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Issue 1086 coverIntegrated Molecular Medicine for Neuronal and Neoplastic Disorders Volume 1086 published November 2006
Ann. N.Y. Acad. Sci. 1086: 104–115 (2006). doi: 10.1196/annals.1377.010
Copyright © 2006 by the New York Academy of Sciences
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Articles by FUJIMOTO, T.
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Articles by FUJIMOTO, T.
Articles by OHSAKI, Y.

Part III. Neuroprotective Strategy for Neurodegenerative Diseases

Cytoplasmic Lipid Droplets

Rediscovery of an Old Structure as a Unique Platform

TOYOSHI FUJIMOTOa AND YUKI OHSAKIa

a Department of Anatomy and Molecular Cell Biology, Nagoya University Graduate School of Medicine, Nagoya, Japan

Key Words: lipid droplet • ADRP • Rab18 • autophagy • proteasome • apolipoprotein B • {alpha}-synuclein

Address for correspondence: Toyoshi Fujimoto, M.D., Ph.D., Department of Anatomy and Molecular Cell Biology, Nagoya University Graduate School of Medicine, 65 Tsurumai, Showa, Nagoya 466-8550, Japan. Voice: +81-52-744-2000; fax: +81-52-744-2011.  e-mail: tfujimot{at}med.nagoya-u.ac.jp

Cytoplasmic lipid droplets (LDs) exist in virtually any kind of cell. They have a core of lipid esters covered by the surface phospholipid monolayer. A number of proteins related to various cell functions are present in LDs and/or LD-rich subcellular fractions, suggesting that LDs are an independent organelle that is engaged in various cellular activities. Furthermore, a recent study suggested that LDs are a platform where the proteasomal and autophagic pathways converge. The molecular composition and architecture of LDs are discussed here, with special reference to the technical difficulties encountered when analyzing this unique organelle.




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