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
AUTHORS (8)
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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