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ZAP-70 directly enhances IgM signaling in chronic lymphocytic leukemia.
- Source :
-
Blood [Blood] 2005 Mar 01; Vol. 105 (5), pp. 2036-41. Date of Electronic Publication: 2004 Oct 28. - Publication Year :
- 2005
-
Abstract
- Chronic lymphocytic leukemia (CLL) B cells that express unmutated immunoglobulin heavy-chain variable region genes (IgV(H)) generally express ZAP-70, in contrast to normal B cells or most CLL cases with mutated IgV(H). Following IgM ligation, ZAP-70+ CLL cells had significantly higher levels of phosphorylated p72(Syk), BLNK, and phospholipase-Cgamma (PLCgamma) and had greater[Ca2+]i flux than did ZAP-70-negative CLL cases, including unusual ZAP-70-negative cases with unmutated IgV(H). IgM ligation of ZAP-70-negative CLL B cells infected with an adenovirus vector encoding ZAP-70 induced significantly greater levels of phosphorylated p72(Syk), BLNK, and PLCgamma and had greater[Ca2+]i flux than did similarly stimulated, noninfected CLL cells or CLL cells infected with a control adenovirus vector. We conclude that expression of ZAP-70 in CLL allows for more effective IgM signaling in CLL B cells, a feature that could contribute to the relatively aggressive clinical behavior generally associated with CLL cells that express unmutated IgV(H).
- Subjects :
- Adaptor Proteins, Signal Transducing
B-Lymphocytes immunology
B-Lymphocytes pathology
Carrier Proteins metabolism
Enzyme Precursors metabolism
Humans
Immunoglobulin Heavy Chains
Immunoglobulin Variable Region
Intracellular Signaling Peptides and Proteins
Phospholipase C gamma
Phosphoproteins metabolism
Phosphorylation
Protein-Tyrosine Kinases metabolism
Syk Kinase
Type C Phospholipases metabolism
ZAP-70 Protein-Tyrosine Kinase
Immunoglobulin M physiology
Leukemia, Lymphocytic, Chronic, B-Cell immunology
Protein-Tyrosine Kinases physiology
Signal Transduction
Subjects
Details
- Language :
- English
- ISSN :
- 0006-4971
- Volume :
- 105
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Blood
- Publication Type :
- Academic Journal
- Accession number :
- 15514014
- Full Text :
- https://doi.org/10.1182/blood-2004-05-1715