Author/Authors :
Ahrari, Iman Student Research Committee - Shiraz University of Medical Sciences (SUMS), Shiraz, IR Iran , Purhabibi Zarandi, Nima Student Research Committee - Shiraz University of Medical Sciences (SUMS), Shiraz, IR Iran , Khosravi Maharlooei, Mohsen Student Research Committee - Shiraz University of Medical Sciences (SUMS), Shiraz, IR Iran , Monabati, Ahmad Department of Pathology - Shiraz University of Medical Sciences (SUMS), Shiraz, IR Iran , Attari, Armin Department of Cardiovascular Medicine - Shiraz University of Medical Sciences (SUMS), Shiraz, IR Iran , Ahrari, Sajjad Student Research Committee - Shiraz University of Medical Sciences (SUMS), Shiraz, IR Iran
Abstract :
Background: Mesenchymal stromal cells (MSCs) as multipotent cells with the capacity to be differentiated into several cell lineages are
promising sources for cell therapy and tissue engineering nowadays. Today most of culturing media are supplemented with fetal bovine
serum (FBS). But FBS containing culturing media may raise the possibility of zoonotic infections and immunological reactions in cell
therapy conditions. Numerous investigations have been performed to assess the use of FBS-free culturing systems for bone marrow derived
mesenchymal stromal cell isolation. Objectives: The present investigation aimed to assess the effect of serum-free media on growth and differentiating capacity of adipose tissuederived
MSCs. Materials and Methods: Approximately, 1cm3 surgically waste sterile adipose tissue was digested with collagenase-I leading to a single cell
suspension. The isolated cells were cultured in Ultra Culture media supplemented with 2% Ultroser G. MSC’s isolation was confirmed with
respect to morphology, flowcytometry, adipogenic and osteogenic differentiation potentials. Results: The isolated cells showed adherent spindle shaped morphology, expanded rapidly and revealed expected MSC flowcytometric
characteristics; they were positive for CD73, CD90, CD105, CD44, CD166, CD44 and negative for hematopoietic antigen such as CD45, CD34
and CD14. They could also be differentiated successfully into osteoblast and adipocyte, being confirmed by using Alizarin Red and Oil red O
staining, respectively. Conclusions: According to the results of the present study, it can be concluded that adipose derived MSCs can be cultured in serum-free media
with no change in their differentiating capacity. This finding gives us a hope for future cell therapy studies and trials with little concern about
zoonotic infections or immunological reaction.
Keywords :
Mesenchymal Stem Cells , Cariel , Culture Medium , Cell Therapy