A monolayer microfluidic device supporting mouse spermatogenesis with improved visibility

作者：Yamanaka Hiroyuki; Komeya Mitsuru; Nakamura Hiroko; Sanjo Hiroyuki; Sato Takuya; Yao Masahiro; Kimura Hiroshi^*; Fujii Teruo^*; Ogawa Takehiko^*

来源：Biochemical and Biophysical Research Communications, 2018, 500(4): 885-891.

DOI：10.1016/j.bbrc.2018.04.180

• Spermatogenesis
• Organ culture
• Microfluidic device
• Spermiogenesis
• Acrosome

In our previous study, we produced a microfluidic device (MFD) which successfully maintained spermatogenesis for over 6 months in mouse testis tissues loaded in the device. In the present study, we developed a new MFD, a monolayer device (ML-D) with a barrier structure consisting of pillars and slits, which is simpler in design and easier to make. This ML-D was also effective for inducing mouse spermatogenesis and maintained it for a longer period than the conventional culture method. In addition, we devised a way of introducing sample tissue into the device during its production, just before bonding the upper layer of polydimethylsiloxane (PDMS) and bottom glass slide. The tissue can obtain nutrients horizontally from the medium running beside it and oxygen vertically from above through PDMS. In addition, the glass slide set at the bottom improved the visibility of the sample tissue with an inverted microscope. When we took photos of cultured tissue of the Acr-Gfp transgenic mouse testis in ML-D sequentially every day, morphological changes of the acrosome during spermiogenesis were successfully recorded. The ML-D is simple in design and useful for culturing testis tissue for inducing and maintaining spermatogenesis with clearer visibility. Due to the new method of sample loading, tissues other than testis should also be applicable.

• 出版日期2018-6-12