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Regulation of blood-testis barrier assembly in vivo by germ cells.


ABSTRACT: The assembly of the blood-testis barrier (BTB) during postnatal development is crucial to support meiosis. However, the role of germ cells in BTB assembly remains unclear. Herein, KitW/KitWV mice were used as a study model. These mice were infertile, failing to establish a functional BTB to support meiosis due to c-Kit mutation. Transplantation of undifferentiated spermatogonia derived from normal mice into the testis of KitW/KitWV mice triggered functional BTB assembly, displaying cyclic remodeling during the epithelial cycle. Also, transplanted germ cells were capable of inducing Leydig cell testosterone production, which could enhance the expression of integral membrane protein claudin 3 in Sertoli cells. Early spermatocytes were shown to play a vital role in directing BTB assembly by expressing claudin 3, which likely created a transient adhesion structure to mediate BTB and cytoskeleton assembly in adjacent Sertoli cells. In summary, the positive modulation of germ cells on somatic cell function provides useful information regarding somatic-germ cell interactions.-Li, X.-Y., Zhang, Y., Wang, X.-X., Jin, C., Wang, Y.-Q., Sun, T.-C., Li, J., Tang, J.-X., Batool, A., Deng, S.-L., Chen, S.-R., Cheng, C. Y., Liu, Y.-X. Regulation of blood-testis barrier assembly in vivo by germ cells.

SUBMITTER: Li XY 

PROVIDER: S-EPMC6137450 | biostudies-literature | 2018 Mar

REPOSITORIES: biostudies-literature

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Regulation of blood-testis barrier assembly in vivo by germ cells.

Li Xiao-Yu XY   Zhang Yan Y   Wang Xiu-Xia XX   Jin Cheng C   Wang Yu-Qian YQ   Sun Tie-Cheng TC   Li Jian J   Tang Ji-Xin JX   Batool Alia A   Deng Shou-Long SL   Chen Su-Ren SR   Cheng C Yan CY   Liu Yi-Xun YX  

FASEB journal : official publication of the Federation of American Societies for Experimental Biology 20180103 3


The assembly of the blood-testis barrier (BTB) during postnatal development is crucial to support meiosis. However, the role of germ cells in BTB assembly remains unclear. Herein, Kit<sup>W</sup>/Kit<sup>WV</sup> mice were used as a study model. These mice were infertile, failing to establish a functional BTB to support meiosis due to c-Kit mutation. Transplantation of undifferentiated spermatogonia derived from normal mice into the testis of Kit<sup>W</sup>/Kit<sup>WV</sup> mice triggered funct  ...[more]

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