Maternal recognition of pregnancy in the pig: A servomechanism involving sex steroids, cytokines and prostaglandins

IF 2.2 2区 农林科学 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE Animal Reproduction Science Pub Date : 2024-03-12 DOI:10.1016/j.anireprosci.2024.107452
Rodney D. Geisert , Fuller W. Bazer , Caroline G. Lucas , Caroline A. Pfeiffer , Ashley E. Meyer , Riley Sullivan , Destiny N. Johns , Mariana Sponchiado , Randall S. Prather
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Abstract

Maternal recognition of pregnancy (MRP) is a term utilized in mammals to describe pathways in which the conceptus alters the endometrial environment to prevent regression of corpora lutea to ensure continued production of progesterone (P4) required for establishment and maintenance of pregnancy. For nearly 40 years after publication of the endocrine/exocrine theory, conceptus estrogen (E2) was considered the primary maternal recognition signal in the pig. Conceptus production of prostaglandin E2 (PGE2) was also considered to be a major factor in preventing luteolysis. An addition to E2 and PGE2, pig conceptuses produce interleukin 1B2 (IL1B2) and interferons (IFN) delta (IFND) and gamma (IFNG). The present review provides brief history of the discovery of E2, PGs and IFNS which led to research investigating the role of these conceptus secreted factors in establishing and maintaining pregnancy in the pig. The recent utilization of gene editing technology allowed a more direct approach to investigate the in vivo roles of IL1B2, E2, PGE2, AND IFNG for establishment of pregnancy. These studies revealed unknown functions for IFNG and ILB2 in addition to PGE2 and E2. Thus, pregnancy recognition signal is via a servomechanism in requiring sequential effects of P4, E2, IL1B2, PGE2 and IFNG. Results indicate that the original established dogma for the role of conceptus E2 and PGs in MRP is a far too simplified model that involves the interplay of numerous mechanisms for inhibiting luteolysis, inducing critical elongation of the conceptuses and resolution of inflammation in pigs.

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猪母体对怀孕的识别:涉及性类固醇、细胞因子和前列腺素的服务机制
母体识别妊娠(MRP)是哺乳动物的一个术语,用于描述受体改变子宫内膜环境以防止黄体退化,从而确保持续产生建立和维持妊娠所需的孕酮(P4)的途径。在内分泌/外分泌理论发表后的近 40 年中,受体雌激素(E2)一直被认为是猪的主要母体识别信号。受体产生的前列腺素 E2(PGE2)也被认为是防止黄体溶解的主要因素。除 E2 和 PGE2 外,猪的受体还能产生白细胞介素 1B2 (IL1B2) 和干扰素 (IFN) δ (IFND) 及 γ (IFNG)。本综述简要介绍了发现 E2、PGs 和 IFNS 的历史,这些发现促使人们开始研究这些受体分泌因子在建立和维持猪妊娠中的作用。最近,基因编辑技术的使用使得研究 IL1B2、E2、PGE2 和 IFNG 在建立妊娠中的作用有了更直接的方法。这些研究揭示了除 PGE2 和 E2 外,IFNG 和 ILB2 的未知功能。因此,妊娠识别信号是通过一种伺服机制,需要 P4、E2、IL1B2、PGE2 和 IFNG 的相继作用。研究结果表明,最初关于受体 E2 和 PGs 在 MRP 中的作用的教条是一个过于简化的模型,它涉及到抑制黄体溶解、诱导受体临界伸长和解决猪的炎症等多种机制的相互作用。
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来源期刊
Animal Reproduction Science
Animal Reproduction Science 农林科学-奶制品与动物科学
CiteScore
4.50
自引率
9.10%
发文量
136
审稿时长
54 days
期刊介绍: Animal Reproduction Science publishes results from studies relating to reproduction and fertility in animals. This includes both fundamental research and applied studies, including management practices that increase our understanding of the biology and manipulation of reproduction. Manuscripts should go into depth in the mechanisms involved in the research reported, rather than a give a mere description of findings. The focus is on animals that are useful to humans including food- and fibre-producing; companion/recreational; captive; and endangered species including zoo animals, but excluding laboratory animals unless the results of the study provide new information that impacts the basic understanding of the biology or manipulation of reproduction. The journal''s scope includes the study of reproductive physiology and endocrinology, reproductive cycles, natural and artificial control of reproduction, preservation and use of gametes and embryos, pregnancy and parturition, infertility and sterility, diagnostic and therapeutic techniques. The Editorial Board of Animal Reproduction Science has decided not to publish papers in which there is an exclusive examination of the in vitro development of oocytes and embryos; however, there will be consideration of papers that include in vitro studies where the source of the oocytes and/or development of the embryos beyond the blastocyst stage is part of the experimental design.
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