| Literature DB >> 27077675 |
Fatemeh Sadeghian-Nodoushan1, Reza Aflatoonian2, Zahra Borzouie1, Fatemeh Akyash1, Farzaneh Fesahat1, Mehrdad Soleimani3, Samaneh Aghajanpour2, Harry D Moore4, Behrouz Aflatoonian1.
Abstract
Human male germ-line stem cells (hmGSCs) and human testis-derived embryonic stem cell-like (htESC-like) cells are claimed to be in vitro pluripotent counterparts of spermatogonial stem cells (SSCs), but the origin and pluripotency of human testis-derived cell cultures are still under debate. The aim of this study was to generate putative pluripotent stem cells in vitro from human testicular sperm-extracted (TESE) samples of infertile men, and to assess their pluripotency and capacity to differentiate. TESE samples were minced, enzymatically disaggregated and dispersed into single-cell or cluster suspensions, and then cultured. Initially, cell clusters resembled those described for hmGSCs and htESC-like cells, and were positive for markers such as OCT4/POU5F1, NANOG, and TRA-2-54. Prolonged propagation of cell clusters expressing pluripotency markers did not thrive; instead, the cells that emerged possessed characteristics of mesenchymal stromal cells (MSCs) such as STRO-1, CD105/EGLN1, CD13/ANPEP, SOX9, vimentin, and fibronectin. KIT, SOX2, and CD44 were not expressed by these MSCs. The multipotential differentiation capacity of these cells was confirmed using Oil Red-O and Alizarin Red staining after induction with specific culture conditions. It is therefore concluded that pluripotent stem cells could not be derived using the conditions previously reported to be successful for TESE samples.Entities:
Mesh:
Year: 2016 PMID: 27077675 DOI: 10.1002/mrd.22620
Source DB: PubMed Journal: Mol Reprod Dev ISSN: 1040-452X Impact factor: 2.609