A testicular microfluidic organ-on-a-chip for mimicking spermatogenic epithelium.

Yanqing Li, Haicheng Cheng, LinYan Lv, Yiren Liu, Yun Xie, Jun Chen, Xiaoyan Liang, Chunhua Deng, Xuenong Zou, Jianhua Zhou, Guihua Liu
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Abstract

The testicular spermatogenic epithelium, the fundamental functional unit of spermatogenesis, comprises Sertoli cells and a sequence of spermatogenic cells, with the Leydig cells (LCs) playing a pivotal supporting role in sperm development. In this study, we developed a microfluidic testicular organ-on-a-chip (OoC) composed of spermatogonial stem cells, Sertoli cells, and LCs. After 28 d of culture, the testicular OoC demonstrated the formation of a spermatogenic epithelial structure, with observed proliferation and differentiation of spermatogonial stem cells. Both Sertoli and LCs were noted to perform their fundamental cellular functions and engage in intercellular communication. Applying reproductive toxicity factors to testicular OoC reduced the proliferation of spermatogonia stem cell in the chip. This testicular OoC model revealed its potential for exploring physiological functions of the testicular spermatogenic epithelium and serving as a platform for pharmacological and toxicological screening.

用于模拟生精上皮的睾丸微流控器官芯片。
睾丸生精上皮是精子发生的基本功能单位,由支持细胞和一系列生精细胞组成,其中间质细胞在精子发育中起关键的支持作用。在这项研究中,我们开发了一种由精原干细胞、支持细胞和间质细胞组成的微流控睾丸器官芯片。培养28天后,睾丸芯片器官显示出生精上皮结构的形成,并观察到精子干细胞的增殖和分化。支持细胞和间质细胞都具有基本的细胞功能并参与细胞间通讯。将生殖毒性因子应用于睾丸器官芯片可降低芯片中SSC的增殖。这种睾丸器官芯片模型揭示了其探索睾丸生精上皮生理功能的潜力,并可作为药理学和毒理学筛选的平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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