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

Mahboobeh Amoushahi, Lone Sunde, Karin Lykke-Hartmann*

*Kontaktforfatter

Publikation: Bidrag til tidsskriftReview (oversigtsartikel)peer review

14 Citationer (Scopus)

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.

OriginalsprogEngelsk
TidsskriftBiology of Reproduction
Vol/bind101
Udgave nummer2
Sider (fra-til)284-296
Antal sider13
ISSN0006-3363
DOI
StatusUdgivet - 1 aug. 2019
Udgivet eksterntJa

Bibliografisk note

Funding Information:
This work was supported by the Aarhus University research Found (AUFF) (to LS and KLH), the Novo Nordisk Foundation (NNF16OC0022480), Augustinus Fonden and Fonden til Laegevidenskabens Fremme (to KLH).

Publisher Copyright:
© 2019 The Author(s) . Published by Oxford University Press on behalf of Society for the Study of Reproduction.

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