• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

含 PYDD 的 NOD 样受体(NLRPs)在卵母细胞和早期胚胎发育中的关键作用†。

The pivotal roles of the NOD-like receptors with a PYD domain, NLRPs, in oocytes and early embryo development†.

机构信息

Department of Biomedicine, Aarhus University, Aarhus, Denmark.

Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.

出版信息

Biol Reprod. 2019 Aug 1;101(2):284-296. doi: 10.1093/biolre/ioz098.

DOI:10.1093/biolre/ioz098
PMID:31201414
Abstract

Nucleotide-binding oligomerization domain (NOD)-like receptors with a pyrin domain (PYD), NLRPs, are pattern recognition receptors, well recognized for their important roles in innate immunity and apoptosis. However, several NLRPs have received attention for their new, specialized roles as maternally contributed genes important in reproduction and embryo development. Several NLRPs have been shown to be specifically expressed in oocytes and preimplantation embryos. Interestingly, and in line with divergent functions, NLRP genes reveal a complex evolutionary divergence. The most pronounced difference is the human-specific NLRP7 gene, not identified in rodents. However, mouse models have been extensively used to study maternally contributed NLRPs. The NLRP2 and NLRP5 proteins are components of the subcortical maternal complex (SCMC), which was recently identified as essential for mouse preimplantation development. The SCMC integrates multiple proteins, including KHDC3L, NLRP5, TLE6, OOEP, NLRP2, and PADI6. The NLRP5 (also known as MATER) has been extensively studied. In humans, inactivating variants in specific NLRP genes in the mother are associated with distinct phenotypes in the offspring, such as biparental hydatidiform moles (BiHMs) and preterm birth. Maternal-effect recessive mutations in KHDC3L and NLRP5 (and NLRP7) are associated with reduced reproductive outcomes, BiHM, and broad multilocus imprinting perturbations. The precise mechanisms of NLRPs are unknown, but research strongly indicates their pivotal roles in the establishment of genomic imprints and post-zygotic methylation maintenance, among other processes. Challenges for the future include translations of findings from the mouse model into human contexts and implementation in therapies and clinical fertility management.

摘要

核苷酸结合寡聚化结构域 (NOD)-样受体含有一个吡咯并嘧啶结构域 (PYD),NLRPs 是模式识别受体,它们在先天免疫和细胞凋亡中发挥着重要作用,这一点得到了广泛的认可。然而,有几个 NLRP 因其作为在生殖和胚胎发育中具有重要作用的母源性基因的新的、特殊作用而受到关注。已经发现几个 NLRP 专门在卵母细胞和着床前胚胎中表达。有趣的是,与不同的功能一致,NLRP 基因显示出复杂的进化分歧。最明显的差异是人类特有的 NLRP7 基因,在啮齿动物中没有发现。然而,已经广泛使用小鼠模型来研究母源性 NLRP。NLRP2 和 NLRP5 蛋白是亚皮质母性复合物 (SCMC) 的组成部分,该复合物最近被确定对小鼠着床前发育至关重要。SCMC 整合了多种蛋白质,包括 KHDC3L、NLRP5、TLE6、OOEP、NLRP2 和 PADI6。NLRP5(也称为 MATER)已被广泛研究。在人类中,母亲体内特定 NLRP 基因的失活变异与后代的独特表型有关,例如双亲性葡萄胎 (BiHMs) 和早产。KHDC3L 和 NLRP5(和 NLRP7)的母源性隐性突变与生殖结局降低、BiHM 和广泛的多基因印记扰动有关。NLRPs 的精确机制尚不清楚,但研究强烈表明它们在基因组印记的建立和合子后甲基化维持等过程中发挥着关键作用。未来的挑战包括将小鼠模型的研究结果转化为人类背景,并将其应用于治疗和临床生育管理。

相似文献

1
The pivotal roles of the NOD-like receptors with a PYD domain, NLRPs, in oocytes and early embryo development†.含 PYDD 的 NOD 样受体(NLRPs)在卵母细胞和早期胚胎发育中的关键作用†。
Biol Reprod. 2019 Aug 1;101(2):284-296. doi: 10.1093/biolre/ioz098.
2
NLRPs, the subcortical maternal complex and genomic imprinting.NLRPs、皮质下母性复合物和基因组印记。
Reproduction. 2017 Dec;154(6):R161-R170. doi: 10.1530/REP-17-0465. Epub 2017 Sep 15.
3
NLRP7 participates in the human subcortical maternal complex and its variants cause female infertility characterized by early embryo arrest.NLRP7 参与人类皮质下母性复合物,其变体导致以早期胚胎停滞为特征的女性不孕。
J Mol Med (Berl). 2023 Jun;101(6):717-729. doi: 10.1007/s00109-023-02322-7. Epub 2023 May 6.
4
Variants in NLRP2 and ZFP36L2, non-core components of the human subcortical maternal complex, cause female infertility with embryonic development arrest.NLRP2 和 ZFP36L2 变异,人类皮质下母性复合物的非核心成分,导致胚胎发育阻滞的女性不孕。
Mol Hum Reprod. 2024 Sep 12;30(9). doi: 10.1093/molehr/gaae031.
5
Identification of oocyte-selective NLRP genes in rhesus macaque monkeys (Macaca mulatta).恒河猴(猕猴)中卵母细胞选择性NLRP基因的鉴定。
Mol Reprod Dev. 2009 Feb;76(2):151-9. doi: 10.1002/mrd.20937.
6
No evidence for mutations in NLRP7, NLRP2 or KHDC3L in women with unexplained recurrent pregnancy loss or infertility.在不明原因复发性流产或不孕女性中,未发现NLRP7、NLRP2或KHDC3L存在突变的证据。
Hum Reprod. 2015 Jan;30(1):232-8. doi: 10.1093/humrep/deu296. Epub 2014 Nov 5.
7
Expression analysis of the NLRP gene family suggests a role in human preimplantation development.NLRP基因家族的表达分析表明其在人类植入前发育中发挥作用。
PLoS One. 2008 Jul 23;3(7):e2755. doi: 10.1371/journal.pone.0002755.
8
Reproductive Outcomes from Maternal Loss of Nlrp2 Are Not Improved by IVF or Embryo Transfer Consistent with Oocyte-Specific Defect.母源 NLRP2 缺失导致的生殖结局无法通过 IVF 或胚胎移植得到改善,与卵母细胞特异性缺陷一致。
Reprod Sci. 2021 Jul;28(7):1850-1865. doi: 10.1007/s43032-020-00360-x. Epub 2020 Oct 22.
9
NLRP7 and KHDC3L, the two maternal-effect proteins responsible for recurrent hydatidiform moles, co-localize to the oocyte cytoskeleton.NLRP7和KHDC3L这两种导致复发性葡萄胎的母源效应蛋白共定位于卵母细胞细胞骨架。
Hum Reprod. 2015 Jan;30(1):159-69. doi: 10.1093/humrep/deu291. Epub 2014 Oct 29.
10
Novel pathogenic variants in NLRP7, NLRP5, and PADI6 in patients with recurrent hydatidiform moles and reproductive failure.在复发性葡萄胎和生殖失败患者中,NLRP7、NLRP5 和 PADI6 中的新型致病性变异体。
Clin Genet. 2021 Jun;99(6):823-828. doi: 10.1111/cge.13941. Epub 2021 Feb 23.

引用本文的文献

1
Piperine protects against cerebral ischemic injury by regulating the Caspase-1-mediated pyroptosis pathway.胡椒碱通过调节半胱天冬酶-1介导的细胞焦亡途径来预防脑缺血损伤。
Front Pharmacol. 2025 Jul 25;16:1601873. doi: 10.3389/fphar.2025.1601873. eCollection 2025.
2
A novel homozygous mutation in the NLRP2 gene causes early embryonic arrest.NLRP2基因中的一种新型纯合突变导致早期胚胎停滞。
J Assist Reprod Genet. 2024 Dec;41(12):3347-3355. doi: 10.1007/s10815-024-03279-3. Epub 2024 Nov 25.
3
Identification and exploration of pharmacological pyroptosis-related biomarkers of ulcerative colitis.
溃疡性结肠炎相关药物性 pyroptosis 生物学标志物的鉴定与探索。
Front Immunol. 2022 Oct 13;13:998470. doi: 10.3389/fimmu.2022.998470. eCollection 2022.
4
Genetic screening of Chinese patients with hydatidiform mole by whole-exome sequencing and comprehensive analysis.对中国葡萄胎患者进行全外显子组测序和综合分析的遗传筛查。
J Assist Reprod Genet. 2022 Oct;39(10):2403-2411. doi: 10.1007/s10815-022-02592-z. Epub 2022 Aug 24.
5
NOD2 and reproduction-associated NOD-like receptors have been lost during the evolution of pangolins.在穿山甲的进化过程中,NOD2及与生殖相关的NOD样受体已经消失。
Immunogenetics. 2022 Apr;74(2):261-268. doi: 10.1007/s00251-021-01230-9. Epub 2021 Nov 1.
6
Single-cell RNA sequencing reveals regulation of fetal ovary development in the monkey (Macaca fascicularis).单细胞RNA测序揭示了猕猴(食蟹猴)胎儿卵巢发育的调控机制。
Cell Discov. 2020 Dec 29;6(1):97. doi: 10.1038/s41421-020-00219-0.
7
Reproductive Outcomes from Maternal Loss of Nlrp2 Are Not Improved by IVF or Embryo Transfer Consistent with Oocyte-Specific Defect.母源 NLRP2 缺失导致的生殖结局无法通过 IVF 或胚胎移植得到改善,与卵母细胞特异性缺陷一致。
Reprod Sci. 2021 Jul;28(7):1850-1865. doi: 10.1007/s43032-020-00360-x. Epub 2020 Oct 22.
8
CRISPR/Cas9-Mediated Genome Editing Reveals Family Genes are Dispensable for Female Fertility in Mice.CRISPR/Cas9 介导的基因组编辑揭示家族基因对于小鼠的雌性生育力并非必需。
Cells. 2020 Mar 28;9(4):821. doi: 10.3390/cells9040821.
9
Listening to mother: Long-term maternal effects in mammalian development.倾听母亲:哺乳动物发育中的长期母体影响。
Mol Reprod Dev. 2020 Apr;87(4):399-408. doi: 10.1002/mrd.23336. Epub 2020 Mar 22.
10
Is Involved in the Differentiation of the Decidual Macrophages.参与蜕膜巨噬细胞的分化。
Int J Mol Sci. 2019 Nov 28;20(23):5994. doi: 10.3390/ijms20235994.