Record number :
2391805
Title of article :
Propagation of human germ stem cells in long-term culture
Author/Authors :
Akhondi، Mohammad-Mehdi نويسنده , , Mohazzab، Arash نويسنده Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR , , Jeddi Tehrani]، Mahmood نويسنده , , Sadeghi، Mohammad Reza نويسنده Monoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran. , , Eidi، Akram نويسنده Department of Biology‚ Science & Research Branch , , Khodadadi، Abbas ali نويسنده , , Piravar، Zeinab نويسنده Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran ,
Issue Information :
فصلنامه با شماره پیاپی سال 2013
Pages :
8
From page :
551
To page :
558
Abstract :
Background: Spermatogonial stem cells (SSCs), a subset of undifferentiated type A spermatogonia, are the foundation of complex process of spermatogenesis and could be propagated in vitro culture conditions for long time for germ cell transplantation and fertility preservation. Objective: The aim of this study was in vitro propagation of human spermatogonial stem cells (SSCs) and improvement of presence of human Germ Stem Cells (hGSCs) were assessed by specific markers POU domain, class 5, transcription factor 1 (POU5F1), also known as Octamer-binding transcription factor 4 (Oct-4) and PLZF (Promyelocytic leukaemia zinc finger protein). Materials and Methods: Human testicular cells were isolated by enzymatic digestion (Collagenase IV and Trypsin). Germ cells were cultured in Stem-Pro 34 media supplemented by growth factors such as glial cell line-derived neurotrophic factor, basic fibroblast growth factor, epidermal growth factor and leukemia inhibitory factor to support self-renewal divisions. Germline stem cell clusters were passaged and expanded every week. Immunofluorecent study was accomplished by Anti-Oct4 antibody through the culture. The spermatogonial stem cells genes expression, PLZF, was studied in testis tissue and germ stem cells entire the culture. Results: hGSCs clusters from a brain dead patient developed in testicular cell culture and then cultured and propagated up to 6 weeks. During the culture Oct4 were a specific marker for identification of hGSCs in testis tissue. Expression of PLZF was applied on RNA level in germ stem cells. Conclusion: hGSCs indicated by SSCs specific marker can be cultured and propagated for long-term in vitro conditions.
Journal title :
International Journal of Reproductive BioMedicine
Serial Year :
2013
Link To Document :
بازگشت