Large, recursive membrane platforms are associated to Trop-1, Trop-2 and protein kinase signaling for cell growth.

IF 3.1 3区 生物学 Q3 CELL BIOLOGY
Marco Trerotola, Valeria Relli, Romina Tripaldi, Pasquale Simeone, Emanuela Guerra, Andrea Sacchetti, Martina Ceci, Ludovica Pantalone, Paolo Ciufici, Antonino Moschella, Valeria R Caiolfa, Moreno Zamai, Saverio Alberti
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引用次数: 0

Abstract

The transmembrane glycoproteins Trop-1/EpCAM and Trop-2 independently trigger Ca2+ and kinase signals for cell growth and tumor progression. Our findings indicated that Trop-1 and Trop-2 tightly colocalize at macroscopic, ruffle-like protrusions (RLP), that elevate from the cell perimeter, and locally recur over hundreds of seconds. These previously unrecognized elevated membrane regions ≥20 µm-long, up to 1.5 µm high were revealed by Z-stack analysis and three-dimensional reconstruction of signal transducer-hosting plasma membrane regions. Trop-2 stimulates cell growth through a membrane super-complex that comprises CD9, PKCα, ion pumps and cytoskeletal components. Our findings indicated that the growth-driving Trop-2 super-complex assembles at RLP. RLP behaved as sites of clustering of signal transducers, of phosphorylation/activation of growth-driving kinases, as recruitment sites of PKCα and as origin of Ca2+ signaling waves, suggesting RLP to be novel signaling platforms in living cells. RLP were induced by growth factors and disappeared upon growth factor deprivation and β-actin depolymerization, candidating RLP to be functional platforms for high-dimensional signaling for cell growth. [Media: see text] [Media: see text] [Media: see text] [Media: see text] [Media: see text] [Media: see text] [Media: see text] [Media: see text] [Media: see text] [Media: see text] [Media: see text] [Media: see text].

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来源期刊
Molecular Biology of the Cell
Molecular Biology of the Cell 生物-细胞生物学
CiteScore
6.00
自引率
6.10%
发文量
402
审稿时长
2 months
期刊介绍: MBoC publishes research articles that present conceptual advances of broad interest and significance within all areas of cell, molecular, and developmental biology. We welcome manuscripts that describe advances with applications across topics including but not limited to: cell growth and division; nuclear and cytoskeletal processes; membrane trafficking and autophagy; organelle biology; quantitative cell biology; physical cell biology and mechanobiology; cell signaling; stem cell biology and development; cancer biology; cellular immunology and microbial pathogenesis; cellular neurobiology; prokaryotic cell biology; and cell biology of disease.
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