CREATING MENISCUS CELL POPULATION WITH MESENCHYMAL STEM CELLS AND DIFFERENTIATED CELL COCKTAIL

Abstract

Meniscus is mainly composed of three different cell types; chondrocytes(Ch) situate in the superficial zone, whereas fibroblast-like cells locate in the peripheral region having long cell extensions in contact with different parts of the matrix, fibrochondrocytes(FC), is from the inner part of the meniscus and show a clear cell associated matrix. The aim of this study is to develop meniscus cell population using with mesenchymal stem cells (MSCs). For this purpose, MSCs were isolated from rabbit bone marrow and verified by flow cytometry analyses using cell surface markers (CD73APC, CD90FITC, CD34PE, CD45PE/Cy5.5). The results indicate that CD73 and CD90-positive cells were 92.8%, and CD 45 and CD 34-negative cells were 52.4%. Differentiation potential of MSCs were also evaluated by differentiating into Ch, osteoblasts (Ob), adipocytes (Ad), fibroblasts (Fb). Histology stainings showed that differentiated Ch can produce proteoglycans, Ob have mineralization property, Fb have spindle shape and Ad have oil drops morphology. Afterwards Fb, Ch and undifferentiated MSCs (for formation of the FC) were seeded in same plate in cocktail medium and Fb, Ch, seeded individually, were used as control group. Proliferation activity of the cells was analyzed by XTT assay at 3^th,7^thand14^thdays. In addition, cells were analyzed by flow cytometry with identical surface markers at 3^th,7^thand14^thdays. Results show that cell cocktail have the greatest proliferation ability with a greater speed than the individual Ch or Fb cultures. In addition, FC formation was identified by histological staining. In conclusion, meniscus specific cell population has been successfully generated from the cell cocktail containing rabbit MSCs.