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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Published in: | Frontiers in immunology Vol. 8; p. 1908 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Switzerland
Frontiers Media S.A
05-01-2018
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Subjects: | |
Online Access: | Get full text |
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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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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 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 |