Modular ۳D culture platform combining methylcellulose, testicular ECM, and Sertoli cells for in vitro spermatogenesis

سال انتشار: 1405
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 22

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شناسه ملی سند علمی:

JR_IJBMS-29-9_007

تاریخ نمایه سازی: 17 مهر 1405

چکیده مقاله:

Objective(s): We aimed to develop and characterize a ۳D culture platform combining methylcellulose (MC) with decellularized testicular extracellular matrix (ECM) and Sertoli cell co-culture to support human spermatogonial stem cell (SSC) survival and differentiation.Materials and Methods: Human testicular cells were isolated and characterized by immunofluorescence and flow cytometry. Sheep testicular tissue was decellularized using detergents and characterized by several histology techniques. ECM was solubilized and mixed with MC at various ratios to make hybrid hydrogels. Hydrogels were characterized for pore size, porosity, mechanical properties, gelation kinetics, and degradation kinetics using scanning electron microscopy, rheological analysis, turbidity analysis, and mass loss assays. Human SSCs and Sertoli cells were cultured in ۳D hydrogels for four weeks under differentiation conditions. Cell viability was assessed using the MTT assay, and gene expression of SSC, meiotic, post-meiotic, and apoptotic markers was evaluated by RT-PCR.Results: After four weeks of proliferation, PLZF-positive cells increased from ۱۹% to ۷۳%. Decellularization reduced DNA content by ۹۶% while preserving key matrix components. Hybrid hydrogels displayed interconnected porous structures with pore sizes of about ۶۵–۱۸۱ µm. All functional hydrogels supported cell viability; however, ECM-rich hydrogels significantly up-regulated PRM۲ compared to ۲D controls, indicating enhanced post-meiotic differentiation. MC-only scaffolds displayed elevated pro-apoptotic BAX expression compared to ECM-rich matrices, suggesting that bioactive ECM ligands confer cytoprotection.Conclusion: The modular MC/ECM hybrid hydrogel provides a tunable, physiologically relevant ۳D culture system that is superior to conventional approaches in supporting SSC maintenance and differentiation, offering promise for fertility preservation strategies.

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نویسندگان

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

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Urology and Nephrology Research Center, Research Institute for Urology and Nephrology, Shahid Beheshti University of Medical Sciences,Tehran, Iran

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Legal Medicine Research Center, Legal Medicine Organization, Tehran, Iran

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Infertility Department, Alavi Hospital, Ardabil University of Medical Science, Ardabil, Iran

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Department of Chemical and Petroleum Engineering, Sharif University of Technology, Tehran, Iran

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Bernal Institute and School of Engineering, University of Limerick, Limerick, Ireland

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Department of Infertility, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran

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Department of Life Science Engineering, Faculty of New Science and Technology, University of Tehran, Tehran, Iran

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Clinical Immunology Research Center, Zahedan University of Medical Sciences, Zahedan, Iran

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Medical Plants Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran

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

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Urology and Nephrology Research Center, Research Institute for Urology and Nephrology, Shahid Beheshti University of Medical Sciences,Tehran, Iran

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

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