The Shraga Segal Department Microbiology, Immunology and Genetics, Beer-Sheva, Israel.
The Center of Advanced Research and Education in Reproduction (CARER), Beer-Sheva, Israel.
Biofabrication. 2022 Apr 20;14(3). doi: 10.1088/1758-5090/ac6126.
This research presents a novel testis-on-a-chip (ToC) platform. Testicular cells are enzymatically isolated from the seminiferous tubules of sexually immature mice, seeded in a methylcellulose gel and cultured in a microfluidic chip. The unique design sandwiches the soft methylcellulose between stiffer agar support gels. The cells develop into spheroids continuing to proliferate and differentiate. After seven weeks of culture the cells have over 95% viability. Confocal microscopy of the developed spheroids reveals a structure containing the various stages of spermatogenesis up to and including meiosis II: premeiotic, meiotic and post-meiotic germ cells. The spheroid structure also contains the supporting Sertoli and peritubular cells. The responsiveness of the system to the addition of testosterone and retinoic acid to the culture medium during the experiment was also investigated. As a benchmark, the ToC is compared to a conventional three-dimensional methylcellulose cell culture system in a well plate. Analysis via fluorescence-activated cell sorting shows more haploid cells in the chip as compared to the plates. Immunofluorescence staining after seven weeks of culture shows more differentiated cells in the chip as compared to the well plate. This demonstrates the feasibility of our platform as well as its advantages. This research opens new horizons for the study and realization of spermatogenesis. It can also enable the implementation of microfluidic technologies in future therapeutic strategies for pre-pubertal male fertility preservation and adults with maturation arrest. Lastly, it can serve as a platform for drug and toxin testing.
本研究提出了一种新颖的睾丸芯片(Testis-on-a-Chip,ToC)平台。从未成熟雄性小鼠的曲细精管中通过酶解分离睾丸细胞,将其播种在甲基纤维素凝胶中,并在微流控芯片中培养。独特的设计将软质甲基纤维素夹在较硬的琼脂支撑凝胶之间。细胞发育成继续增殖和分化的球体。培养七周后,细胞的存活率超过 95%。对发育成的球体进行共聚焦显微镜检查,揭示了一个包含从减数分裂前期到减数分裂 II 期的各种精发生殖阶段的结构:减数前期、减数分裂和减数分裂后生殖细胞。球体结构还包含支持性的 Sertoli 细胞和管周细胞。在实验过程中,还研究了向培养基中添加睾酮和维甲酸对系统的响应。作为基准,将 ToC 与传统的三维甲基纤维素细胞培养板进行了比较。通过荧光激活细胞分选分析显示,与培养板相比,芯片中的单倍体细胞更多。培养七周后的免疫荧光染色显示,与培养板相比,芯片中的分化细胞更多。这证明了我们的平台的可行性及其优势。本研究为精发生殖的研究和实现开辟了新的视野。它还可以使微流控技术在未来的未成年男性生育力保存和成熟停滞的成年男性治疗策略中得到应用。最后,它可以作为药物和毒素测试的平台。