In vitro intermittent hypoxia: challenges for creating hypoxia in cell culture

被引:32
作者
Baumgardner, JE
Otto, CM
机构
[1] Hosp Univ Penn, Dept Anesthesia, Philadelphia, PA 19104 USA
[2] SpectruMedix LLC, State Coll, PA 16803 USA
[3] Univ Penn, Sch Vet Med, Dept Clin Studies Philadelphia, Philadelphia, PA 19104 USA
[4] Univ Penn, Ctr Sleep & Resp Neurobiol, Philadelphia, PA 19104 USA
关键词
cell; culture; intermittent hypoxia; disease; sleep apnea; hypoxia; intermittent; methods; cell culture; sleep; apnea;
D O I
10.1016/S1569-9048(03)00077-6
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Intermittent hypoxia has been implicated in morbidities associated with sleep apnea, and may be a novel cellular signal for inflammation [J. Appl. Physiol. 90 (2001) 1986]. Standard cell culture has two major limitations for studying the effects of steady-state Po-2 and intermittent hypoxia. First, convective mixing in the culture media can be variable, making precise control of cellular Po-2 difficult. Second, diffusion of oxygen through the culture media slows changes in cellular Po-2 after rapid changes in the gas phase Po-2. Our estimates of diffusional transients for standard cell culture suggest significant restrictions in the ability to cycle Po, at frequencies relevant to intermittent hypoxia. We present a novel system for forced convection cell culture with adherent cells inside capillary tubing. Steady state cellular Po-2 is regulated to an accuracy of approximately 1 Torr. The response time for cycling of Po-2 is less than 1.6 sec. This system is ideally suited for studies of intermittent hypoxia in adherent cells. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:131 / 139
页数:9
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