Complement Component C1q: Historical Perspective of a Functionally Versatile, and Structurally Unusual, Serum Protein

Complement component C1q plays an important recognition role in adaptive, and innate, immunity through its ability to interact, via its six globular head regions, with both immunoglobulin and non-immunoglobulin activators of the complement system, and also in the clearance of cell debris, and by pla...

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Main Author: Kenneth B. M. Reid
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-04-01
Series:Frontiers in Immunology
Subjects:
C1q
Online Access:http://journal.frontiersin.org/article/10.3389/fimmu.2018.00764/full
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spelling doaj-82cf6ff1e73d4479b0dea445410ba5b72020-11-25T00:07:03ZengFrontiers Media S.A.Frontiers in Immunology1664-32242018-04-01910.3389/fimmu.2018.00764355171Complement Component C1q: Historical Perspective of a Functionally Versatile, and Structurally Unusual, Serum ProteinKenneth B. M. ReidComplement component C1q plays an important recognition role in adaptive, and innate, immunity through its ability to interact, via its six globular head regions, with both immunoglobulin and non-immunoglobulin activators of the complement system, and also in the clearance of cell debris, and by playing a role in regulation of cellular events by interacting with a wide range of cell surface molecules. The presence of collagen-like triple-helical structures within C1q appears crucial to the presentation, and multivalent binding, of the globular heads of C1q to targets, and also to its association with the proenzyme complex of C1r2–C1s2, to yield the C1 complex. The possible role that movement of these collagen-like structures may play in the activation of the C1 complex is a controversial area, with there still being no definitive answer as to how the first C1r proenzyme molecule becomes activated within the C1 complex, thus allowing it to activate proenzyme C1s, and initiate and the consequent cascade of events in the activation of the classical pathway of complement. The globular heads of C1q are similar to domains found within the tumor necrosis factor (TNF) superfamily of proteins, and have been shown to bind to a very wide range of ligands. In addition to its well-defined roles in infection and immunity, a variety of other functions associated with C1q include possible roles, in the development of problems in the central nervous system, which occur with aging, and perhaps in the regulation of tumor growth.http://journal.frontiersin.org/article/10.3389/fimmu.2018.00764/fullC1 activationC1qcollagen-like structureglobular headstumoraging
collection DOAJ
language English
format Article
sources DOAJ
author Kenneth B. M. Reid
spellingShingle Kenneth B. M. Reid
Complement Component C1q: Historical Perspective of a Functionally Versatile, and Structurally Unusual, Serum Protein
Frontiers in Immunology
C1 activation
C1q
collagen-like structure
globular heads
tumor
aging
author_facet Kenneth B. M. Reid
author_sort Kenneth B. M. Reid
title Complement Component C1q: Historical Perspective of a Functionally Versatile, and Structurally Unusual, Serum Protein
title_short Complement Component C1q: Historical Perspective of a Functionally Versatile, and Structurally Unusual, Serum Protein
title_full Complement Component C1q: Historical Perspective of a Functionally Versatile, and Structurally Unusual, Serum Protein
title_fullStr Complement Component C1q: Historical Perspective of a Functionally Versatile, and Structurally Unusual, Serum Protein
title_full_unstemmed Complement Component C1q: Historical Perspective of a Functionally Versatile, and Structurally Unusual, Serum Protein
title_sort complement component c1q: historical perspective of a functionally versatile, and structurally unusual, serum protein
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2018-04-01
description Complement component C1q plays an important recognition role in adaptive, and innate, immunity through its ability to interact, via its six globular head regions, with both immunoglobulin and non-immunoglobulin activators of the complement system, and also in the clearance of cell debris, and by playing a role in regulation of cellular events by interacting with a wide range of cell surface molecules. The presence of collagen-like triple-helical structures within C1q appears crucial to the presentation, and multivalent binding, of the globular heads of C1q to targets, and also to its association with the proenzyme complex of C1r2–C1s2, to yield the C1 complex. The possible role that movement of these collagen-like structures may play in the activation of the C1 complex is a controversial area, with there still being no definitive answer as to how the first C1r proenzyme molecule becomes activated within the C1 complex, thus allowing it to activate proenzyme C1s, and initiate and the consequent cascade of events in the activation of the classical pathway of complement. The globular heads of C1q are similar to domains found within the tumor necrosis factor (TNF) superfamily of proteins, and have been shown to bind to a very wide range of ligands. In addition to its well-defined roles in infection and immunity, a variety of other functions associated with C1q include possible roles, in the development of problems in the central nervous system, which occur with aging, and perhaps in the regulation of tumor growth.
topic C1 activation
C1q
collagen-like structure
globular heads
tumor
aging
url http://journal.frontiersin.org/article/10.3389/fimmu.2018.00764/full
work_keys_str_mv AT kennethbmreid complementcomponentc1qhistoricalperspectiveofafunctionallyversatileandstructurallyunusualserumprotein
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