TY - JOUR
T1 - Complement's hidden arsenal
T2 - New insights and novel functions inside the cell
AU - Liszewski, M. Kathryn
AU - Elvington, Michelle
AU - Kulkarni, Hrishikesh S.
AU - Atkinson, John P.
N1 - Funding Information:
Support was provided by the National Institutes of Health (R01 GM0099111 and R01 AI041592 to J.P.A.), the National Institutes of Health Training in the Immunobiology of Rheumatic Disease (2T32 AR007279, to M.E.) and the National Institutes of Health Training Grant in the Principles of Pulmonary Research (5T32 HL007317, to H.S.K.). Research reported in this publication is supported by the National Institute of Arthritis and Musculoskeletal and Skin Diseases, part of the National Institutes of Health, under Award Number P30AR048335 and the National Institutes of Health Grant for the Washington University Institute of Clinical and Translational Sciences (3UL1 TR000448).
Publisher Copyright:
© 2017 Elsevier Ltd
PY - 2017/4/1
Y1 - 2017/4/1
N2 - A key component of both innate and adaptive immunity, new understandings of the complement system are expanding its roles beyond that traditionally appreciated. Evidence is accumulating that complement has an intracellular arsenal of components that provide not only immune defense, but also assist in key interactions for host cell functions. Although early work has primarily centered on T cells, the intracellular complement system likely functions in many if not most cells of the body. Some of these functions may trace their origins to the primitive complement system that began as a primeval form of C3 likely tasked for protection from intracellular pathogen invasion. This later expanded to include extracellular defense as C3 became a secreted protein to patrol the vasculature. Other components were added to the growing system including regulators to protect host cells from the indiscriminate effects of this potent system. Contemporary cells may retain some of these vestigial remnants. We now know that a) C3 serves as a damage-associated molecular pattern (in particular by coating pathogens that translocate into cells), b) most cells store C3 and recycle C3(H2O) for immediate use, and c) C3 assists in cellular survival and metabolic reprogramming. Other components also are part of this hidden arsenal including C5, properdin, factors H and B, and complement receptors. Importantly, better definition of the intracellular complement system may translate into new target discovery to assist in creating the next generation of complement therapeutics.
AB - A key component of both innate and adaptive immunity, new understandings of the complement system are expanding its roles beyond that traditionally appreciated. Evidence is accumulating that complement has an intracellular arsenal of components that provide not only immune defense, but also assist in key interactions for host cell functions. Although early work has primarily centered on T cells, the intracellular complement system likely functions in many if not most cells of the body. Some of these functions may trace their origins to the primitive complement system that began as a primeval form of C3 likely tasked for protection from intracellular pathogen invasion. This later expanded to include extracellular defense as C3 became a secreted protein to patrol the vasculature. Other components were added to the growing system including regulators to protect host cells from the indiscriminate effects of this potent system. Contemporary cells may retain some of these vestigial remnants. We now know that a) C3 serves as a damage-associated molecular pattern (in particular by coating pathogens that translocate into cells), b) most cells store C3 and recycle C3(H2O) for immediate use, and c) C3 assists in cellular survival and metabolic reprogramming. Other components also are part of this hidden arsenal including C5, properdin, factors H and B, and complement receptors. Importantly, better definition of the intracellular complement system may translate into new target discovery to assist in creating the next generation of complement therapeutics.
KW - C3
KW - C3(HO)
KW - CD46
KW - Complement
KW - Factor H
KW - Inflammasome
KW - Intracellular complement system
KW - Properdin
KW - T cells
UR - http://www.scopus.com/inward/record.url?scp=85011966019&partnerID=8YFLogxK
U2 - 10.1016/j.molimm.2017.01.004
DO - 10.1016/j.molimm.2017.01.004
M3 - Review article
C2 - 28196665
AN - SCOPUS:85011966019
SN - 0161-5890
VL - 84
SP - 2
EP - 9
JO - Molecular Immunology
JF - Molecular Immunology
ER -