层粘连蛋白定义的机械状态调节视网膜色素上皮吞噬。

IF 6.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Aleksandra N Kozyrina, Teodora Piskova, Francesca Semeraro, Iris C Doolaar, Taspia Prapty, Tamás Haraszti, Maxime Hubert, Reinhard Windoffer, Rudolf E Leube, Ana-Sunčana Smith, Jacopo Di Russo
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引用次数: 0

摘要

上皮细胞表现出很强的相互联系,这对组织力学特性至关重要。在内稳态中,这些特性被称为机械内稳态,依赖于细胞间张力和细胞外基质(ECM)粘附力之间的平衡。虽然与年龄相关的ECM重塑与视网膜外疾病有关,但其在机械稳态中的基本作用尚不清楚。在我们的研究中,我们量化了视网膜色素上皮(RPE)力学状态的变化,揭示了与基底膜层粘连蛋白及其整合素受体β1和β4梯度的相关性。这种关系与光感受器外段循环利用的区域吞噬需求有关。利用还原论方法,我们发现层粘连蛋白332和层粘连蛋白511同工型在低密度下对β1和β4整合素的结合有不同的影响。值得注意的是,层粘连蛋白511通过降低β4与β1整合素的接合比来增强RPE的收缩性,从而降低吞噬效率。我们的研究结果表明,ecm定义的RPE力学状态可以作为视觉功能的新参数。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Laminin-defined mechanical status modulates retinal pigment epithelium phagocytosis.

Epithelial cells exhibit strong interconnections that are crucial for tissue mechanical properties. In homeostasis, these properties, termed mechanical homeostasis, depend on the balance between intercellular tension and extracellular matrix (ECM) adhesion forces. While age-related ECM remodeling is linked to outer retinal disease, its fundamental role in mechanical homeostasis remains unclear. In our study, we quantified changes in the mechanical state of retinal pigment epithelium (RPE), revealing a correlation with gradients of basement membrane laminins and their integrin receptors, β1 and β4. This relationship is related to regional phagocytic demand for recycling photoreceptor outer segments. Using a reductionist approach, we found that laminin 332 and laminin 511 isoforms differentially influence engagement with β1 and β4 integrins at low densities. Notably, laminin 511 enhances RPE contractility by reducing the β4 to β1 integrin engagement ratio, which subsequently diminishes phagocytic efficiency. Our findings suggest that the ECM-defined mechanical status of RPE serves as a novel parameter for visual function.

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来源期刊
EMBO Reports
EMBO Reports 生物-生化与分子生物学
CiteScore
11.20
自引率
1.30%
发文量
267
审稿时长
1 months
期刊介绍: EMBO Reports is a scientific journal that specializes in publishing research articles in the fields of molecular biology, cell biology, and developmental biology. The journal is known for its commitment to publishing high-quality, impactful research that provides novel physiological and functional insights. These insights are expected to be supported by robust evidence, with independent lines of inquiry validating the findings. The journal's scope includes both long and short-format papers, catering to different types of research contributions. It values studies that: Communicate major findings: Articles that report significant discoveries or advancements in the understanding of biological processes at the molecular, cellular, and developmental levels. Confirm important findings: Research that validates or supports existing knowledge in the field, reinforcing the reliability of previous studies. Refute prominent claims: Studies that challenge or disprove widely accepted ideas or hypotheses in the biosciences, contributing to the correction and evolution of scientific understanding. Present null data: Papers that report negative results or findings that do not support a particular hypothesis, which are crucial for the scientific process as they help to refine or redirect research efforts. EMBO Reports is dedicated to maintaining high standards of scientific rigor and integrity, ensuring that the research it publishes contributes meaningfully to the advancement of knowledge in the life sciences. By covering a broad spectrum of topics and encouraging the publication of both positive and negative results, the journal plays a vital role in promoting a comprehensive and balanced view of scientific inquiry. 
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