Differentiation of human primary testicular cells in the presence of SCF using the organoid culture system

Author:

Nikmahzar Aghbibi1,Koruji Morteza2,Jahanshahi Mehrdad3,Khadivi Farnaz4,Shabani Maryam1,Dehghani Sanaz5,Forouzesh Mehdi6,Jabari Ayob7,Feizollahi Narjes1,Salem Maryam1,Ghanami Gashti Nasrin8,Abbasi Yasaman9,Abbasi Mehdi1ORCID

Affiliation:

1. Department of Anatomy, School of Medicine Tehran University of Medical Sciences Tehran Iran

2. Stem Cell and Regenerative Medicine Center & Department of Anatomy School of Medicine, Iran University of Medical Sciences Tehran Iran

3. Neuroscience Research Center, Department of Anatomy, Faculty of Medicine Golestan University of Medical Sciences Gorgan Iran

4. Department of Anatomy, School of Medicine Shahrekord University of Medical Sciences Shahrekord Iran

5. Organ Procurement Unit, Sina Hospital Tehran University of Medical Sciences Tehran Iran

6. Legal Medicine Organization of Iran Legal Medicine Research Center, Legal Medicine Organization Tehran Iran

7. Department of Anatomy Zahedan Medical University of Science Zahedan Iran

8. Biomaterials Cluster, Bernal Institute University of Limerick Limerick Ireland

9. Program in Neuroscience, Center to Advance Chronic Pain Research, Department of Neural and Pain Sciences, School of Dentistry University of Maryland Baltimore Maryland USA

Abstract

AbstractPurposeDevelopment of organoids using human primary testicular cells has remained a challenge due to the complexity of the mammalian testicular cytoarchitecture and culture methods. In this study, we generated testicular organoids derived from human primary testicular cells. Then, we evaluated the effect of stem cell factor (SCF) on cell differentiation and apoptosis in the testicular organoid model.MethodsThe testicular cells were harvested from the three brain‐dead donors. Human spermatogonial stem cells (SSCs) were characterized using immunocytochemistry (ICC), RT‐PCR and flow cytometry. Testicular organoids were generated from primary testicular cells by hanging drop culture method and were cultured in three groups: control group, experimental group 1 (treated FSH and retinoic acid (RA)), and experimental group 2 (treated FSH, RA and SCF), for five weeks. We assessed the expression of SCP3 (Synaptonemal Complex Protein 3) as a meiotic gene, PRM2 (Protamine 2) as a post‐meiotic marker and apoptotic genes of Bax (BCL2‐Associated X Protein) and Bcl‐2 (B‐cell lymphoma 2), respectively by using RT‐qPCR. In addition, we identified the expression of PRM2 by immunohistochemistry (IHC).ResultsRelative expression of SCP3, PRM2 and Bcl‐2 were highest in group 2 after five weeks of culture. In contrast, BAX expression level was lower in experimental group 2 in comparison with other groups. IHC analyses indicated the highest expression of PRM2 as a postmeiotic marker in group 2 in comparison to 2D culture and control groups but not find significant differences between experimental group 1 and experimental group 2 groups. Morphological evaluations revealed that organoids are compact spherical structures and in the peripheral region composed of uncharacterized elongated fibroblast‐like cells.ConclusionOur findings revealed that the testicular organoid culture system promote the spermatogonial stem cell (SSC) differentiation, especially in presence of SCF. Developed organoids are capable of recapitulating many important properties of a stem cell niche.

Funder

Tehran University of Medical Sciences and Health Services

Publisher

Wiley

Subject

Biomedical Engineering,General Medicine,Biomaterials,Medicine (miscellaneous),Bioengineering

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