C. elegans epicuticlins define specific compartments in the apical extracellular matrix and function in wound repair.

IF 3.7 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY Development Pub Date : 2024-11-01 Epub Date: 2024-10-23 DOI:10.1242/dev.204330
Murugesan Pooranachithra, Erin M Jyo, Nicolas Brouilly, Nathalie Pujol, Andreas M Ernst, Andrew D Chisholm
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Abstract

The apical extracellular matrix (aECM) of external epithelia often contains lipid-rich outer layers that contribute to permeability barrier function. The external aECM of nematodes is known as the cuticle and contains an external lipid-rich layer - the epicuticle. Epicuticlins are a family of tandem repeat cuticle proteins of unknown function. Here, we analyze the localization and function of the three C. elegans epicuticlins (EPIC proteins). EPIC-1 and EPIC-2 localize to the surface of the cuticle near the outer lipid layer, as well as to interfacial cuticles and adult-specific struts. EPIC-3 is expressed in dauer larvae and localizes to interfacial aECM in the buccal cavity. Skin wounding in the adult induces epic-3 expression, and EPIC proteins localize to wound sites. Null mutants lacking EPIC proteins are viable with reduced permeability barrier function and normal epicuticle lipid mobility. Loss of function in EPIC genes modifies the skin blistering phenotypes of Bli mutants and reduces survival after skin wounding. Our results suggest EPIC proteins define specific cortical compartments of the aECM and promote wound repair.

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秀丽隐杆线虫的表皮鞘氨醇确定了细胞外基质顶端的特定区域,并在伤口修复中发挥作用。
外部上皮细胞的顶端细胞外基质(aECM)通常含有富含脂质的外层,有助于发挥渗透屏障功能。线虫的外部细胞外基质被称为角质层,包含一个富含脂质的外层,即表皮层。Epicuticlins是一个串联重复的角质层蛋白家族,其功能未知。在这里,我们分析了三种秀丽隐杆线虫表角质层蛋白(EPIC蛋白)的定位和功能。EPIC-1和EPIC-2定位于外脂层附近的角质层表面,以及界面角质层和成虫特异性支柱。EPIC-3表达于足幼虫,定位于颊腔的界面角质层。成虫的皮肤伤口会诱导 EPIC-3 的表达,EPIC 蛋白会定位到伤口部位。缺乏EPIC蛋白的缺失突变体可以存活,但渗透屏障功能降低,表皮脂质流动性正常。史诗基因功能缺失会改变bli突变体的皮肤水疱表型,并降低皮肤受伤后的存活率。我们的研究结果表明,EPIC 蛋白定义了 aECM 的特定皮质区,并促进了伤口修复。
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来源期刊
Development
Development 生物-发育生物学
CiteScore
6.70
自引率
4.30%
发文量
433
审稿时长
3 months
期刊介绍: Development’s scope covers all aspects of plant and animal development, including stem cell biology and regeneration. The single most important criterion for acceptance in Development is scientific excellence. Research papers (articles and reports) should therefore pose and test a significant hypothesis or address a significant question, and should provide novel perspectives that advance our understanding of development. We also encourage submission of papers that use computational methods or mathematical models to obtain significant new insights into developmental biology topics. Manuscripts that are descriptive in nature will be considered only when they lay important groundwork for a field and/or provide novel resources for understanding developmental processes of broad interest to the community. Development includes a Techniques and Resources section for the publication of new methods, datasets, and other types of resources. Papers describing new techniques should include a proof-of-principle demonstration that the technique is valuable to the developmental biology community; they need not include in-depth follow-up analysis. The technique must be described in sufficient detail to be easily replicated by other investigators. Development will also consider protocol-type papers of exceptional interest to the community. We welcome submission of Resource papers, for example those reporting new databases, systems-level datasets, or genetic resources of major value to the developmental biology community. For all papers, the data or resource described must be made available to the community with minimal restrictions upon publication. To aid navigability, Development has dedicated sections of the journal to stem cells & regeneration and to human development. The criteria for acceptance into these sections is identical to those outlined above. Authors and editors are encouraged to nominate appropriate manuscripts for inclusion in one of these sections.
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