Internal Affairs: Tenascin-C as a Clinically Relevant, Endogenous Driver of Innate Immunity

63Citations
Citations of this article
64Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

To protect against danger, the innate immune system must promptly and accurately sense alarm signals, and mount an appropriate response to restore homeostasis. One endogenous trigger of immunity is tenascin-C, a large hexameric protein of the extracellular matrix. Upregulated upon tissue injury and cellular stress, tenascin-C is expressed during inflammation and tissue remodeling, where it influences cellular behavior by interacting with a multitude of molecular targets, including other matrix components, cell surface proteins, and growth factors. Here, we discuss how these interactions confer upon tenascin-C distinct immunomodulatory capabilities that make this matrix molecule necessary for efficient tissue repair. We also highlight in vivo studies that provide insight into the consequences of misregulated tenascin-C expression on inflammation and fibrosis during a wide range of inflammatory diseases. Finally, we examine how its unique expression pattern and inflammatory actions make tenascin-C a viable target for clinical exploitation in both diagnostic and therapeutic arenas.

Cite

CITATION STYLE

APA

Marzeda, A. M., & Midwood, K. S. (2018, April 1). Internal Affairs: Tenascin-C as a Clinically Relevant, Endogenous Driver of Innate Immunity. Journal of Histochemistry and Cytochemistry. SAGE Publications Ltd. https://doi.org/10.1369/0022155418757443

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free