Subcellular localization of myosin-V in the B16 melanoma cells, a wild-type cell line for the dilute gene

被引:82
作者
Nascimento, AAC
Amaral, RG
Bizario, JCS
Larson, RE
Espreafico, EM
机构
[1] UNIV SAO PAULO,FAC MED RIBEIRAO PRETO,DEPT MORPHOL,BR-14049900 RIBEIRAO PRET,SP,BRAZIL
[2] UNIV SAO PAULO,FAC MED RIBEIRAO PRETO,DEPT BIOCHEM,BR-14049900 RIBEIRAO PRET,SP,BRAZIL
[3] UNIV FED GOIAS,FAC FARMACEUT SCI,BR-74021070 GOIANIA,GO,BRAZIL
关键词
D O I
10.1091/mbc.8.10.1971
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The discovery that the dilute gene encodes a class V myosin led to the hypothesis that this molecular motor is involved in melanosome transport and/or dendrite outgrowth in mammalian melanocytes. The present studies were undertaken to gain insight into the subcellular distribution of myosin-Ti in the melanoma cell line B16-F10, which is wildtype for the dilute gene. Immunofluorescence studies showed some degree of superimposed labeling of myosin-V with melanosomes that predominated at the cell periphery. A subcellular fraction highly enriched in melanosomes was also enriched in myosin-V based on Western blot analysis. Immunoelectron microscopy showed myosin-V labeling associated with melanosomes and other organelles. The stimulation of B16 cells with the ar-melanocyte-stimulating hormone led to a significant increase in myosin-V expression. This is the first evidence that a cAMP signaling pathway might regulate the dilute gene expression. Immunofluorescence also showed an intense labeling of myosin-V independent of melanosomes that was observed within the dendrites and at the perinuclear region. Although the results presented herein are consistent with the hypothesis that myosin-V might act as a motor for melanosome translocation, they also suggest a broader cytoplasmic function for myosin-V, acting on other types of organelles or in cytoskeletal dynamics.
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页码:1971 / 1988
页数:18
相关论文
共 48 条
[41]  
STURTZ CL, 1994, MODERN PATHOL, V7, P842
[42]   The dilute-lethal (d(l)) gene attacks a Ca2+ store in the dendritic spine of Purkinje cells in mice [J].
Takagishi, Y ;
Oda, S ;
Hayasaka, S ;
DekkerOhno, K ;
Shikata, T ;
Inouye, M ;
Yamamura, H .
NEUROSCIENCE LETTERS, 1996, 215 (03) :169-172
[43]   DOES THE INTRODUCTION OF A NEW PLAYER, THE ENDOPLASMIC-RETICULUM, CREATE MORE-OR-LESS CONFUSION IN UNDERSTANDING THE MECHANISM(S) OF PIGMENTARY ORGANELLE TRANSLOCATIONS [J].
TAYLOR, JD .
PIGMENT CELL RESEARCH, 1992, 5 (02) :49-57
[44]   ELECTROPHORETIC TRANSFER OF PROTEINS FROM POLYACRYLAMIDE GELS TO NITROCELLULOSE SHEETS - PROCEDURE AND SOME APPLICATIONS [J].
TOWBIN, H ;
STAEHELIN, T ;
GORDON, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (09) :4350-4354
[45]   Function of myosin-V in filopodial extension of neuronal growth cones [J].
Wang, FS ;
Wolenski, JS ;
Cheney, RE ;
Mooseker, MS ;
Jay, DG .
SCIENCE, 1996, 273 (5275) :660-663
[46]  
WOLFF K, 1973, YALE J BIOL MED, V46, P384
[47]  
Wu XF, 1997, J CELL SCI, V110, P847
[48]   3 MODES OF MELANOSOME TRANSFERS IN CAUCASIAN FACIAL SKIN - HYPOTHESIS BASED ON AN ULTRASTRUCTURAL-STUDY [J].
YAMAMOTO, O ;
BHAWAN, J .
PIGMENT CELL RESEARCH, 1994, 7 (03) :158-169