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流星素调节左右组织者的形成以及脊椎动物身体不对称性的建立。

Meteorins regulate the formation of the left-right organizer and the establishment of vertebrate body asymmetry.

作者信息

Eggeler Fanny, Boulanger-Weill Jonathan, De Santis Flavia, Belleri Laura, Duroure Karine, Auer Thomas O, Albadri Shahad, Del Bene Filippo

机构信息

Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.

Institut Curie, PSL Research University, Paris, France.

出版信息

Elife. 2025 Aug 1;14:RP105430. doi: 10.7554/eLife.105430.

Abstract

While the exterior of vertebrate bodies appears bilaterally symmetrical, internal organ positioning and morphology frequently exhibit left-right (L-R) asymmetries. In several vertebrates, including human, mouse, frog, and zebrafish, left-right symmetry-breaking during embryonic development is initiated by a ciliated organ called the Node or left-right organizer. Within the Node, a leftward flow of extraembryonic fluid named the Nodal flow mediates the asymmetric expressions of Nodal factors. Although downstream Nodal pathway components leading to the establishment of the embryonic left-right axis are well known, less is known about the development and formation of the embryonic Node itself. Here, we reveal a novel role for the Meteorin protein family in the establishment of the left-right axis and in the formation of Kupffer's vesicle, the Node equivalent structure in zebrafish. We show that the genetic inactivation of each or all three members of the zebrafish Meteorin family (, and ) leads to defects in properties of the Kupffer's vesicle, caused by impaired assembly and migration of the Kupffer's vesicle forming dorsal forerunner cells. In addition, we demonstrate that Meteorins genetically interact with integrins ItgαV and Itgβ1b, regulating the dorsal forerunner cell clustering, and that loss-of-function results in disturbed Nodal factor expression and consequently in randomized or symmetric heart looping and jogging. These results identify a new role for the Meteorin protein family in the left-right asymmetry patterning during embryonic vertebrate development.

摘要

虽然脊椎动物身体的外部看起来是左右对称的,但内部器官的定位和形态常常表现出左右(L-R)不对称性。在包括人类、小鼠、青蛙和斑马鱼在内的几种脊椎动物中,胚胎发育过程中的左右对称性打破是由一个名为节点或左右组织者的纤毛器官启动的。在节点内,一种名为节点流的胚外液向左流动介导了节点因子的不对称表达。虽然导致胚胎左右轴建立的下游节点通路成分是众所周知的,但关于胚胎节点本身的发育和形成却知之甚少。在这里,我们揭示了流星蛋白家族在左右轴建立和斑马鱼中与节点等效结构库普弗囊泡形成中的新作用。我们表明,斑马鱼流星蛋白家族的每个成员或所有三个成员(、和)的基因失活会导致库普弗囊泡特性的缺陷,这是由形成库普弗囊泡的背侧先驱细胞的组装和迁移受损引起的。此外,我们证明流星蛋白与整合素ItgαV和Itgβ1b发生遗传相互作用,调节背侧先驱细胞的聚集,并且功能丧失会导致节点因子表达紊乱,从而导致心脏环化和跳动随机化或对称化。这些结果确定了流星蛋白家族在胚胎脊椎动物发育过程中左右不对称模式形成中的新作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b123/12316458/74cf24d9c54e/elife-105430-fig1.jpg

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