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一氧化氮在调控动物浮游底栖生活史中的古老作用:来自海洋海绵的证据。

An ancient role for nitric oxide in regulating the animal pelagobenthic life cycle: evidence from a marine sponge.

机构信息

School of Biological Sciences, University of Queensland, Brisbane QLD 4072, Australia.

Department of Physiology &Biophysics, Dalhousie University, Halifax NS B3H 4R2, Canada.

出版信息

Sci Rep. 2016 Nov 22;6:37546. doi: 10.1038/srep37546.

Abstract

In many marine invertebrates, larval metamorphosis is induced by environmental cues that activate sensory receptors and signalling pathways. Nitric oxide (NO) is a gaseous signalling molecule that regulates metamorphosis in diverse bilaterians. In most cases NO inhibits or represses this process, although it functions as an activator in some species. Here we demonstrate that NO positively regulates metamorphosis in the poriferan Amphimedon queenslandica. High rates of A. queenslandica metamorphosis normally induced by a coralline alga are inhibited by an inhibitor of nitric oxide synthase (NOS) and by a NO scavenger. Consistent with this, an artificial donor of NO induces metamorphosis even in the absence of the alga. Inhibition of the ERK signalling pathway prevents metamorphosis in concert with, or downstream of, NO signalling; a NO donor cannot override the ERK inhibitor. NOS gene expression is activated late in embryogenesis and in larvae, and is enriched in specific epithelial and subepithelial cell types, including a putative sensory cell, the globular cell; DAF-FM staining supports these cells being primary sources of NO. Together, these results are consistent with NO playing an activating role in induction of A. queenslandica metamorphosis, evidence of its highly conserved regulatory role in metamorphosis throughout the Metazoa.

摘要

在许多海洋无脊椎动物中,幼虫变态是由激活感觉受体和信号通路的环境线索诱导的。一氧化氮(NO)是一种气态信号分子,可调节各种两侧对称动物的变态。在大多数情况下,NO 抑制或抑制该过程,尽管在某些物种中它作为激活剂起作用。在这里,我们证明了 NO 可正调控多孔动物门 Amphimedon queenslandica 的变态。珊瑚藻通常会诱导 A. queenslandica 变态,但高浓度的 A. queenslandica 变态会被一氧化氮合酶(NOS)抑制剂和 NO 清除剂抑制。与此一致的是,即使没有藻类,NO 的人工供体也会诱导变态。ERK 信号通路的抑制与 NO 信号协同或下游阻止变态;NO 供体不能覆盖 ERK 抑制剂。NOS 基因表达在胚胎发生后期和幼虫中被激活,并在特定的上皮和上皮下细胞类型中富集,包括一种假定的感觉细胞,即球状细胞;DAF-FM 染色支持这些细胞是 NO 的主要来源。这些结果共同表明,NO 在诱导 A. queenslandica 变态中起激活作用,证明了其在整个后生动物中对变态的高度保守调节作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c90/5118744/f02f2910c68f/srep37546-f1.jpg

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