capability of cartilage extract to in vitro differentiation of rat mesenchymal stem cells (mscs) to chondrocyte lineage

نویسندگان

setareh talakoob department of biology, faculty of biological sciences, north branch of islamic azad university of tehran, tehran, iran.سازمان اصلی تایید شده: دانشگاه آزاد اسلامی علوم و تحقیقات (islamic azad university science and research branch)

mohammad taghi joghataei cellular and molecular research center, iran university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی ایران (iran university of medical sciences)

kazem parivar department of biology, faculty of basic sciences, sciences and researches branch of islamic azad university of tehran, tehran, iran.سازمان اصلی تایید شده: دانشگاه آزاد اسلامی علوم و تحقیقات (islamic azad university science and research branch)

maryam bananej department of biology, faculty of biological sciences, north branch of islamic azad university of tehran, tehran, iran.سازمان اصلی تایید شده: دانشگاه آزاد اسلامی علوم و تحقیقات (islamic azad university science and research branch)

چکیده

the importance of mesenchymal stem cells (mscs), as adult stem cells (ascs) able to divide into a variety of different cells is of utmost importance for stem cell researches. in this study, the ability of cartilage extract to induce differentiation of rat derived omentum tissue mscs (rot-mscs) into chondrocyte cells (ccs) was investigated. after isolation of rot-mscs, they were co-cultured with different concentrations of hyaline cartilage extract and chondrocyte differentiation was monitored. expression of mscs markers was analyzed via flow cytometry. moreover, expression of octamer- binding transcription factor-4 (oct-4), wilm's tumor suppressor gene-1 (wt-1), aggreacan (ag), collagen type-ii (ct-ii) and collagen type-x (ct-x) was analyzed using rt-pcr on 16, 18 and 21 days. furthermore, immunocytochemistry and western blot were performed for ct-ii production. finally, proteoglycans (pgs) were examined using toluidine blue and alcian blue staining. the phenotypic characterization revealed the positive expression of cd90, cd44 and negative expression of cd45 inrot-mscs. these cells also expressed mrna of oct-4 and wt-1 as markers of omentum tissue. differentiated rot-mscs in the presence of 20 µg/ ml cartilage extract expressed ag, ct-ii, ct-x, and pgs as specific markers of ccs. these observations suggest that cartilage extract is potentially able to induce differentiation of mscs into chondrocyte lineage and may be considered as an available source for imposing tissue healing on the damaged cartilage. more investigations are needed to prove in vivo cartilage repair via cartilage extract or its effective factors.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Capability of Cartilage Extract to In Vitro Differentiation of Rat Mesenchymal Stem Cells (MSCs) to Chondrocyte Lineage

The importance of mesenchymal stem cells (MSCs), as adult stem cells (ASCs) able to divide into a variety of different cells is of utmost importance for stem cell researches. In this study, the ability of cartilage extract to induce differentiation of rat derived omentum tissue MSCs (rOT-MSCs) into chondrocyte cells (CCs) was investigated. After isolation of rOT-MSCs, they were co-cultured with...

متن کامل

Capability of Cartilage Extract to In Vitro Differentiation of Rat Mesenchymal Stem Cells (MSCs) to Chondrocyte Lineage

The importance of mesenchymal stem cells (MSCs), as adult stem cells (ASCs) able to divide into a variety of different cells is of utmost importance for stem cell researches. In this study, the ability of cartilage extract to induce differentiation of rat derived omentum tissue MSCs (rOT-MSCs) into chondrocyte cells (CCs) was investigated. After isolation of rOT-MSCs, they were co-cultured with...

متن کامل

In vitro differentiation of rat mesenchymal stem cells to hepatocyte lineage

Objective(s): Mesenchyme is a type of undifferentiated loose connective tissue that is derived mostly from mesoderm. Recently, mesenchymal stem cells (MSCs), as adult stem cells (ASCs) able to divide into a variety of different cells, are of utmost importance for stem cell research. In this research, ability of the liver extract to induce differentiation of rat derived omentum tissue mesenchyma...

متن کامل

in vitro differentiation of rat mesenchymal stem cells to hepatocyte lineage

objective(s): mesenchyme is a type of undifferentiated loose connective tissue that is derived mostly from mesoderm. recently, mesenchymal stem cells (mscs), as adult stem cells (ascs) able to divide into a variety of different cells, are of utmost importance for stem cell research. in this research, ability of the liver extract to induce differentiation of rat derived omentum tissue mesenchyma...

متن کامل

In-vitro Differentiation of Human Umbilical Cord Wharton’s Jelly Mesenchymal Stem Cells to Insulin-Producing Cells

  Background & Objective: Diabetes is a major chronic metabolic disease in the world. Islet transplantation is a way to treat diabetes. Unfortunately, this method is restricted due to graft rejection and lack of donor islets. Mesenchymal Stem Cells (MSCS) have the ability to differentiate into Insulin-Producing Cells (IPCs). In this study, Human Umbilical Mesenchymal Stem Cells (HUMSCS) were in...

متن کامل

In vitro differentiation of rat mesenchymal stem cells to hepatocyte lineage

OBJECTIVES Mesenchyme is a type of undifferentiated loose connective tissue that is derived mostly from mesoderm. Recently, mesenchymal stem cells (MSCs), as adult stem cells (ASCs) able to divide into a variety of different cells, are of utmost importance for stem cell research. In this research, ability of the liver extract to induce differentiation of rat derived omentum tissue mesenchymal s...

متن کامل

منابع من

با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید


عنوان ژورنال:
international journal of molecular and cellular medicine

جلد ۴، شماره ۱، صفحات ۹-۲۱

میزبانی شده توسط پلتفرم ابری doprax.com

copyright © 2015-2023