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PMID: 11119712 Published · ppublish English Journal Article

Generation and degradation of human endostatin proteins by various proteinases.

FEBS letters ·Vol. 486 ·No. 3 ·2000-12-15 ·Pages 247-51

Ferreras M, Felbor U, Lenhard T, Olsen BR, Delaissé J

Abstract

The angiogenesis inhibitor endostatin is a fragment of the NC1 domain of collagen XVIII. The generation of endostatin has been investigated only in murine hemangioendothelioma cell cultures and was ascribed to cathepsin L. Distinct endostatin-like fragments were detected in human tissues and serum. To identify proteinases able to generate such fragments, we incubated human NC1 with proteinases of all classes, including cathepsin L. Eleven out of 12 generate fragments with an N-terminus within the same 15 residue stretch as those occurring physiologically, indicating that this region is sensitive to many proteinases. None correspond to mouse endostatin. However, the efficiencies of these proteinases differed markedly. Some proteinases also proved to degrade endostatin, pointing to another regulatory loop of angiogenesis.

MeSH Terms
Angiogenesis Inhibitors/metabolism Aspartic Acid Endopeptidases/metabolism Cathepsin B/metabolism Cathepsin D/metabolism Cathepsin K Cathepsin L Cathepsins/metabolism Cell Line Collagen/chemistry,metabolism Collagen Type XVIII Cysteine Endopeptidases/metabolism Electrophoresis, Polyacrylamide Gel Endopeptidases/metabolism Endostatins Humans Matrix Metalloproteinases/metabolism Peptide Fragments/analysis,chemistry,metabolism Protein Structure, Tertiary Recombinant Proteins/chemistry,metabolism Sequence Analysis, Protein Serine Endopeptidases/metabolism
Chemicals
Angiogenesis Inhibitors Collagen Type XVIII Endostatins Peptide Fragments Recombinant Proteins Collagen Cathepsins Endopeptidases Serine Endopeptidases Cysteine Endopeptidases Cathepsin B CTSL protein, human Cathepsin L Ctsl protein, mouse CTSK protein, human Cathepsin K Ctsk protein, mouse Aspartic Acid Endopeptidases Cathepsin D Matrix Metalloproteinases
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Ferreras M
OSTEOPRO and Center for Clinical and Basic Research Herlev/Ballerup, Herlev, Denmark. mf@osteopro.dk
Felbor U
Lenhard T
Olsen B R
Delaissé J
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
ISSN
0014-5793
Published
2000-12-15
Pages
247-51
Language
English
Region
England
NLM ID
0155157
Subset
IM
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