, AliAkbar Alizadeh *

    The esophagus is the gastrointestinal tract’s primary organ that transfers bolus into the stomach with peristaltic motion. Therefore, its lesions cause a significant disturbance in the nutrition and digestive system. Esophageal disease treatment sometimes requires surgical procedures that involve removal and circumferential full-thickness replacement. Unlike other organs, the esophagus has a limited regeneration ability and cannot be transplanted from donors. There are various methods of restoring the esophageal continuity; however, they are associated with certain flaws that lead to a non-functional recovery. As an exponentially growing science, tissue engineering has become a leading technique for the development of tissue replacement to repair damaged esophageal segments. Scaffold plays a significant role in the process of tissue engineering, as it acts as a template for the regeneration of growing tissue. A variety of scaffolds have been studied to replace the esophagus. Due to the many tissue quality challenges, the results are still inadequate and need to be improved. The success of esophageal tissue regeneration will finally depend on the scaffold’s capability to mimic natural tissue properties and provide a qualified environment for regeneration. Thereby, scaffold fabrication techniques are fundamental. This article reviews the recent developments in esophageal tissue engineering for the treatment of circumferential lesions based on scaffold biomaterial engineering approaches.

    Keywords: Tissue engineering, Esophagus, stem cells, Biocompatible Materials, Tissue scaffolds, Regeneration
  • Parisa Amdjadi *, Kimia Khoshroo, Massoud Seifi, Mohammadreza Tahriri, Lobat Tayebi

    Objectives

    This paper describes the fabrication of a new porous 3D-printed scaffold composed of polycaprolactone (PCL) and polyether-ether ketone (PEEK) micro-particles for bone tissue engineering (BTE) applications.

    Methods

    In order to improve the compatibility of the reinforcing PEEK powder with polycaprolactone, the PEEK powder was surface-modified by an amino-silane coupling agent. After modification, Fourier-transform infrared spectrometry (FTIR) and differential scanning calorimetry (DSC) were used to investigate the chemical reaction between PEEK and silane coupling agent. In order to increase the compressive modulus of the 3D printed PCL scaffold, 10% silane-modified PEEK was incorporated into the PCL polymeric matrix. Scanning electron microscopy (SEM) was used for cell morphology and attachment evaluation.

    Results 

    The results indicated that the silane coupling agent was successfully grafted onto the particle surface. The compressive modulus of PCL scaffold increased by incorporating the silane-modified PEEK, despite having higher porosity, compared with the pure PCL scaffolds. Addition of amino-silane had a positive impact on cell response, and that surface modification led to improved particle dispersion.

    Conclusion

    In conclusion, it seems that the incorporation of surface-modified PEEK micro-particles into the PCL porous scaffold could enhance its mechanical properties, and may be applicable for the management of large bone defects.Keywords Polyetheretherketone; Polycaprolactone; Amino-propyl-triethoxysilane; Tissue Scaffolds; Printing, Three-Dimensional

    Keywords: Polyetheretherketone, Polycaprolactone, Amino-propyl-triethoxysilane, Tissue Scaffolds, Printing, Three-Dimensional
  • Omid Moghaddas*, Behdokht Miremadi, Ehsan Seyed Jafari

    Background:

    Periodontal regeneration is an essential goal of periodontal therapy. Acellular dermal matrix (ADM) has been recommended as an alternative to autogenous grafts. However, since it is devoid of cells and vasculature, there are concerns regarding the biological behavior of cells on ADM. This study aimed to assess the effects of two commonly used ADMs on biological behavior, i.e., attachment and proliferation, of human gingival fibroblasts (HGFs).

    Methods:

    This in vitro, experimental study was conducted on explanted and cultured HGFs. ADM types 1 and 2 (n=26; measuring 10×15 mm) were rinsed with saline solution, adapted to the bottom of 52 wells, exposed to HGFs with a cell density of 16,000 cells/mL, and incubated at 37°C for 12, 24, and 84 hours and seven days. Cell attachment was assessed 12 hours after incubation using 4›,6-diamidino-2-phenylindole (DAPI) and methyl-thiazol-diphenyl-tetrazolium (MTT) assay under a fluorescence microscope. Cell viability was assessed at 24 and 84 hours and one week using the MTT assay. Cells were then platinum-coated, and their morphology was evaluated under a scanning electron microscope (SEM). Data were analyzed using ANOVA.

    Results:

     HGFs were evaluated in 60 samples in three groups (n=20). Cell attachment was the same in the three groups, as shown by the MTT assay and DAPI test (P=0.6). Cell viability at one week was 3.73±0.02, 2.88±0.29, and 2.13±0.24 in the control, ADM 1, and ADM 2 groups, respectively. The difference was statistically significant (P=0.01).

    Conclusion:

    Both scaffolds were the same in terms of attachment of HGFs. However, ADM 1 was superior to ADM2 in terms of cell viability and morphology at one week. It was concluded that the quality of acellular dermal scaffolds could significantly influence cellular behaviors and tissue maturation.

    Keywords: Acellular dermis, Cell survival, Fibroblasts, Tissue scaffolds
  • Zeinolabedin Sharifian, Batool Hashemibeni, Majid Pourentezari*, Ali Valiani, Mohammad Mardani, Mohammad Zamani Rarani, Hamidreza Pourentezari
    Background and Aims

    Tissue engineering is a relatively novel field that has been intensely developing during recent years and has shown to be excessively promising when used for cartilage regeneration. Scaffolds represent important components for tissue engineering.

    Materials and Methods

    The Poly Lactic-Co-Glycolic Acid (PLGA) impregnated with fibrin and hyaluronic acid (HA) produce hybrid scaffolds. human adipose-derived stem cells (hADSCs) were seeded in scaffolds and cultured in chondrogenic media. The viability of cells in different groups was assessed by MTT. The expression of chondrogenic related genes [Sox9, type II collagen (Col II), Aggrecan(AGG)] and type X collagen (Col X) was quantified by real-time polymerase chain reaction.

    Results

    The results of the real-time PCR showed SOX9, AGG and Col X gene expression in the control groups being significantly lower than the other groups (p≤0.05). It also demonstrated Col II gene expression in the control group being significantly lower than the PLGA/Fibrin and PLGA/Fibrin/HA groups (p≤0.05). The Col X gene expression of cells in PLGA/HA and PLGA/Fibrin/HA groups significantly decreased in comparison with the PLGA/Fibrin group (p≤0.05).

    Conclusions

    These conclusions indicate that administration of PLGA/ Fibrin and PLGA/HA scaffolds, particularly PLGA/Fibrin/ HA, motivates chondrogenesis in hADSCs. This can be diminished by decreasing hypertrophic markers and increasing characteristic markers of hyaline cartilage.

    Keywords: Copolymer, Hyaluronic acid, Mesenchymal stem cells, Polylactic acid-polyglycolic acid, Tissue scaffolds
  • Behnam Bolhari, Naghmeh Meraji, Abdollah Ghorbanzadeh, Pegah Sarraf, Razieh Moayeri
    Introduction

    Endodontic treatment of necrotic immature teeth is quite challenging. Current concepts for revitalization of these teeth known as regenerative endodontic treatment (RET) is based on key elements necessary for tissue engineering including stem cells, three-dimensional (3D) scaffolds, and growth factors. Utilizing an applicable scaffold for narrow root canal space with adequate properties is essential for successful outcome. Fibrin-based products are materials with various advantages as a scaffold. This review article aims to discuss the properties of different types of fibrin-based products and debates whether they are appropriate scaffolds for RET or not?

    Methods

    An electronic search was performed using databases such as Google Scholar, PubMed, PubMed Central, Science Direct, and Scopus. Keywords such as (“scaffold”) AND (“fibrin gel” OR “fibrin sealant” OR “fibrin glue” OR “fibrin tissue adhesive” OR “fibrin hydrogel” OR “platelet concentrate”) AND (“tooth” OR “teeth”) AND/OR (“regenerative endodontics” OR “dentistry”) were used. Exclusion criteria included studies published in a language other than English and abstracts from congress.

    Results

    Fibrin gel is a protein-based natural polymer hydrogel scaffold which can be easily used in the root canal. Platelet concentrates are autologous fibrin-based products used as scaffolds for RET with various favorable properties especially due to containing various growth factors.

    Conclusion

    It seems that fibrin gel and platelet concentrates have adequate properties for use in RET; however, more evidence is required regarding the clinical outcome of applying these products as scaffolds for RET.

    Keywords: Fibrin, fibrin tissue adhesive, hydrogel, platelet concentrates, regenerative endodontics, tissue engineering, tissue scaffolds
  • آرش عبدالملکی*، محمد باقر غیور، صابر زهری، اسدالله اسدی، مرتضی بهنام رسولی
    زمینه و هدف
    مهندسی بافت یک موضوع چندرشته ای و بین رشته ای است که شامل توسعه ایمپلنت های زیستی برای بازسازی بافت با هدف بهبود یا افزایش عملکرد بافت یا اندام می باشد. هدف از پژوهش حاضر ارزیابی ویژگی های مکانیکی و هیستولوژیکی داربست های سلول زدایی شده عصبی تهیه شده در مقایسه با عصب تازه جهت کاربرد در ترمیم اعصاب محیطی بود.
    روش بررسی
    این مطالعه از نوع تجربی می باشد که در آزمایشگاه تحقیقاتی ترمیم اعصاب دانشگاه فردوسی مشهد از اردیبهشت 1396 تا مهر 1397 انجام شد. به منظور تهیه داربست، موش های صحرایی با تزریق داخل صفاقی کلرال هیدرات 10% بیهوش شدند. قطعات عصب سیاتیک موش های صحرایی در بالاتر از محل سه شاخه شدن عصب برداشته شد و پس از پاکسازی بافت های زائد به روش ساندل سلول زدایی شدند. سپس داربست های سلول زدایی شده از نظر بافتی و مکانیکی مورد ارزیابی قرار گرفت.
    یافته ها
    بررسی نتایج حاصل از ارزیابی های بافتی نشان داد که سلول زدایی داربست ها به طور کامل انجام شده است. این نتایج توسط رنگ آمیزی هماتوکسیلین-ائوزین و دپی اثبات شد. ارزیابی های تخصصی بافتی با رنگ آمیزی پیکروفوشین و بررسی میکروسکوپ الکترونی نشان داد که رشته های کلاژن و الاستین در ماتریکس خارج سلولی به طور نسبی حفظ شده اند. همچنین بررسی مکانیکی داربست ها در تست کششی نشان دهنده حفظ نسبی ماتریکس خارج سلولی داربست ها در مقایسه با گروه کنترل بود.
    نتیجه گیری
    در مجموع نتایج حاصل از این پژوهش نشان داد که داربست های حاصل از سلول زدایی با حفظ ترکیبات اصلی بافت مورد نظر می توانند بستر مناسبی برای بررسی رفتارهای سلولی باشند.
    کلید واژگان: ماتریکس خارج سلولی, اعصاب محیطی, ترمیم, عصب سیاتیک, مهندسی بافت, داربست سلولی
    Arash Abdolmaleki*, Mohammad, Bagher Ghayour, Saber Zahri, Asadollah Asadi, Morteza Behnam, Rassouli
    Background
    Tissue engineering is a developing multidisciplinary and interdisciplinary field involving the use of bioartificial implants for tissue remodeling with the target for repair and enhancing tissue or organ function. Acellular nerve has been used in experimental models as a peripheral nerve substitute. The purpose of the present study was to evaluate the mechanical and histological characteristics of acellular nerve scaffolds compared to the fresh nerve for application in environmental nerve repair.
    Methods
    This experimental study was conducted in Ferdowsi University of Mashhad Regeneration Research Laboratory, Mashhad, Iran, from May 2017 to October 2018. In this study for preparing the scaffold. The rats were sacrificed by intraperitoneal anesthesia with 10 % Chloral Hydrate solution. Then sciatic nerve fragments of the rats were removed above the nerve branching site and after cleansing of the tissues were decellularized by Sondell method, briefly nerves were treated with a series of detergent baths consisting of distilled water for 8 h, Triton X-100 for 12 h, and sodium deoxycholate for 24 hours according to the Sondell protocol. All acellularization steps were performed at room temperature. Then decellularized scaffolds were evaluated histologically and mechanically.
    Results
    The results of tissue evaluations showed that decellularization of scaffolds were done completely, this was demonstrated by hematoxylin and eosin staining and DAPI staining. Also the specialized tissue evaluations by picro-fuchsin staining and evaluation the scaffolds by scanning electron microscopy (SEM) micrographs showed that the collagen and elastin strands are relatively preserved in the extracellular matrix in comparison with control groups. As well as mechanical examination of scaffolds in tensile test showed that extracellular matrix of scaffolds was relatively preserved the main components of tissue compared to control group and scaffolds have good mechanical resistance quality for use in tissue engineering.
    Conclusion
    The results of the present study showed that decellularized scaffolds that prepared with Sondell decellularization method by preserving the main components of the tissue can be a good platform for investigating cellular behaviors.
    Keywords: extracellular matrix, peripheral nerves, regeneration, sciatic nerve, tissue engineering, tissue scaffolds
  • Mahboubeh Jafarkhani, Zeinab Salehi, Amir Aidun, Mohammad Ali Shokrgozar *
    Three-dimensional (3D) printing technology has revolutionized tissue engineering field because of its excellent potential of accurately positioning cell-laden constructs. One of the main challenges in the formation of functional engineered tissues is the lack of an efficient and extensive network of microvessels to support cell viability. By printing vascular cells and appropriate biomaterials, the 3D printing could closely mimic in vivo conditions to generate blood vessels. In vascular tissue engineering, many various approaches of 3D printing have been developed, including selective laser sintering and extrusion methods, etc. The 3D printing is going to be the integral part of tissue engineering approaches; in comparison with other scaffolding techniques, 3D printing has two major merits: automation and high cell density. Undoubtedly, the application of 3D printing in vascular tissue engineering will be extended if its resolution, printing speed, and available materials can be improved.
    Keywords: Neovascularization, Three-dimensional printings, Tissue engineering, Tissue scaffolds
  • محسن شیخ حسن، مهدیه سادات قیاثی *
    فرآیند بازسازی آسیب های عضلانی-اسکلتی (ارتوپدی)، به دلیل توانایی خودنوزایی ذاتی بسیار ضعیف بافت بالغ غضروفی، باعث ایجاد مشکلاتی در زمینه پزشکی شده است. بنابراین، پژوهش هایی بر روی گسترش استراتژی های نوین بازساختی با استفاده از ترکیب نمودن کندروسیت ها یا سلول های بنیادی با داربست ها و فاکتورهای رشد با هدف حل این مشکلات تمرکز یافته است. به دلیل قابلیت تکثیری به نسبت پایین کندروسیت های پیوند شده، مدل های جدید ساخت غضروف، استفاده از سلول های بنیادی مشتق از چربی را تحت بررسی قرار داده اند. سلول های بنیادی مشتق از چربی به راحتی بدون هیچ گونه عوارض جدی قابل دسترس بوده و قدرت تمایزی به چندین رده سلولی شامل تمایز خود به خودی به غضروف را زمانی که در داربست های ژلی همچون کلاژن به دام انداخته می شود دارا می باشد. همچنین، مطالعات اخیر برخی از مکانیسم های دخیل در فرآیند ساخت غضروف سلول های بنیادی مشتق از چربی را در شرایط آزمایشگاهی و همچنین قابلیت ترمیمی آن ها را در داربست های مهندسی شده زیستی و در حضور فاکتورهای رشد نشان داده است. افزون براین، نقش مهم مولکول های mRNA کوچک غیر کد کننده (miRNAs)، در فرآیند تمایز سلول های بنیادی مزانشیمی به رده غضروفی مشخص شده است. به طوری که طی مطالعات مختلف، تاثیر چندین miRNAs بر روی تنظیم فرآیند تمایز به غضروف سلول های بنیادی مشتق از چربی تایید شده است. در این مقاله مروری، به بررسی پیشرفت های صورت پذیرفته در زمینه استفاده از سلول های بنیادی مشتق از چربی در بازسازی غضروف پرداخته خواهد شد.
    کلید واژگان: ساخت غضروف, سلول های بنیادی, داربست های بافت
    Mohsen Sheykhhasan, Mahdieh Sadat Ghiasi *
    The cartilage is a connective tissue that, due to the strength of its extracellular matrix, allows the tissue to tolerate mechanical stress without undergoing permanent deformation. It is responsible for the support of soft tissues and due to its smooth surface and elasticity, gives the joints the ability to slip and bend. excessive weight, excessive activity, or trauma can all cause cartilage to injury. The injury can lead to swelling, pain and varying degrees of mobility loss. The process of repairing musculoskeletal (orthopedic) injuries has led to problems in the medical field, which can be attributed to the inherent weakness of adult cartilage tissue. Therefore, this necessitates research focused on the development of a new restructuring strategy by combining chondrocytes or stem cells with scaffolds and growth factors to address these problems. Correspondingly, the recent tissue engineering strategies strongly support the simultaneous use of stem cells, scaffolds and growth factors. It has also been observed that due to the relatively low proliferation of transplanted chondrocytes, new cartilage models construction have examined the use of adipose-derived stem cells. Mature adipose tissue is produced as an important source of multi-functional stem cells that can be easily separated from the stromal vascular fraction (SVF) by adipose liposuction digestion. The adipose-derived stem cells are easily accessible without any serious complications and have the power to differentiate into several cell lines, including chondrocytes as well as, they evidence self-renewal when trapped in gel scaffolds such as collagen. Also, recent studies demonstrate some of the mechanisms involved in the process of making cartilage of adipose-derived stem cells in vitro and their restorative ability in bio-engineered scaffolds in the presence of growth factors. In addition, the important role of non-encoding mRNA molecules (miRNAs) has been identified in the process of chondrogenic differentiation of adipose-derived stem cells. Furthermore, in several studies, the effect of several miRNAs has been confirmed on the regulation of the cartilage differentiation of the adipose-derived stem cells and has also been associated with effective results. In this article, we will present an overview of the advance in adipose-derived stem cells application in cartilage regeneration.
    Keywords: chondrogenesis, stem cells, tissue scaffolds
  • Madu Ghana Shyam Prasad*, Juvva Ramakrishna, Duvvi Naveen Babu
    Stem cells are the pluripotent cells that have the capacity to differentiate into other specialized cells. Recently, many experiments have been conducted to study the potentiality of stem cells in the tissue regeneration. We report two cases treated utilizing stem cells from human exfoliated deciduous teeth (SHED) in the management of periapical lesions in permanent teeth. Two normal human deciduous teeth from children, 7‒8 years of age, were collected to isolate stem cells. Two patients, one with periapical pathology alone and the other with periapical lesion along with an open apex in young permanent teeth, were selected for the study. After initial debridement of the root canals, homing of SHED was carried out and the access cavity was sealed using glass-ionomer cement. Clinical examination after 7 days, 30 days, 90 days, 180 days and 365 days revealed no symptoms. Closure of open apex and periapical tissue healing were observed radiographically at one-month review and maintained until 365-day review. Positive response to electric pulp testing was recorded for the treated teeth from the 3- to 12-month follow-ups. The treated cases demonstrated complete resolution of periapical radiolucency in a span of 30 days, which was faster than the conventional methods. SHED could be considred effective in treating the periapical lesions and open apex in permanent teeth.
    Keywords: Periapical lesions, permanent teeth, pulp necrosis, bioglass, stem cells, tissue scaffolds
  • محمد جواد فاطمی*، شیرین چهرودی، توران باقری، سحر صالح، امیر آتشی، محسن صابری، سید ابوذر حسینی، شیرین عراقی
    زمینه و هدف
    سلول های بنیادی با یا بدون داربست حمل کننده این سلول ها به عنوان روش های جدید در درمان زخم های حاد و مزمن مطرح شده اند. مطالعه حاضر با هدف بررسی امکان استفاده از نانوفیبرهای پلی اترسولفون به عنوان اسکافولد نگهدارنده سلول های بنیادی با منشا چربی با یا بدون فاکتور رشد در ترمیم زخم تمام ضخامت در رت انجام شد.
    روش بررسی
    این مطالعه تجربی در تیرماه 1392 در آزمایشگاه حیوانات بیمارستان حضرت فاطمه (س) تهران انجام شد. 48 رت به صورت تصادفی به چهار گروه تقسیم شدند. پس از ایجاد زخم در سطح خلفی رت ها، پوشش زخم در گروه اول با پلی اترسولفون (PES) همراه سلول های بنیادی چربی (ASC) و فاکتور رشد (GF)، در گروه دوم با پلی اترسولفون همراه سلول های بنیادی چربی (ASC)، در گروه سوم با پلی اترسولفون به تنهایی، در گروه چهارم (کنترل) با گاز وازلین انجام شد. سپس در روزهای 20 و 35 با فتوگرافی وسعت زخم و سرعت ترمیم و همچنین در روزهای 20 و 45 با نمونه برداری مشخصات هیستوپاتولوژی نمونه ها بررسی شد.
    یافته ها
    نتایج سرعت ترمیم زخم در گروه کنترل به طور معناداری بهتر بود (001/0P=، 013/0P=، 008/0P=). در بررسی خصوصیات هیستوپاتولوژیک نیز گروه کنترل در روز 20 به طور معناداری نتایج بهتری داشت (001/0P<) و اما در روز 45 نتایج در پارامترهای متفاوت یکسان نبود.
    نتیجه گیری
    داربست پلی اتر سولفون به تنهایی یا همراه سلول های بنیادی برگرفته از چربی نتوانست ترمیم زخم را بهبود بخشد. همچنین اضافه شدن فاکتور رشد VEGF نتوانست تغییر واضحی در ترمیم زخم ایجاد کند.
    کلید واژگان: پلی اترسولفون, نانوفایبر, اسکافولد, سلول های بنیادی, فاکتور رشد
    Mohammd Javad Fatemi*, Shirin Chehroudi, Tooran Bagheri, Sahar Saleh, Amir Atashi, Mohsen Saberi, Seyed Aboozar Hoseini, Shirin Araghi
    Background
    Acute and chronic wound healing has always been problematic. Stem cells with or without the scaffold carrying these cells have been proposed as new methods in the treatment of wounds. In this case study we have tried to examine the effect of scaffold made of polyether sulfone (PES) alone, with stem cells and along with stem cell and growth factor on wound healing in rats.
    Methods
    This experimental study was conducted in Animal Laboratory of Hazrat Fatemeh Hospital in 2012. In this study, 48 rats were randomly divided into four groups. A wound created on the back of each rat at the size of 3×3 cm. The surface of the wound in the first group is covered with PES seeded with adipose-derived stem cell (ASC) and growth factor (GF), in the second group with polyether Sulfone seeded with ASC, in the third group only with PEWS, and in the fourth group (control) with Vaseline gauze. On 20th and 35th days, the surface of the wound was assessed by photography in order to understand the process of healing. In addition, on days 20 and 45, the histopathology characteristics of the samples were studied with a biopsy of the wounds.
    Results
    The Results of wound healing in the control group was better than the other groups and its statistical difference between others was meaningful. (P=0.008, P=0.013, P=0.001) On day 20, by examining histopathological characteristics including epithelialization, the number of inflammatory cells, the amount of angiogenesis and collagen synthesis in control group, we gained better results. (P=0.000), But on day 45, the results in different parameters were not equal.
    Conclusion
    polyether sulfone scaffold alone or with adipose-derived stem cells couldn’t improve the process of wound healing. Also adding vascular endothelial growth factor (VEGF) did not change the results significantly.
    Keywords: growth factor, nanofibers, polyether sulfone, stem cells, tissue scaffolds
  • شیما توکل، هادی علیقلی، آرزو اسحق آبادی، سید مصطفی مدرس موسوی، جعفر آی، سید مهدی رضایت*
    مقدمه
    صدمه نخاعی یک وضعیت ناتوان کننده خطرناک است که می تواند منجر به فلج شدن گردد. به علت اثرات سودمند هیدروژل در مقایسه با داربست های از پیش ساخته شده، در این مطالعه یک زیست ماده بر پایه هیدروژل به نام ماتریژل به کار برده شد. ماتریژل یک زیست ماده حساس به حرارت است که در دمای بالای 20 درجه سانتی گراد تشکیل هیدروژل و نانوفیبر می دهد. ماتریژل حاوی لامینین، نیدوژن و برخی از فاکتورهای رشد است که تمایز نورونی را القاء می کند.
    مواد و روش‏ها: یک کوفتگی متوسط در طناب نخاعی در موش صحرایی بالغ ایجاد شد و ده روز پس از ضایعه، ماتریژل در محل ضایعه کاشته شد. سپس به مدت 42 روز تست Basso، Beattie، Bresnahan انجام شد. رنگ آمیزی کریزل ویوله جهت آنالیز هیستوپاتولوژی انجام شد.
    یافته ها
    داده ها بر کاهش التهاب و تعداد سلول های تیره در گروه ماتریژل در مقایسه با گروه کنترل دلالت می کند. نتایج آزمون حرکتی نشان داد که عملکرد حرکتی به طور چشمگیری در گروه حاوی ماتریژل بهبود یافته است.
    نتیجه گیری
    نتایج ما پیشنهاد می‏کند که ماتریژل به واسطه برخی از فاکتورهای رشد و مولکول های چسبنده، ممکن است اثرات مناسبی در بهبود عملکردی متعاقب ضایعه نخاعی داشته باشد.
    کلید واژگان: ضایعات طناب نخاعی, هیدروژل, لامینین, داربست بافت
    Shima Tavakol, Hadi Aligholi, Arezou Eshaghabadi, Mostafa Modarres Mousavi, Jafar Ai, Mehdi Rezayat*
    Introduction
    Spinal cord injury (SCI) is a serious disabling condition associated with paralysis. Owing to suitable effects of hydrogels compared to preformed scaffolds, in this study a hydrogel based biomaterial, Matrigel, was applied. Matrigel is a termogel that forms nanofibers and hydrogel above 20°C. It contains laminin, nidogen and some growth factors that induce neural differentiation.
    Materials And Methods
    A moderate spinal cord contusion was performed in adult rats and 10 days after injury, matrigel was implanted. Then, they follow up via Basso, Beattie, Bresnahan test for 42 days. Cresyl violet staining was performed as a histopatological analysis.
    Results
    Our data indicated less inflammation and dark cells in Matrigel group compared to control group. Locomotor test showed significant improvement of motor recovery in Matrigel group.
    Conclusion
    Our results suggest that Matrigel via some growth factors and adhesive molecules may have beneficial effects on functional recovery in SCI.
    Keywords: Spinal Cord Injuries, Hydrogels, Laminin, Tissue Scaffolds
  • کشت سه بعدی سلول های استخوانی فک انسان در داربست PLLA/HA
    جواد فاریابی، سیدنورالدین نعمت اللهی، پروین صالحی نژاد، محبوبه شاهرخی، محمدتقی خراسانی
    مقدمه
    تولید بافت استخوانی جدید با سلول و ماتریکس های خارج سلولی سنتتیک (داربست ها) روشی جدید برای بازسازی بافت های معدنی و استخوان می باشد. این مطالعه به منظور بررسی قابلیت انجام کشت سه بعدی سلول های استئوبلاست در داربست های PLLA/HA (poly L-Lactic acid/hydroxyl apatite) انجام شد.
    روش
    در این مطالعه سه نمونه استخوانی از محل جراحی دندان های عقل نهفته افراد داوطلب برداشته شد. سلول های استئوبلاست با استفاده از دو آنزیم تریپسین و کلاژناز از نمونه ها استحصال و تا پاساژ چهارم به صورت تک لایه کشت داده شده و سپس به تعداد یک میلیون سلول در میلی لیتر به داربست PLLA/HA منتقل شدند و بعد از 21 روز داربست ها توسط رنگ آمیزی های H&E، Von kossa و Hoechst و میکروسکوپ الکترونی بررسی شدند.
    یافته ها
    نتایج حاصل از مقایسه دو آنزیم تریپسین و کلاژناز نشان داد که سرعت رشد سلولی در سلول های جداشده با کلاژناز بیشتر بود. بررسی میکروسکوپ الکترونی هم چسبندگی و تکثیر سلولی را در داربست ها نشان داد. رنگ آمیزی H&E، Hoechst و Von kossa نیز حضور سلول ها در داربست ها را تایید کرد.
    نتیجه گیری
    این یافته ها تایید می کنند که سلول های استئوبلاست می توانند در شرایط آزمایشگاهی در داربست های PLLA/HA رشد کنند.
    کلید واژگان: استئوبلاست, مهندسی بافت, پلیمر PLLA, هیدورکسی آپاتیت, داربست بافتی
    Three Dimensional Culturing of Human Jaw Osteoblasts in PLLA/HA Scaffold
    Azmandian J., Rahimi N., Sohrevardi S.M., Etminan A., Fazeli F., Azizishoul S., Shafii Z
    Background and Aims
    Tissue engineering using somatic cells and synthetic extracellular matrix (scaffold) represents a new approach for regeneration of mineralized tissue and bone. This study was carried out to investigate the ability of a PLLA/HA scaffold to culture osteoblast cells in a three dimensional milieu.
    Method
    Three bony samples were taken from extraction sites during surgical extraction of wisdom teeth. Osteoblasts were obtained from specimens by using trypsin and collagenase and were cultured in monolayer up to passage four. Cells were seeded on PLLA/HA scaffolds at density of 106 cells/ml and then incubated for 21 days. The seeded cells were evaluated by Hoechst، von kossa and H&E stainings and scanning electron microscopy.
    Results
    Cellular growth was more pronounced when isolation was carried out by collagenase. According to scanning electron microscopy، osteoblast cells had been proliferated and attached to the scaffolds. H&E، Hoechst and von kossa stainings confirmed the presence of the harvested cells in the scaffold too.
    Conclusion
    Our findings suggest that osteoblast cells can grow onto PLLA/HA scaffold in vitro.
    Keywords: Osteoblasts, Tissue engineering, PLLA Polymer, Hydroxyapatite, Tissue scaffolds
  • A. Salimi, M. Ghollasi, N. Saki, F. Rahim, A. Dehghanifard, Sh Alizadeh, M. Farshdousti Hagh, M. Soleimani
    Stem cell research has obtained much prominence in recent years for its therapeutic potential in dealing with serious diseases, many of which are essentially incurable by routine therapies. Mesenchymal stem cells with pluripotency and immunomodulatory properties are suitable candidates for tissue engineering and regenerative medicine. Today, nanofibrous scaffolds are widely used in tissue engineering to improve implantation, function, proliferation and infiltration of the cells. In this regard, porous and biodegradable scaffolds with microstructure and suitable physicalmechanical properties are prepared. We review the application of mesenchymal stem cells nanoscaffolds and in tissue engineering.
    Keywords: Mesenchymal stem cells, tissue engineering, tissue scaffolds
نکته
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