INTRACELLULAR-LOCALIZATION OF HEAT-SHOCK MESSENGER-RNAS (HSC7O AND HSP70) TO NEURAL CELL-BODIES AND PROCESSES IN THE CONTROL AND HYPERTHERMIC RABBIT BRAIN

Citation
Ja. Foster et Ir. Brown, INTRACELLULAR-LOCALIZATION OF HEAT-SHOCK MESSENGER-RNAS (HSC7O AND HSP70) TO NEURAL CELL-BODIES AND PROCESSES IN THE CONTROL AND HYPERTHERMIC RABBIT BRAIN, Journal of neuroscience research, 46(6), 1996, pp. 652-665
Citations number
48
Categorie Soggetti
Neurosciences
ISSN journal
03604012
Volume
46
Issue
6
Year of publication
1996
Pages
652 - 665
Database
ISI
SICI code
0360-4012(1996)46:6<652:IOHM(A>2.0.ZU;2-P
Abstract
Heat shock proteins are essential cellular proteins that may play impo rtant roles in cellular repair and/or protection. This report focuses on the expression of two members of the hsp70 multigene family, namely , constitutive hsc70 mRNA and stress-inducible hsp70 mRNA in the contr ol and hyperthermic rabbit brain. The intracellular localization of th ese heat shock mRNAs was examined using high-resolution nonradioactive in situ hybridization. The distribution of hsc70 mRNA and hsp70 mRNA was examined in (1) neuronal cell bodies and their dendritic processes and (2) oligodendrocytes and their cellular processes. In control ani mals, hsc70 mRNA was detected in the apical dendritic processes and ce ll bodies of cortical layer II and V neurons, CA3 and CA4 neurons, dee p cerebellar neurons, and brainstem neurons. A time course analysis of hsc70 mRNA, after a physiologically relevant increase in body tempera ture of 2,6 degrees C, revealed more distal transport of this constitu tive message into dendrites of these neuronal populations. In the same neuronal populations, basal levels of hsp70 mRNA were observed in the cell body; however, this mRNA was not detected in dendritic processes in control or hyperthermic animals. After hyperthermia, hsp70 mRNA wa s strongly induced in oligodendrocytes and transported to the processe s of these glial cells. The localization of heat shock messages in the processes of these neural cell types could provide a mechanism for lo cal control of synthesis of heat shock proteins in cellular compartmen ts that are remote from the cell body. (C) 1996 Wiley-Liss, Inc.