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冷冻保存的小牛睾丸组织的异种移植。

Xenotransplantation of Cryopreserved Calf Testicular Tissues.

作者信息

Zhao Yansen, Zhu Wenqian, Yang Rui, Zhang Boyang, Tang Bo, Zhang Xueming

机构信息

State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, College of Veterinary Medicine, Jilin University, Changchun 130062, China.

出版信息

Vet Sci. 2025 Mar 4;12(3):247. doi: 10.3390/vetsci12030247.

Abstract

The cryopreservation of testicular tissues meets the demands for the germplasm preservation of humans and animals. Previously, we reported on the cryopreservation of bovine testicular tissues. To further evaluate the viability of these tissues, subcutaneous xenotransplantation of the frozen-thawed calf testicular tissues was performed with castrated nude mice as the recipients. After 28 days (D28), the survival and development of the grafts were examined. The grafts from 1-day-old (D1) calf testes were recovered and angiogenesis around the grafts was observed. Histologically, the seminiferous cords in the grafts were well maintained and capillaries in the interstitium were observed. Quantitative real-time PCR (qRT-PCR) analysis showed that the grafts expressed germline genes , , and and somatic genes , and . The expressions of , , , and Star were higher in 28D grafts than those in 1D and 30-day-old (30D) calf testicular controls. Together, we initially demonstrate that cryopreserved calf testicular tissues retain their viability and developmental capacity after xenotransplantation.

摘要

睾丸组织的冷冻保存满足了人类和动物种质保存的需求。此前,我们报道了牛睾丸组织的冷冻保存。为了进一步评估这些组织的活力,以去势裸鼠为受体,对冻融后的犊牛睾丸组织进行了皮下异种移植。28天后(D28),检查移植物的存活和发育情况。回收了来自1日龄(D1)犊牛睾丸的移植物,并观察了移植物周围的血管生成。组织学检查显示,移植物中的生精索保存良好,间质中可见毛细血管。定量实时PCR(qRT-PCR)分析表明,移植物表达生殖系基因、和,以及体细胞基因、和。在28天的移植物中,、、和Star的表达高于1日龄和30日龄(30D)犊牛睾丸对照。总之,我们初步证明,冷冻保存的犊牛睾丸组织在异种移植后保留了其活力和发育能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d12/11946348/7efd172d97e4/vetsci-12-00247-g001.jpg

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