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PMID: 7506076 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Ligand-dependent polyubiquitination of c-kit gene product: a possible mechanism of receptor down modulation in M07e cells.

Blood ·Vol. 83 ·No. 1 ·1994-01-01 ·Pages 137-45

Miyazawa K, Toyama K, Gotoh A, Hendrie PC, Mantel C, Broxmeyer HE

Abstract

Quantities of proteins in cells are balanced by protein synthesis and degradation. Protein ubiquitination is an important adenosine-triphosphate dependent proteolytic pathway for "short-lived" proteins. We show that soluble steel-factor (SLF) stimulation at 37 degrees C rapidly induced polyubiquitination of c-kit protein in growth-factor-dependent human-myeloid cell line M07e, resulting in smeared, retarded migration of c-kit protein in sodium dodecyl sulfate-polyacrylamide gel electrophoresis in the molecular weight region of 145 kD. Receptor ubiquitination was almost completely absent when cells were treated with SLF at 4 degrees C or at 37 degrees C in the presence of 0.2% sodium azide, or when the cells were pretreated with anti-c-kit monoclonal antibody or genistein, a tyrosine-kinase inhibitor. This suggested that c-kit ubiquitination was ligand dependent and appeared to require intrinsic tyrosine-kinase activation of the c-kit protein. Flow-cytometric analysis of c-kit expression on the cell surface of M07e cells showed down modulation of c-kit within 5 minutes after soluble-SLF treatment at 37 degrees C. However, rapid receptor down modulation was almost completely suppressed when cells were treated with SLF at 4 degrees C or at 37 degrees C in the presence of 0.2% sodium azide, conditions that concomitantly suppressed polyubiquitination of c-kit protein. In addition, these conditions almost completely suppressed radiolabeled SLF (125I-SLF) internalization after ligand-receptor interaction. Pulse-chase studies of 35S-methionine-labeled c-kit protein showed that SLF stimulation at 37 degrees C strikingly enhanced c-kit degradation (T1/2; approximately 20 minutes) compared with that in cells stimulated with SLF at 4 degrees C or at 37 degrees C with 0.2% sodium azide. However, in the presence of chloroquine, which blocks lysosomal degradation, this ligand-induced c-kit degradation at 37 degrees C was only suppressed in part. These data suggest that SLF-induced polyubiquitination of the c-kit receptor protein may play a role in regulation of c-kit-encoded protein-receptor expression in M07e cells.

MeSH Terms
Amino Acid Sequence Antibodies, Monoclonal/immunology Azides/pharmacology Cell Line Down-Regulation Genistein Hematopoietic Cell Growth Factors/metabolism,pharmacology Humans Isoflavones/pharmacology Molecular Sequence Data Proto-Oncogene Proteins/metabolism Proto-Oncogene Proteins c-kit Receptor Protein-Tyrosine Kinases/metabolism Receptors, Colony-Stimulating Factor/metabolism Sodium Azide Stem Cell Factor Temperature Ubiquitins/metabolism
Chemicals
Antibodies, Monoclonal Azides Hematopoietic Cell Growth Factors Isoflavones Proto-Oncogene Proteins Receptors, Colony-Stimulating Factor Stem Cell Factor Ubiquitins Sodium Azide Genistein Proto-Oncogene Proteins c-kit Receptor Protein-Tyrosine Kinases
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Miyazawa K
First Department of Internal Medicine (Hematology/Oncology), Tokyo Medical College, Japan.
Toyama K
Gotoh A
Hendrie P C
Mantel C
Broxmeyer H E
Article Info
Journal
Blood
Abbr.
Blood
ISSN
0006-4971
Published
1994-01-01
Pages
137-45
Language
English
Region
United States
NLM ID
7603509
Subset
IM
Grants
NHLBI NIH HHS · R01 HL46549 · United States
NHLBI NIH HHS · R01 HL49202 · United States
NCI NIH HHS · R37 CA36464 · United States
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