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Cited by 494

The DOI matches its Crossref record; 28 of the 28 references it cites were found in a registry or an index.

Mechanotransduction: All Signals Point to Cytoskeleton, Matrix, and Integrins

Alenghat, Francis J., Ingber, Donald E.·2002·Science's STKE

Abstract

Mechanical stresses modulate cell function by either activating or tuning signal transduction pathways. Mechanotransduction, the process by which cells convert mechanical stimuli into a chemical response, occurs both in cells specialized for sensing mechanical cues and in parenchymal cells whose primary function is not mechanosensory. However, common among the various responses to mechanical stress is the importance of direct or indirect connections between the internal cytoskeleton, the extracellular matrix (ECM), and traditional signal transducing molecules. In many instances, these elements converge at focal adhesions, sites of structural attachment between the cytoskeleton and ECM that are anchored by cell surface integrin receptors. Alenghat and Ingber discuss the accumulating evidence for the central role of cytoskeleton, ECM, and integrin-anchored focal adhesions in several mechanotransduction pathways.

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Metadata

Authors
Alenghat, F. J., & Ingber, D. E.
Venue
Science's STKE
Published
2002-02-12
Volume
2002
Issue
119
Pages
pe6-pe6
ISSN
1525-8882 (ISSN-L)
OpenAlex
W2153287457
Cited by
494
References
28
FWCI
7.08
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Mechanotransduction: All Signals Point to Cytoskeleton, Matrix, and Integrins. https://app.cochat.ai/papers/10.1126/stke.2002.119.pe6
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Alenghat, F. J., & Ingber, D. E. (2002). Mechanotransduction: All Signals Point to Cytoskeleton, Matrix, and Integrins. Science's STKE. https://doi.org/10.1126/stke.2002.119.pe6

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.