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无脊椎动物的母胎营养与胎盘形成:一种新范式。

Matrotrophy and placentation in invertebrates: a new paradigm.

作者信息

Ostrovsky Andrew N, Lidgard Scott, Gordon Dennis P, Schwaha Thomas, Genikhovich Grigory, Ereskovsky Alexander V

机构信息

Department of Invertebrate Zoology, Faculty of Biology, Saint Petersburg State University, Universitetskaja nab. 7/9, 199034, Saint Petersburg, Russia.

Department of Palaeontology, Faculty of Earth Sciences, Geography and Astronomy, Geozentrum, University of Vienna, Althanstrasse 14, A-1090, Vienna, Austria.

出版信息

Biol Rev Camb Philos Soc. 2016 Aug;91(3):673-711. doi: 10.1111/brv.12189. Epub 2015 Apr 29.

DOI:10.1111/brv.12189
PMID:25925633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5098176/
Abstract

Matrotrophy, the continuous extra-vitelline supply of nutrients from the parent to the progeny during gestation, is one of the masterpieces of nature, contributing to offspring fitness and often correlated with evolutionary diversification. The most elaborate form of matrotrophy-placentotrophy-is well known for its broad occurrence among vertebrates, but the comparative distribution and structural diversity of matrotrophic expression among invertebrates is wanting. In the first comprehensive analysis of matrotrophy across the animal kingdom, we report that regardless of the degree of expression, it is established or inferred in at least 21 of 34 animal phyla, significantly exceeding previous accounts and changing the old paradigm that these phenomena are infrequent among invertebrates. In 10 phyla, matrotrophy is represented by only one or a few species, whereas in 11 it is either not uncommon or widespread and even pervasive. Among invertebrate phyla, Platyhelminthes, Arthropoda and Bryozoa dominate, with 162, 83 and 53 partly or wholly matrotrophic families, respectively. In comparison, Chordata has more than 220 families that include or consist entirely of matrotrophic species. We analysed the distribution of reproductive patterns among and within invertebrate phyla using recently published molecular phylogenies: matrotrophy has seemingly evolved at least 140 times in all major superclades: Parazoa and Eumetazoa, Radiata and Bilateria, Protostomia and Deuterostomia, Lophotrochozoa and Ecdysozoa. In Cycliophora and some Digenea, it may have evolved twice in the same life cycle. The provisioning of developing young is associated with almost all known types of incubation chambers, with matrotrophic viviparity more widespread (20 phyla) than brooding (10 phyla). In nine phyla, both matrotrophic incubation types are present. Matrotrophy is expressed in five nutritive modes, of which histotrophy and placentotrophy are most prevalent. Oophagy, embryophagy and histophagy are rarer, plausibly evolving through heterochronous development of the embryonic mouthparts and digestive system. During gestation, matrotrophic modes can shift, intergrade, and be performed simultaneously. Invertebrate matrotrophic adaptations are less complex structurally than in chordates, but they are more diverse, being formed either by a parent, embryo, or both. In a broad and still preliminary sense, there are indications of trends or grades of evolutionarily increasing complexity of nutritive structures: formation of (i) local zones of enhanced nutritional transport (placental analogues), including specialized parent-offspring cell complexes and various appendages increasing the entire secreting and absorbing surfaces as well as the contact surface between embryo and parent, (ii) compartmentalization of the common incubatory space into more compact and 'isolated' chambers with presumably more effective nutritional relationships, and (iii) internal secretory ('milk') glands. Some placental analogues in onychophorans and arthropods mimic the simplest placental variants in vertebrates, comprising striking examples of convergent evolution acting at all levels-positional, structural and physiological.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f97f/5098176/17dcee351a11/BRV-91-673-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f97f/5098176/17dcee351a11/BRV-91-673-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f97f/5098176/17dcee351a11/BRV-91-673-g001.jpg
摘要

母体营养供应,即在妊娠期从母体向子代持续提供卵黄外营养物质,是大自然的杰作之一,有助于子代健康,且常常与进化多样化相关。母体营养供应最复杂的形式——胎盘营养——因其在脊椎动物中广泛存在而为人熟知,但无脊椎动物中母体营养表达的比较分布和结构多样性尚不清楚。在对整个动物界母体营养供应的首次全面分析中,我们报告称,无论表达程度如何,在34个动物门中的至少21个门中已确定或推断存在母体营养供应,这显著超过了以往的记录,并改变了这些现象在无脊椎动物中不常见的旧有观念。在10个门中,母体营养供应仅由一个或少数几个物种代表,而在11个门中,它并非不常见或广泛存在,甚至普遍存在。在无脊椎动物门中,扁形动物门、节肢动物门和苔藓虫门占主导地位,分别有162、83和53个部分或完全具有母体营养的科。相比之下,脊索动物门有超过220个科包含或完全由具有母体营养的物种组成。我们利用最近发表的分子系统发育树分析了无脊椎动物门之间和门内生殖模式的分布:母体营养供应似乎在所有主要超类群中至少进化了140次:侧生动物和真后生动物、辐射对称动物和两侧对称动物、原口动物和后口动物、冠轮动物和蜕皮动物。在环口动物和一些复殖吸虫中,它可能在同一生命周期中进化了两次。为发育中的幼体提供营养与几乎所有已知类型的孵化室相关,母体营养胎生比育雏更为广泛(20个门)(育雏为10个门)。在9个门中,两种母体营养孵化类型都存在。母体营养供应以五种营养模式表达,其中组织营养和胎盘营养最为普遍。卵食、胚胎食和组织食较为罕见,可以推测是通过胚胎口器和消化系统的异时发育进化而来。在妊娠期,母体营养模式可以转变、过渡并同时进行。无脊椎动物的母体营养适应在结构上比脊索动物简单,但更为多样,由母体、胚胎或两者形成。从广泛且仍属初步的意义上讲,有迹象表明营养结构在进化上有日益复杂的趋势或等级:(i)形成增强营养运输的局部区域(类似胎盘),包括专门的亲代 - 子代细胞复合体以及各种增加整个分泌和吸收表面以及胚胎与母体之间接触表面的附属物,(ii)将共同的孵化空间分隔成更紧凑和“隔离”的腔室,可能具有更有效的营养关系,以及(iii)内部分泌(“乳汁”)腺。有爪动物和节肢动物中的一些类似胎盘的结构模仿了脊椎动物中最简单的胎盘变体,构成了在位置、结构和生理等所有层面上趋同进化的显著例子。

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本文引用的文献

1
The cell lineages of two types of embryo and a hermaphroditic gonad in dicyemid mesozoans.双胚虫中生动物的两种胚胎和雌雄同体性腺的细胞谱系。
Dev Growth Differ. 1996 Oct;38(5):453-463. doi: 10.1046/j.1440-169X.1996.t01-4-00002.x.
2
Context of diversification of the viviparous Gyrodactylidae (Platyhelminthes, Monogenoidea).胎生三代虫科(扁形动物门,单殖亚纲)的多样化背景。
Zool Scr. 2003 Sep;32(5):437-448. doi: 10.1046/j.1463-6409.2003.00130.x. Epub 2003 Aug 13.
3
A simplified placenta-like system for the transport of extraembryonic nutrients during embryogenesis of Bugula neritina (bryozoa).
在太平洋拟步甲蟑螂中,日常活动节律、睡眠和怀孕有着根本的关联。
bioRxiv. 2025 Mar 6:2025.02.27.640076. doi: 10.1101/2025.02.27.640076.
4
Gallophilous theory of cyclical parthenogenesis in aphids (Homoptera, Aphidinea).蚜虫(同翅目,蚜亚目)周期性孤雌生殖的嗜瘿理论。
Comp Cytogenet. 2024 Dec 17;18:247-276. doi: 10.3897/compcytogen.18.136095. eCollection 2024.
5
Natural variation in the egg-laying circuit modulates an intergenerational fitness trade-off.产卵回路的自然变异调节了代际间的适应度权衡。
Elife. 2024 Apr 2;12:RP88253. doi: 10.7554/eLife.88253.
6
Multiple evolutionary transitions of reproductive strategies in a phylum of aquatic colonial invertebrates.多细胞水生群体无脊椎动物门中生殖策略的多次进化转变。
Proc Biol Sci. 2023 Nov 8;290(2010):20231458. doi: 10.1098/rspb.2023.1458. Epub 2023 Nov 1.
7
Live-bearing cockroach genome reveals convergent evolutionary mechanisms linked to viviparity in insects and beyond.胎生蟑螂基因组揭示了与昆虫及其他生物胎生相关的趋同进化机制。
iScience. 2023 Sep 9;26(10):107832. doi: 10.1016/j.isci.2023.107832. eCollection 2023 Oct 20.
8
Genetic evidence for plastic reproductive philopatry and matrotrophy in blacktip reef sharks (Carcharhinus melanopterus) of the Moorea Island (French Polynesia).遗传证据表明,莫雷阿岛(法属波利尼西亚)的黑鳍礁鲨(Carcharhinus melanopterus)具有可塑性的生殖回游和母源营养。
Sci Rep. 2023 Sep 9;13(1):14913. doi: 10.1038/s41598-023-40140-6.
9
The developmental and structural uniqueness of the embryo of the extremophile viviparous nematode, .嗜极胎生线虫胚胎的发育和结构独特性,
Front Physiol. 2023 Jun 22;14:1197477. doi: 10.3389/fphys.2023.1197477. eCollection 2023.
10
Tsetse flies () choose birthing sites guided by substrate cues with no evidence for a role of pheromones.采采蝇()选择产仔地是由基质线索引导的,没有证据表明信息素起作用。
Proc Biol Sci. 2023 Apr 26;290(1997):20230030. doi: 10.1098/rspb.2023.0030.
一种用于在苔藓虫类的内肛苔藓虫胚胎发育过程中运输胚外营养物质的简化胎盘样系统。
J Morphol. 1975 Nov;147(3):355-377. doi: 10.1002/jmor.1051470308.
4
The role of the follicular epithelium in growing eggs of a dipteran insect during late oogenesis and cleavage.卵泡上皮在双翅目昆虫卵后期卵子发生和卵裂过程中对生长中卵子的作用。
J Morphol. 1983 Dec;178(3):303-312. doi: 10.1002/jmor.1051780307.
5
Morphology, ultrastructure, and germ cell cluster formation in ovarioles of aphids.蚜虫卵巢小管的形态学、超微结构及生殖细胞簇形成
J Morphol. 1985 Nov;186(2):209-221. doi: 10.1002/jmor.1051860206.
6
Viviparous development in Botrylloides (Compound Ascidians).菊海鞘(复合海鞘)的胎生发育
J Morphol. 1987 Sep;193(3):263-276. doi: 10.1002/jmor.1051930305.
7
Some aspects of segment formation and post-placental development in Peripatus acacioi marcus and marcus (Onychophora).马氏栉蚕(有爪动物门)中体节形成和胎盘后发育的某些方面。
J Morphol. 1988 Feb;195(2):123-140. doi: 10.1002/jmor.1051950202.
8
Structural characteristics of marsupial brood pouches of the antarctic sea urchins Abatus nimrodi and Abatus shackletoni (Echinoidea: Spatangoida).南极海胆尼氏阿巴海胆和沙氏阿巴海胆(棘皮动物门:心形海胆纲)有袋育儿袋的结构特征
J Morphol. 1993 Apr;216(1):79-93. doi: 10.1002/jmor.1052160109.
9
Developing embryo and cyclic changes in the uterus of Peripatus (Macroperipatus) acacioi (Onychophora, Peripatidae).阿卡西奥氏栉蚕(有爪动物门,栉蚕科)发育中的胚胎与子宫的周期性变化
J Morphol. 1995 May;224(2):179-198. doi: 10.1002/jmor.1052240207.
10
Matrotrophic adaptations and early stages of embryogenesis in the desert scorpion Paruroctonus mesaensis (Vaejovidae).沙漠蝎子梅萨副糙尾蝎(糙尾蝎科)的母体营养适应与胚胎发育早期阶段
J Morphol. 1998 Sep;237(3):187-211. doi: 10.1002/(SICI)1097-4687(199809)237:3<187::AID-JMOR1>3.0.CO;2-X.