CALMODULIN-RELATED CHANGES IN MICROSOMAL MEMBRANE FLUIDITY DURING LIVER-REGENERATION

Citation
L. Kopeikina et al., CALMODULIN-RELATED CHANGES IN MICROSOMAL MEMBRANE FLUIDITY DURING LIVER-REGENERATION, The Journal of surgical research, 67(2), 1997, pp. 155-162
Citations number
32
Categorie Soggetti
Surgery
ISSN journal
00224804
Volume
67
Issue
2
Year of publication
1997
Pages
155 - 162
Database
ISI
SICI code
0022-4804(1997)67:2<155:CCIMMF>2.0.ZU;2-O
Abstract
Based on our previous findings on the modifying effect of calmodulin ( CaM) on the physicochemical properties of biomembrane, we have investi gated the possible relationship between intracellular CaM content and endoplasmic reticulum (ER) membrane fluidity and function during liver regeneration. The degree of ER membrane fluidity was estimated by flu orescence polarization analysis with the 1,6-diphenyl-1,3,5-hexatriene probe. Microsomal guanylate cyclase (GC) was used as a functional par ameter. The kinetics of the increase in the ER membrane fluidity durin g liver regeneration was strictly parallel to the CaM surge and was ma tched by an increase in GC activity. The stimulative effect of splenec tomy on liver regeneration and its inhibition by Walker-256 tumor, inf erred from the corresponding alterations of CaM levels, were mirrored by the modulation in GC activity. The fluidizing effect of CaM on ER m embrane was concluded from the drop in thermotropic transition tempera ture from 28.3 +/- 1.6 degrees C in control membranes to 17.8 +/- 1.1 degrees C in membranes from regenerating livers and to 19.8 +/- 1.2 de grees C in control membranes treated with CaM. Arrhenius plots of GC a ctivity exhibited a transition temperature of 25.5 +/- 1.25 degrees C in controls, which shifted to 20.5 +/- 0.9 degrees C in ER membranes f rom regenerating livers and to 21.7 +/- 1.1 degrees C in control membr anes treated with CaM. The Hill coefficient for the allosteric activat ion of the GC by Mn . GTP decreased from 1.49 +/- 0.16 in controls to 0.93 +/- 0.085 in membranes from regenerating cells and to 0.86 +/- 0. 073 in CaM-treated membranes. Both effects of CaM were consistent with a fluidity increase in the enzyme's lipid microenvironment. The resul ts of the present study suggest that an early key event in liver regen eration may be the CaM-induced modulation of ER membrane fluidity and function. (C) 1997 Academic Press.