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Bones Morphogenic Protein-4 and Retinoic Acid Combined Treatment Comparative Analysis for in Vitro Differentiation Potential of Murine Mesenchymal Stem Cells Derived From Bone Marrow and Adipose Tissue Into Germ Cells Publisher Pubmed



Shirzeyli MH1 ; Khanlarkhani N2 ; Amidi F2 ; Shirzeyli FH3 ; Aval FS4 ; Sobhani A2
Authors
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Authors Affiliations
  1. 1. Department of Biology and Anatomical Sciences, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  2. 2. Department of Anatomical Sciences, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Department of Animal Science, Science and Research Branch, Islamic Azad University, Tehran, Iran
  4. 4. Department of Anatomical Sciences, Zahedan University of Medical Sciences, Zahedan, Iran

Source: Microscopy Research and Technique Published:2017


Abstract

Nowadays, infertility is no longer considered as an unsolvable disorder due to progresses in germ cells derived from stem lineage with diverse origins. Technical and ethical challenges push researchers to investigate various tissue sources to approach more efficient gametes. The purpose of the current study is to investigate the efficacy of a combined medium, retinoic acid (RA) together with Bone Morphogenic Protein-4 (BMP4), on differentiation of Bone Marrow Mesenchymal Stem Cells (BMMSCs) and adipose-derived mesenchymal stem cells (ADMSCs) into germ cells. Murine MSCs were obtained from both Bone Marrow (BM) and Adipose Tissue (AT) samples and were analyzed for surface markers to get further verification of their nature. BMMSCs and ADMSCs were induced into osteogenic and adipogenic lineage cells respectively, to examine their multipotency. They were finally differentiated into germ cells using media enriched with BMP4 for 4 days followed by addition of RA for 7 days (11 days in total). Analyzing of differentiation potential of BMMSCs- and ADMSCs were performed via Immunofluorescence, Flowcytometry and Real time-PCR techniques for germ cell-specific markers (Mvh, Dazl, Stra8 and Scp3). Mesenchymal surface markers (CD90 and CD44) were expressed on both BMMSCs and ADMSCs, while endothelial and hematopoietic cell markers (CD31 and CD45) had no expression. Finally, all germ-specific markers were expressed in both BM and AT. Although germ cells differentiated from ADMSCs showed faster growth and proliferation as well as easy collection, they significantly expressed germ-specific markers lower than BMMSCs. This suggests stronger differentiation potential of murine BMMSCs than ADMSCs. © 2017 Wiley Periodicals, Inc.
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