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PMID: 3259727 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Cachectin/TNF and IL-1 induced by glucose-modified proteins: role in normal tissue remodeling.

Science (New York, N.Y.) ·Vol. 240 ·No. 4858 ·1988-06-10 ·Pages 1546-8

Vlassara H, Brownlee M, Manogue KR, Dinarello CA, Pasagian A

Abstract

Proteins undergo a series of nonenzymatic reactions with glucose over time to form advanced glycosylation end products (AGEs). Macrophages have a receptor that recognizes the AGE moiety and mediates the uptake and degradation of AGE proteins. This removal process is associated with the production and secretion of cachectin (tumor necrosis factor) and interleukin-1, two cytokines with diverse and seemingly paradoxical biological activities. The localized release and action of these cytokines could account for the coordinated removal and replacement of senescent extracellular matrix components in normal tissue homeostasis.

MeSH Terms
Glycosylation Humans Interleukin-1/biosynthesis,genetics Kinetics Membrane Glycoproteins/physiology Monocytes/metabolism Protein Biosynthesis RNA, Messenger/genetics Tumor Necrosis Factor-alpha/biosynthesis,genetics
Chemicals
Interleukin-1 Membrane Glycoproteins RNA, Messenger Tumor Necrosis Factor-alpha
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Vlassara H
Laboratory of Medical Biochemistry, Rockefeller University, New York, NY 10021.
Brownlee M
Manogue K R
Dinarello C A
Pasagian A
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1988-06-10
Pages
1546-8
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIAID NIH HHS · R01-AI15674 · United States
NIADDK NIH HHS · R01-AM19655 · United States
NIADDK NIH HHS · R01-AM33861 · United States
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