S100 Proteins As an Important Regulator of Macrophage Inflammation

The S100 proteins, a family of calcium-binding cytosolic proteins, have a broad range of intracellular and extracellular functions through regulating calcium balance, cell apoptosis, migration, proliferation, differentiation, energy metabolism, and inflammation. The intracellular functions of S100 p...

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Bibliographic Details
Published in:Frontiers in immunology Vol. 8; p. 1908
Main Authors: Xia, Chang, Braunstein, Zachary, Toomey, Amelia C, Zhong, Jixin, Rao, Xiaoquan
Format: Journal Article
Language:English
Published: Switzerland Frontiers Media S.A 05-01-2018
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Summary:The S100 proteins, a family of calcium-binding cytosolic proteins, have a broad range of intracellular and extracellular functions through regulating calcium balance, cell apoptosis, migration, proliferation, differentiation, energy metabolism, and inflammation. The intracellular functions of S100 proteins involve interaction with intracellular receptors, membrane protein recruitment/transportation, transcriptional regulation and integrating with enzymes or nucleic acids, and DNA repair. The S100 proteins could also be released from the cytoplasm, induced by tissue/cell damage and cellular stress. The extracellular S100 proteins, serving as a danger signal, are crucial in regulating immune homeostasis, post-traumatic injury, and inflammation. Extracellular S100 proteins are also considered biomarkers for some specific diseases. In this review, we will discuss the multi-functional roles of S100 proteins, especially their potential roles associated with cell migration, differentiation, tissue repair, and inflammation.
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Edited by: Leticia A. Carneiro, Universidade Federal do Rio de Janeiro, Brazil
Specialty section: This article was submitted to Molecular Innate Immunity, a section of the journal Frontiers in Immunology
Reviewed by: Charles E. McCall, Wake Forest Baptist Medical Center, United States; Penghua Yang, University of Maryland, Baltimore, United States
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2017.01908