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Vol. 12, Issue 11, 3307-3316, November 2001
Bernhard Nocht Institute for Tropical Medicine, D-20359 Hamburg,
Germany
The differentiation of Leishmania parasites from the
insect stage, the promastigote, toward the pathogenic mammalian stage, the amastigote, is triggered primarily by the rise in ambient temperature encountered during the insect-to-mammal transmission. We
show here that inactivation of heat shock protein (Hsp) 90, with
the use of the drugs geldanamycin or radicicol, mimics transmission and
induces the differentiation from the promastigote to the amastigote stage. Geldanamycin also induces a growth arrest of cultured
promastigotes that can be forestalled by overexpression of the
cytoplasmic Hsp90. Moreover, we demonstrate that Hsp90 serves as a
feedback inhibitor of the cellular heat shock response in
Leishmania. Our results are consistent with Hsp90
homeostasis serving as cellular thermometer for these primitive
eukaryotes, controlling both the heat shock response and morphological differentiation.
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