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An ECM-to-Nucleus Signaling Pathway Activates Lysosomes for C. elegans Larval Development.

Rui Miao | Meijiao Li | Qianqian Zhang | Chonglin Yang | Xiaochen Wang
Developmental cell | 2020

Lysosomes degrade macromolecular cargos, recycle catabolites, and serve as signaling platforms to maintain cell homeostasis, but their role at the tissue level is unclear. Here, we investigate lysosome regulation and function during C. elegans molting, a specialized extracellular matrix (ECM) remodeling process essential for larval development. We found that lysosomes are specifically activated in the epidermis at molt when the apical ECM (cuticle) is being replaced. Impaired lysosome function affects endocytic cargo degradation, suppresses elevated protein synthesis at molt, and causes molting defects. Disturbance of ECM-epidermis attachments triggers lysosomal activation and induces expression of the vacuolar H+-ATPase (V-ATPase), which is mediated by the GATA transcription factor ELT-3 and the STAT family protein STA-2. Our study reveals an ECM-to-nucleus signaling pathway that activates lysosomes to facilitate ECM remodeling essential for larval development.

Pubmed ID: 31735670

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This is a list of tools and resources that we have found mentioned in this publication.


N2_(ancestral) (tool)

RRID:WB-STRAIN:WBStrain00000003

Caenorhabditis elegans with name C. elegans wild type (ancestral). from WB.

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intermediate filament subunit antibody - Waterston, R.H.; (antibody)

RRID:AB_528312

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Mouse Anti-Caenorhabditis elegans myotactin Monoclonal Antibody, Unconjugated (antibody)

RRID:AB_528387

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Anti-Puromycin Antibody, clone 12D10 (antibody)

RRID:AB_2566826

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