Stirred suspension bioreactors as a novel method to enrich germ cells from pre‐pubertal pig testis. (15th April 2015)

• Record Type: Journal Article
• Authors: Dores, C.; Rancourt, D.; Dobrinski, I.
• Is Part Of: Andrology. Volume 3:Number 3(2015)
• Page Start: 590
• Page End: 597
• Publication Date: 2015-04-15
• Subjects: animal models -- cell culture -- spermatogonia -- testis -- xenografting; Andrology -- Periodicals; 616.65
• DOI: 10.1111/andr.12031
• Languages: English
• ISSNs: 2047-2919

Abstract

Summary: To study spermatogonial stem cells the heterogeneous testicular cell population first needs to be enriched for undifferentiated spermatogonia, which contain the stem cell population. When working with non‐rodent models, this step requires working with large numbers of cells. Available cell separation methods rely on differential properties of testicular cell types such as expression of specific cell surface proteins, size, density, or differential adhesion to substrates to separate germ cells from somatic cells. The objective of this study was to develop an approach that allowed germ cell enrichment while providing efficiency of handling large cell numbers. Here, we report the use of stirred suspension bioreactors (SSB) to exploit the adhesion properties of Sertoli cells to enrich cells obtained from pre‐pubertal porcine testes for undifferentiated spermatogonia. We also compared the bioreactor approach with an established differential plating method and the combination of both: SSB followed by differential plating. After 66 h of culture, germ cell enrichment in SSBs provided 7.3 ± 1.0‐fold ( n = 9), differential plating 9.8 ± 2.4‐fold ( n = 6) and combination of both methods resulted in 9.1 ± 0.3‐fold enrichment of germ cells from the initial germ cell population ( n = 3). To document functionality of cells recovered from the bioreactor, we demonstrated that cells retained their functional ability to reassemble seminiferous tubules de novo after grafting to mouse hosts and to support spermatogenesis. These results demonstrate that the SSB allows enrichment of germ cells in a controlled and scalable environment providing an efficient method when handling large cell numbers while reducing variability owing to handling.