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新生睾丸细胞短暂暴露于 EGF 或 GDNF 会改变再生组织。

Brief exposure of neonatal testis cells to EGF or GDNF alters the regenerated tissue.

机构信息

Department of Veterinary Biomedical Sciences, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.

出版信息

Reprod Fertil. 2022 Feb 28;3(1):39-56. doi: 10.1530/RAF-21-0057. eCollection 2022 Jan 1.

Abstract

UNLABELLED

We have previously shown that implantation of testis cell aggregates under the back skin of immunodeficient mice results in regeneration of testis tissue. We used this unique model to investigate the effects of epidermal growth factor (EGF) and glial cell-derived neurotrophic factor (GDNF) on testis cord development. Neonatal piglet testis cells were briefly (<1 h) exposed to either low (L: 0.02 μg/mL) or high (H: 2 μg/mL) doses of EGF, GDNF, or vehicle (control), before implantation in recipient mice. Randomly selected implants were removed from each mouse at 1, 2, 4, and 8 weeks post-implantation. GDNF-L implants showed increased testis cord development over time, and EGF-L implants had increased cross-sectional area. The ratio of regular cords decreased over time in EGF-H and GDNF-H implants and was replaced by a higher ratio of irregular cords in GDNF-H. EGF-L and GDNF-H implants were quickest to display rete testis-like structures. Overall, the lower dose of each growth factor was more effective than its higher dose in improving the implantation outcomes. This is the first comprehensive assessment of these key growth factors on formation (regeneration) of testis tissue.

LAY SUMMARY

In recent decades, testicular cancer rates have quadrupled in young men while sperm counts have dropped by half. Both conditions may be related to exposure of fetuses or infants to noxious substances causing disruption of normal testis development. To study the effects of any putative factor on testis development, we established an animal model of testis tissue regeneration. We collected newborn piglet testes after routine castration, used enzymes to completely dissociate testis cells, exposed the cells to two key growth factors (EGF or GDNF), and implanted the cells under the back skin of recipient mice, acting as live incubators. We then examined implant samples after 1, 2, 4, or 8 weeks and assessed testis regeneration. Overall, the high dose of each growth factor had adverse effects on the formation of normal testis. Therefore, this novel implantation model may also be used to study the effects of potentially harmful substances on testis development.

摘要

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我们之前已经表明,将睾丸细胞聚集体植入免疫缺陷小鼠的背部皮肤下会导致睾丸组织再生。我们使用这种独特的模型来研究表皮生长因子 (EGF) 和胶质细胞衍生的神经营养因子 (GDNF) 对睾丸索发育的影响。新生仔猪睾丸细胞短暂(<1 小时)暴露于低(L:0.02μg/mL)或高(H:2μg/mL)剂量的 EGF、GDNF 或载体(对照)中,然后植入受体小鼠。随机选择的植入物在植入后 1、2、4 和 8 周从每只小鼠中取出。随着时间的推移,GDNF-L 植入物显示出睾丸索发育增加,EGF-L 植入物的横截面积增加。EGF-H 和 GDNF-H 植入物中规则索的比例随时间减少,而 GDNF-H 中不规则索的比例增加。EGF-L 和 GDNF-H 植入物最快显示出 rete testis 样结构。总体而言,每种生长因子的低剂量比高剂量更有效地改善植入结果。这是首次对这些关键生长因子在睾丸组织形成(再生)方面的全面评估。

概述

近几十年来,年轻男性的睾丸癌发病率增加了四倍,而精子数量减少了一半。这两种情况都可能与胎儿或婴儿接触有害物质有关,这些有害物质会破坏正常的睾丸发育。为了研究任何假定因素对睾丸发育的影响,我们建立了睾丸组织再生的动物模型。我们在常规去势后收集新生仔猪睾丸,使用酶完全解离睾丸细胞,将细胞暴露于两种关键生长因子(EGF 或 GDNF)下,并将细胞植入受体小鼠的背部皮肤下,作为活体孵化器。然后,我们在 1、2、4 或 8 周后检查植入物样本并评估睾丸再生。总体而言,每种生长因子的高剂量都会对正常睾丸的形成产生不良影响。因此,这种新的植入模型也可用于研究潜在有害物质对睾丸发育的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08c8/9012938/185d08c5a93e/RAF-21-0057fig1.jpg

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