Derivation, Characterization and Differentiation of Buffalo (Bubalus bubalis) Amniotic Fluid Derived Stem Cells

Amniotic fluid cells (AFCs) are obtained from amnion for pre‐natal analysis and can be cultured in vitro. Heterogeneous amniotic fluid (AF) contains various cell types, and it is believed that some of these cells possess the stem cell properties. The aim of this study was to characterize these cells by phenotypical and genotypical means in buffalo. The differentiation potential of amniotic fluid stem (AFS) cells was carried out by converting these cells into neurons. The AFCs were cultured without feeder cells in DMEM containing 16% foetal bovine serum, 1% penicillin/streptomycin and 1%l‐glutamine in 5% CO2 at 38.5 ± 0.5°C in a CO2 incubator. After 6 days of culture, different types of cells viz., star shaped (62.7%), spherical without nucleus (1.9%), spherical with nucleus (26.4%), pentagonal (0.4%) and free floating/rounded cells (8.3%) were observed. Most of the cells started anchorage‐dependent growth after day 7 of the culture. Expression of Oct‐4, Sox‐2, Nanog, alkaline phosphatase, 18s rRNA, stem cell factor, cyclin A, Nestin and FGF‐5 was observed from the AFS cells in different passages with PCR amplicon of 314, 277, 317, 180, 162, 216, 421, 307 and 210 bp, respectively. During the differentiation step, at day 6, neuron‐like cells could be clearly identified and confirmed with Nestin‐specific RT‐PCR. The cells were found to have a normal karyotype at different passages. These results may contribute towards establishing non‐embryonic pluripotent stem cells for various therapeutic and reproductive biotechnological applications in the species.