Ia binding ligands and cAMP stimulate nuclear translocation of PKC in B lymphocytes
Autor: | Louis B. Justement, M. K. Newell, John C. Cambier, Z Z Chen, J C McGuire, K L Leach |
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Rok vydání: | 1987 |
Předmět: |
medicine.medical_specialty
Cellular differentiation Chromosomal translocation Biology Ligands Antibodies Mice Mice Inbred AKR Cytosol Internal medicine Cyclic AMP medicine Animals Receptor Cells Cultured Protein Kinase C Protein kinase C Cell Nucleus B-Lymphocytes Multidisciplinary Bucladesine Histocompatibility Antigens Class II Immunoglobulin D Cell biology Kinetics Cell nucleus Endocrinology medicine.anatomical_structure Immunoglobulin M Signal transduction medicine.drug |
Zdroj: | Scopus-Elsevier |
ISSN: | 1476-4687 0028-0836 |
DOI: | 10.1038/327629a0 |
Popis: | Altered subcellular distribution and activity of protein kinase C (PKC) is associated with transmembrane signalling in a variety of systems in which receptor occupancy leads to increased hydrolysis of polyphosphoinositides. Here we report evidence that in B lymphocytes, cyclic-cAMP-generating signal transduction pathways can activate translocation of PKC from the cytosol to the nucleus. Elevated cAMP levels and translocation of PKC to the nucleus are induced by antibodies against Ia antigens in normal B lymphocytes. Further, cAMP analogues mediate the translocation of PKC to the nucleus of these cells. These findings suggest that in physiological situations, ligation of B-lymphocyte Ia molecules by helper T cells leads to increased cAMP production which in turn causes PKC translocation to the nucleus. In view of recent observations that antibodies against Ia antigens induce differentiation of B cells, we conclude that nuclear PKC may function in the regulation of gene expression. |
Databáze: | OpenAIRE |
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