Rab27a Is Required for Regulated Secretion in Cytotoxic T Lymphocytes

Hypopigmentation 0301 basic medicine Mice, Inbred C3H Secretory Vesicles Cell Membrane Serine Endopeptidases Immunologic Deficiency Syndromes Cell Polarity Golgi Apparatus Cytoplasmic Granules Cathepsin D Actins Granzymes Mice, Mutant Strains 3. Good health Mice, Inbred C57BL Cytoskeletal Proteins Mice 03 medical and health sciences Hermanski-Pudlak Syndrome Actin-Related Protein 3 Actin-Related Protein 2 Animals
DOI: 10.1083/jcb.152.4.825 Publication Date: 2002-07-26T16:46:23Z
ABSTRACT
Rab27a activity is affected in several mouse models of human disease including Griscelli (ashen mice) and Hermansky-Pudlak (gunmetal mice) syndromes. A loss of function mutation occurs in the Rab27a gene in ashen (ash), whereas in gunmetal (gm) Rab27a dysfunction is secondary to a mutation in the α subunit of Rab geranylgeranyl transferase, an enzyme required for prenylation and activation of Rabs. We show here that Rab27a is normally expressed in cytotoxic T lymphocytes (CTLs), but absent in ashen homozygotes (ash/ash). Cytotoxicity and secretion assays show that ash/ash CTLs are unable to kill target cells or to secrete granzyme A and hexosaminidase. By immunofluorescence and electron microscopy, we show polarization but no membrane docking of ash/ash lytic granules at the immunological synapse. In gunmetal CTLs, we show underprenylation and redistribution of Rab27a to the cytosol, implying reduced activity. Gunmetal CTLs show a reduced ability to kill target cells but retain the ability to secrete hexosaminidase and granzyme A. However, only some of the granules polarize to the immunological synapse, and many remain dispersed around the periphery of the CTLs. These results demonstrate that Rab27a is required in a final secretory step and that other Rab proteins also affected in gunmetal are likely to be involved in polarization of the granules to the immunological synapse.
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