Dynamics of cellular homeostasis: Recovery time for a perturbation from equilibrium

被引:10
作者
Weinstein, AM
机构
关键词
D O I
10.1016/S0092-8240(96)00093-6
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In the collecting duct in vivo, the principal cell encounters a wide range in luminal flow rate and luminal concentration of NaCl. As a consequence, there are substantial variations in the transcellular fluxes of Na+ and Cl-, conditions which would be expected to perturb cell volume and cytosolic concentrations. Several control mechanisms have been identified which can potentially blunt these perturbations, and these entail cellular regulation of the luminal membrane Na+ channel and peritubular membrane K+ and Cl- channels. To illustrate the impact of these regulated channels, a mathematical model of the principal cell of the rat cortical collecting duct has been developed, in which ion channel permeabilities are either constant or regulated. In comparison to the model with fixed permeabilities, the model with regulated channels demonstrates enhanced cellular homeostasis following steady-state variation in luminal NaCl. However, in the transient response to a cytosolic perturbation, the difference in recovery time between the models is small. An approximate analysis is presented which casts these models as dynamical systems with constant coefficients. Despite the presence of regulated ion channels, concordance of each model with its linear approximation is verified for experimentally meaningful perturbations from the reference condition. Solution of a Lyapunov equation for each linear system yields a matrix whose application to a perturbation permits explicit estimation of the time to recovery. Comparison of these solution matrices for regulated and non-regulated cells confirms the similarity of the dynamic response of the two models. These calculations suggest that enhanced homeostasis by regulated channels may be protective, without necessarily hastening recovery from cellular perturbations. (C) 1997 Society for Mathematical Biology.
引用
收藏
页码:451 / 481
页数:31
相关论文
共 29 条
[21]   VOLUME-ACTIVATED CHLORIDE PERMEABILITY CAN MEDIATE CELL-VOLUME REGULATION IN A MATHEMATICAL-MODEL OF A TIGHT EPITHELIUM [J].
STRIETER, J ;
STEPHENSON, JL ;
PALMER, LG ;
WEINSTEIN, AM .
JOURNAL OF GENERAL PHYSIOLOGY, 1990, 96 (02) :319-344
[22]   A MATHEMATICAL-MODEL OF THE RABBIT CORTICAL COLLECTING TUBULE [J].
STRIETER, J ;
STEPHENSON, JL ;
GIEBISCH, G ;
WEINSTEIN, AM .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (06) :F1063-F1075
[23]   Calcium dynamics and homeostasis in a mathematical model of the principal cell of the cortical collecting tubule [J].
Tang, YH ;
Stephenson, JL .
JOURNAL OF GENERAL PHYSIOLOGY, 1996, 107 (02) :207-230
[24]  
TEREDA Y, AM J PHYSIOL, V259, pF519
[25]   DISTRIBUTION OF CL-/HCO3- EXCHANGE AND INTERCALATED CELLS IN RABBIT CORTICAL COLLECTING DUCT [J].
WEINER, ID ;
WEILL, AE ;
NEW, AR .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL FLUID AND ELECTROLYTE PHYSIOLOGY, 1994, 267 (06) :F952-F964
[26]   Coupling of entry to exit by peritubular K+ permeability in a mathematical model of rat proximal tubule [J].
Weinstein, AM .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL FLUID AND ELECTROLYTE PHYSIOLOGY, 1996, 271 (01) :F158-F168
[27]   MATHEMATICAL-MODELS OF TUBULAR TRANSPORT [J].
WEINSTEIN, AM .
ANNUAL REVIEW OF PHYSIOLOGY, 1994, 56 :691-709
[28]   CHLORIDE TRANSPORT IN A MATHEMATICAL-MODEL OF THE RAT PROXIMAL TUBULE [J].
WEINSTEIN, AM .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (05) :F784-F798
[29]   REGULATORY ROLE OF INTRACELLULAR CALCIUM-IONS IN EPITHELIAL NA-TRANSPORT [J].
WINDHAGER, EE ;
TAYLOR, A .
ANNUAL REVIEW OF PHYSIOLOGY, 1983, 45 :519-532