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Rab7 is a critical mediator in vesicular transport of tyrosinase‐related protein 1 in melanocytes
Author(s) -
HIDA Tokimasa,
SOHMA Hitoshi,
KOKAI Yasuo,
KAWAKAMI Akinori,
HIROSAKI Kuninori,
OKURA Masae,
TOSA Noriko,
YAMASHITA Toshiharu,
JIMBOW Kowichi
Publication year - 2011
Publication title -
the journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.9
H-Index - 65
eISSN - 1346-8138
pISSN - 0385-2407
DOI - 10.1111/j.1346-8138.2010.01004.x
Subject(s) - melanosome , microbiology and biotechnology , endosome , tyrosinase , golgi apparatus , biology , transport protein , melanin , chemistry , biochemistry , intracellular , endoplasmic reticulum , enzyme
How melanosomal proteins such as enzymic proteins (tyrosinase and tyrosinase‐related proteins, Tyrps) and structural protein (gp100) are transported from Golgi to melanosomal compartments is not yet fully understood. A number of small GTPases have been found to be associated with melanosomes and we have identified one of them, Rab7, a regulator of vesicular transport, organelle motility, phospholipid signaling and cytosolic degradative machinery, as being involved in the transport of Tyrp1 from Golgi to stage I melanosomes. This study further characterizes the role of Rab7 as a regulator of differential sorting of melanosomal proteins in this process. Murine melanocytes were transiently transfected with a plasmid encoding either wild‐type (Rab7WT), constitutively active (Rab7Q67L) or dominant‐negative (Rab7N125I and Rab7T22N) Rab7. Through immunocytostaining and confocal laser scanning microscopy, we quantitatively compared the bio‐distribution of melanosomal proteins between Rab7WT‐expressing cells and mutant Rab7‐expressing cells. We also characterized their differential elimination from melanosomal compartments by Rab7 by utilizing a proteasome inhibitor, MG132. Our findings indicate that Rab7 plays an important role in differential sorting of tyrosinase, Tyrp1 and gp100 in early melanogenesis cascade, and that it is more specifically involved with Tyrp1 than tyrosinase and gp100 in the trafficking from Golgi to melanosomes and the specific exit from the degradative process.