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Effect of KnockOut serum replacement on germ cell development of immature testis tissue culture

机译:敲除血清对未成熟睾丸组织培养生殖细胞发育的影响

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摘要

To compare KnockOut serum replacement (KSR) and fetal bovine serum (FBS) for the development of germ cells. Testicular tissues from Sprague-Dawley rats were cultured for 4 weeks in culture media supplemented with FBS or KSR. Tissue area was measured at the beginning and end of the culturing period. Testicular histology, development of the germ cells, and the diameter of seminiferous tubules were analyzed by hematoxylin and eosin staining. After 4 weeks in culture, apoptosis and expression of the stage-specific spermatogenesis marker genes Kit, Sycp3, and Crispl were assayed. Tissues cultured in KSR-supplemented media were able to sustain growth and gradually increase seminiferous tubule diameter during the culture period. In addition, spermatogonia, primary spermatocytes, secondary spermatocytes, and round spermatids were observed after 4 weeks in culture, and reverse transcription-PCR confirmed expression of the marker genes. In comparison, tissues cultured in FBS-supplemented media showed dwindling testicular organization, necrotic seminiferous tubules, and expression of Kit, but inconsistent expression of Sycp3 and Crispl KnockOut serum replacement outperforms FBS as a growth media supplements for culturing immature spermatogonial tissue culture. (C) 2016 Elsevier Inc. All rights reserved.
机译:为了比较KnockOut血清替代品(KSR)和胎牛血清(FBS)生殖细胞的发育。将来自Sprague-Dawley大鼠的睾丸组织在补充有FBS或KSR的培养基中培养4周。在培养期的开始和结束时测量组织面积。用苏木精和曙红染色分析睾丸的组织学,生殖细胞的发育以及曲细精管的直径。培养4周后,测定细胞凋亡和阶段特异性精子发生标记基因Kit,Sycp3和Crisp1的表达。在补充KSR的培养基中培养的组织能够在培养期间维持生长并逐渐增加生精小管的直径。此外,在培养4周后观察到精原细胞,原代精母细胞,继代精母细胞和圆形精子,逆转录PCR证实了标记基因的表达。相比之下,在补充FBS的培养基中培养的组织显示出睾丸组织减少,坏死的生精小管和Kit的表达,但Sycp3和Crispl KnockOut血清替代物的表达不一致,优于FBS作为用于培养未成熟的精原组织培养的生长培养基补充剂。 (C)2016 Elsevier Inc.保留所有权利。

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