In Vitro and In Vivo Determinations of The Anti-GDNF Family Receptor Alpha 1 Antibody in Mice Immunochemistry and RT-PCR

被引:11
作者
Azizi, Hossein [1 ]
Tabar, Amirreza Niazi [1 ]
Skutella, Thomas [2 ]
Govahi, Mostafa [1 ]
机构
[1] Amol Univ Special Modern Technol, Fac Biotechnol, POB 46168-49767, Amol, Iran
[2] Heidelberg Univ, Med Fac, Inst Anat & Cell Biol, Heidelberg, Germany
关键词
Analysis; Embryonic Stem Cells; GFRa1; Pluripotent Stem Cells; STEM-CELLS; EXPRESSION; PLZF;
D O I
10.22074/ijfs.2020.6051
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Background: The glial cell-derived neurotrophic factor (GDNF) family plays essential roles in the maintenance, growth regulatory and signalling pathways of sperniatogonial stem cells (SSCs). In this study, we analysed the expression of anti-GDNF family receptor alpha 1 antibody (GFRa1) by immunohistochemishy (IHC), immunocytochemistry (ICC), Fluidigm real-time polymerase chain reaction (RT-PCR) and flow cytometry analyses. Materials and Methods: In this experiment study, ICC, IHC, Fluidigm RT-PCR and flow cytometry were used to analyse the expression of the germ cell marker GFRal in testis tissue and SSC culture. Results: IHC analysis showed that there were two groups of Gl'Ital positive cells in the seminiferous tubules based on their location and expression shape - a small round punctuated shape on the basal compartment donut shape and a C-shaped expression located between the basal and the luminal compartments of the seminiferous tubules. OCT4 and PLZF positive cells may have similar patterns of expression as the first group. Assessment of the seminiferous tubule sections demonstrated that about 27% of the SSCs were positive for GFRa1. Fluidigm RT-PCR confirmed the significant expression (P<0.001) of GFRa1 in the SSCs compared to testicular stromal cells (TSCs). Flow cytometry analysis demonstrated that about 75% of the isolated SSCs colonies were positive for GFRa1. Conclusion: The results indicated that GFRa1 had a specific expression pattern both in vivo and in vitro. This finding could be helpful for understanding the proliferation, maintenance and signalling pathways of SSCs, and differentiation of meiotic and haploid germ cells.
引用
收藏
页码:228 / 233
页数:6
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