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敲低CXCL14会破坏眼部发育过程中的神经血管模式。

Knockdown of CXCL14 disrupts neurovascular patterning during ocular development.

作者信息

Ojeda Ana F, Munjaal Ravi P, Lwigale Peter Y

机构信息

BioSciences, Rice University, 6100 Main Street, Houston, TX, United States; Universidad Santo Tomas, sede Puerto Montt, Buenavecindad #91, Décima región de los Lagos, Chile.

BioSciences, Rice University, 6100 Main Street, Houston, TX, United States.

出版信息

Dev Biol. 2017 Mar 1;423(1):77-91. doi: 10.1016/j.ydbio.2017.01.008. Epub 2017 Jan 15.

Abstract

The C-X-C motif ligand 14 (CXCL14) is a recently discovered chemokine that is highly conserved in vertebrates and expressed in various embryonic and adult tissues. CXCL14 signaling has been implicated to function as an antiangiogenic and anticancer agent in adults. However, its function during development is unknown. We previously identified novel expression of CXCL14 mRNA in various ocular tissues during development. Here, we show that CXCL14 protein is expressed in the anterior eye at a critical time during neurovascular development and in the retina during neurogenesis. We report that RCAS-mediated knockdown of CXCL14 causes severe neural defects in the eye including precocious and excessive innervation of the cornea and iris. Absence of CXCL14 results in the malformation of the neural retina and misprojection of the retinal ganglion neurons. The ocular neural defects may be due to loss of CXCL12 modulation since recombinant CXCL14 diminishes CXCL12-induced axon growth in vitro. Furthermore, we show that knockdown of CXCL14 causes neovascularization of the cornea. Altogether, our results show for the first time that CXCL14 plays a critical role in modulating neurogenesis and inhibiting ectopic vascularization of the cornea during ocular development.

摘要

C-X-C基序配体14(CXCL14)是一种最近发现的趋化因子,在脊椎动物中高度保守,并在各种胚胎和成年组织中表达。CXCL14信号传导在成体中被认为具有抗血管生成和抗癌作用。然而,其在发育过程中的功能尚不清楚。我们之前在发育过程中鉴定出CXCL14 mRNA在各种眼组织中的新表达。在此,我们表明CXCL14蛋白在神经血管发育的关键时期在前眼中表达,在神经发生期间在视网膜中表达。我们报告说,RCAS介导的CXCL14敲低会导致眼睛出现严重的神经缺陷,包括角膜和虹膜的早熟和过度神经支配。CXCL14的缺失导致神经视网膜畸形和视网膜神经节神经元的错误投射。眼部神经缺陷可能是由于CXCL12调节的丧失,因为重组CXCL14在体外会减少CXCL12诱导的轴突生长。此外,我们表明CXCL14的敲低会导致角膜新生血管形成。总之,我们的结果首次表明CXCL14在眼部发育过程中对调节神经发生和抑制角膜异位血管形成起着关键作用。

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