Protein synthesis during oxygen conformance and severe hypoxia in the mouse muscle cell line C2C12

被引:24
作者
Arthur, PG [1 ]
Giles, JJ [1 ]
Wakeford, CM [1 ]
机构
[1] Univ Western Australia, Dept Biochem, Nedlands, WA 6907, Australia
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2000年 / 1475卷 / 01期
基金
英国医学研究理事会;
关键词
oxygen conformance; hypoxia; muscle cell; metabolism;
D O I
10.1016/S0304-4165(00)00046-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Oxygen conformance can be described as the ability to reduce energy demand, and hence oxygen consumption, in response to a decline in oxygen availability without a decrease in the concentration of ATP. It has been proposed that oxygen conformance may enhance cellular survival at low oxygen concentrations. We demonstrate that non-contracting C2C12 cells, a mouse skeletal muscle cell line, are capable of oxygen conformance. Typically, we found oxygen consumption to decline by 30-40% as the concentration of oxygen was reduced from 100 mu M to 10 mu M. Unexpectedly. the rate of protein synthesis, a major energy consumer in the cell, did not decrease significantly during oxygen conformance. Unlike oxygen conformance, severe hypoxia (< 0.5 mu M) caused a 36% decline in the concentration of PCr, and under these conditions of energy stress, the rate of protein synthesis declined by 43%. We conclude that there are two distinct metabolic responses to declines in oxygen concentration in non-contracting C2C12 cells. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:83 / 89
页数:7
相关论文
共 25 条
[1]   A perifusion system to control oxygen concentration in cell suspensions [J].
Arthur, PG ;
Ngo, CT ;
Wakeford, CM .
ANALYTICAL BIOCHEMISTRY, 1998, 263 (02) :208-213
[2]   AUTOMATED-ANALYSIS OF CELLULAR METABOLITES AT NANOMOLAR TO MICROMOLAR CONCENTRATIONS USING BIOLUMINESCENT METHODS [J].
ARTHUR, PG ;
HOCHACHKA, PW .
ANALYTICAL BIOCHEMISTRY, 1995, 227 (02) :281-284
[3]   ANOXIA-TOLERANT HEPATOCYTES - MODEL SYSTEM FOR STUDY OF REVERSIBLE METABOLIC SUPPRESSION [J].
BUCK, LT ;
LAND, SC ;
HOCHACHKA, PW .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (01) :R49-R56
[4]   Cellular energy utilization and supply during hypoxia in embryonic cardiac myocytes [J].
Budinger, GRS ;
Chandel, N ;
Shao, ZH ;
Li, CQ ;
Melmed, A ;
Becker, LB ;
Schumacker, PT .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1996, 270 (01) :L44-L53
[5]   Hibernation during hypoxia in cardiomyocytes -: Role of mitochondria as the O2 sensor [J].
Budinger, GRS ;
Duranteau, J ;
Chandel, NS ;
Schumacker, PT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (06) :3320-3326
[6]   A HIERARCHY OF ATP-CONSUMING PROCESSES IN MAMMALIAN-CELLS [J].
BUTTGEREIT, F ;
BRAND, MD .
BIOCHEMICAL JOURNAL, 1995, 312 :163-167
[7]   An improved capillary electrophoresis method for measuring tissue metabolites associated with cellular energy state [J].
Casey, TM ;
Dufall, KG ;
Arthur, PG .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 261 (03) :740-745
[8]   DEFINING HYPOXIA - A SYSTEMS VIEW OF VO2, GLYCOLYSIS, ENERGETICS, AND INTRACELLULAR PO-2 [J].
CONNETT, RJ ;
HONIG, CR ;
GAYESKI, TEJ ;
BROOKS, GA .
JOURNAL OF APPLIED PHYSIOLOGY, 1990, 68 (03) :833-842
[9]   Molecular aspects of oxygen sensing in physiological adaptation to hypoxia [J].
CzyzykKrzeska, MF .
RESPIRATION PHYSIOLOGY, 1997, 110 (2-3) :99-111
[10]   Intracellular signaling by reactive oxygen species during hypoxia in cardiomyocytes [J].
Duranteau, J ;
Chandel, NS ;
Kulisz, A ;
Shao, ZH ;
Schumacker, PT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (19) :11619-11624