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伴侣免疫基因结构的差异会增加女性生殖道内精子的活力。

Structural dissimilarity of partners' immune genes increases sperm viability in women's reproductive tract.

机构信息

Department of Environmental and Biological Sciences, University of Eastern Finland, Joensuu, Finland.

North Karelia Central Hospital, Joensuu, Finland.

出版信息

J Evol Biol. 2021 Jul;34(7):1125-1132. doi: 10.1111/jeb.13872. Epub 2021 Jun 12.

Abstract

Human leucocyte antigen (HLA) genes appear to mediate pre- and post-copulatory mate choice towards HLA-dissimilar ('compatible') partners. However, since genetically distinct alleles often have similar immunogenic properties, genetic dissimilarity is not necessarily an accurate predictor of the functional compatibility of HLA alleles and, hence, may not reflect partners' true compatibility. Furthermore, it has remained unclear whether other genes of the immune system could also play a role in male-female compatibility. We studied whether the immunoglobulin binding regions (eplets) of HLA molecules and the immunoglobulin structural dissimilarity of the partners affect their gamete-level compatibility. We exposed sperm of multiple men to follicular fluid or cervical mucus of multiple women and tested whether sperm viability in these reproductive secretions was influenced by HLA eplet and immunoglobulin structural dissimilarity between partners. We found that eplet dissimilarity positively affects sperm viability in follicular fluid, whereas immunoglobulin dissimilarity enhanced sperm viability in cervical mucus. Together, these findings indicate that structural characteristics of both HLA alleles and immunoglobulins may facilitate cryptic female choice towards immunologically compatible partners. Our results, thus, indicate that partners' genetic compatibility may have wider immunological basis than traditionally has been assumed. Relative contribution of different immunogenetic factors to overall compatibility of the reproductive partners needs to be clarified in future studies.

摘要

人类白细胞抗原(HLA)基因似乎介导了配偶选择前和选择后的伴侣选择,以寻找 HLA 不同(“相容”)的伴侣。然而,由于遗传上不同的等位基因通常具有相似的免疫原性,遗传上的差异不一定能准确预测 HLA 等位基因的功能相容性,因此,可能无法反映伴侣的真实相容性。此外,其他免疫系统基因是否也能在男性-女性相容性中发挥作用,仍不清楚。我们研究了 HLA 分子的免疫球蛋白结合区(表位)和伴侣之间的免疫球蛋白结构差异是否会影响它们的配子水平相容性。我们将多个男性的精子暴露于多个女性的卵泡液或宫颈粘液中,并测试了精子在这些生殖分泌物中的活力是否受到 HLA 表位和伴侣之间免疫球蛋白结构差异的影响。我们发现,表位差异对卵泡液中的精子活力有积极影响,而免疫球蛋白差异增强了宫颈粘液中精子的活力。这些发现表明,HLA 等位基因和免疫球蛋白的结构特征可能有助于女性对免疫相容的伴侣进行隐性选择。因此,我们的研究结果表明,伴侣的遗传相容性可能具有比传统上所假设的更广泛的免疫学基础。未来的研究需要阐明不同免疫遗传因素对生殖伴侣整体相容性的相对贡献。

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