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促卵泡激素受体N端57氨基酸蛋白作为候选男性避孕疫苗的制备与应用

The preparation and application of N-terminal 57 amino acid protein of the follicle-stimulating hormone receptor as a candidate male contraceptive vaccine.

作者信息

Xu Cheng, Li Ying-Chun, Yang Hua, Long Yan, Chen Min-Jian, Qin Yu-Feng, Xia Yan-Kai, Song Ling, Gu Ai-Hua, Wang Xin-Ru

机构信息

State Key Laboratory of Reproductive Medicine, Institute of Toxicology; Key Laboratory of Modern Toxicology of Ministry of Education, School of Public Health, Nanjing, China, China.

出版信息

Asian J Androl. 2014 Jul-Aug;16(4):623-30. doi: 10.4103/1008-682X.125910.

DOI:10.4103/1008-682X.125910
PMID:24713829
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4104094/
Abstract

Follicle-stimulating hormone receptor (FSHR), which is expressed only on Sertoli cells and plays a key role in spermatogenesis, has been paid attention for its potential in male contraception vaccine research and development. This study introduces a method for the preparation and purification of human FSHR 57-amino acid protein (FSHR-57aa) as well as determination of its immunogenicity and antifertility effect. A recombinant pET-28a(+)-FSHR-57aa plasmid was constructed and expressed in Escherichia coli strain BL21 Star TM (DE3) and the FSHR-57aa protein was separated and collected by cutting the gel and recovering activity by efficient refolding dialysis. The protein was identified by Western blot and high-performance liquid chromatography analysis with a band of nearly 7 kDa and a purity of 97.4%. Male monkeys were immunized with rhFSHR-57aa protein and a gradual rising of specific serum IgG antibody was found which reached a plateau on day 112 (16 weeks) after the first immunization. After mating of one male with three female monkeys, the pregnancy rate of those mated with males immunized against FSHR-57aa was significantly decreased while the serum hormone levels of testosterone and estradiol were not disturbed in the control or the FSHR-57aa groups. By evaluating pathological changes in testicular histology, we found that the blood-testis barrier remained intact, in spite of some small damage to Sertoli cells. In conclusion, our study demonstrates that the rhFSHR-57aa protein might be a feasible male contraceptive which could affect sperm production without disturbing hormone levels.

摘要

卵泡刺激素受体(FSHR)仅在支持细胞上表达,在精子发生过程中起关键作用,其在男性避孕疫苗研发中的潜力已受到关注。本研究介绍了一种制备和纯化人卵泡刺激素受体57氨基酸蛋白(FSHR - 57aa)的方法,以及测定其免疫原性和抗生育效果。构建了重组pET - 28a(+) - FSHR - 57aa质粒,并在大肠杆菌BL21 Star TM (DE3)菌株中表达,通过切胶分离收集FSHR - 57aa蛋白,并通过高效重折叠透析恢复活性。通过蛋白质免疫印迹和高效液相色谱分析鉴定该蛋白,其条带近7 kDa,纯度为97.4%。用重组人FSHR - 57aa蛋白免疫雄性猴子,发现特异性血清IgG抗体逐渐升高,在首次免疫后第112天(16周)达到平台期。一只雄性猴子与三只雌性猴子交配后,与免疫FSHR - 57aa的雄性猴子交配的雌性猴子的怀孕率显著降低,而对照组和FSHR - 57aa组的血清睾酮和雌二醇激素水平未受干扰。通过评估睾丸组织学的病理变化,我们发现血睾屏障保持完整,尽管支持细胞有一些小损伤。总之,我们的研究表明重组人FSHR - 57aa蛋白可能是一种可行的男性避孕药,它可以在不干扰激素水平的情况下影响精子生成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34ac/4104094/e19de3129bfb/AJA-16-623-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34ac/4104094/bcc11d53dae2/AJA-16-623-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34ac/4104094/754b328d24a9/AJA-16-623-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34ac/4104094/d6911b404e77/AJA-16-623-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34ac/4104094/f55160e50a5f/AJA-16-623-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34ac/4104094/7a56db7c8608/AJA-16-623-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34ac/4104094/c28bdf1d317a/AJA-16-623-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34ac/4104094/1657a72e669a/AJA-16-623-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34ac/4104094/87efd7011a16/AJA-16-623-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34ac/4104094/e19de3129bfb/AJA-16-623-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34ac/4104094/bcc11d53dae2/AJA-16-623-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34ac/4104094/754b328d24a9/AJA-16-623-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34ac/4104094/d6911b404e77/AJA-16-623-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34ac/4104094/f55160e50a5f/AJA-16-623-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34ac/4104094/7a56db7c8608/AJA-16-623-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34ac/4104094/c28bdf1d317a/AJA-16-623-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34ac/4104094/1657a72e669a/AJA-16-623-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34ac/4104094/87efd7011a16/AJA-16-623-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34ac/4104094/e19de3129bfb/AJA-16-623-g012.jpg

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