Heat shock protein 72 restores cyclic AMP accumulation after heat shock in N18TG2 cells.

Abstract:

:Although there are several reports on the alteration of intracellular signal transduction during heat shock in somatic cells, the long term effects of heat shock on neuronal cells remain unknown. In this report, we investigated cyclic AMP (cAMP) accumulation and the expression of heat shock proteins following heat shock in mouse neuroblastoma N18TG2 cells. Basal cAMP accumulation, or that stimulated by serotonin (10 microM), cholera toxin (1 microg/ml), and forskolin (1 microM) was suppressed at 0, 3, and 6 h following heat shock (45 degrees C for 30 min). The cAMP levels were restored at 15 and 24 h after heat shock, corresponding with the expression of stress-induced heat shock protein 72 (HSP72). Quercetin, an inhibitor of HSP expression, decreased the expression of HSP72 and inhibited the recovery of cAMP levels 24 h after heat shock. Quercetin also decreased the basal expression of the constitutive heat shock cognate protein 70 (HSC70) and suppressed cAMP accumulation in non-heat shocked cells. These results suggest that stress-induced HSP72 restores cAMP accumulation to control levels following heat shock and that constitutive HSC70 is related to cAMP levels in non-stress conditions.

journal_name

Brain Res

journal_title

Brain research

authors

Zensho H,Nishida A,Shimizu M,Uchitomi Y,Yamawaki S

doi

10.1016/s0006-8993(98)00072-9

subject

Has Abstract

pub_date

1998-04-20 00:00:00

pages

278-83

issue

1-2

eissn

0006-8993

issn

1872-6240

pii

S0006-8993(98)00072-9

journal_volume

790

pub_type

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