4.6 Article

Influence of the Hypercapnic Tumor Microenvironment on the Viability of Hela Cells Screened by a CO2-Gradient-Generating Device

Journal

ACS OMEGA
Volume 6, Issue 40, Pages 26773-26781

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsomega.1c04422

Keywords

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Funding

  1. National Natural Science Foundation of China [81827803, 61875085, 81727804]

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The paper examines the effects of high CO2 concentrations on tumor cell proliferation and metastasis, using a gas gradient-generating apparatus to study the response of Hela cells to different levels of CO2. The results show a significant reduction in cell viability with increasing CO2 concentration and incubation time, accompanied by intracellular acidification and elevated levels of reactive oxygen species.
Carbon dioxide (CO2) levels outside of the physiological range are frequently encountered in the tumor microenvironment and laparoscopic pneumoperitoneum during clinical cancer therapy. Controversies exist regarding the biological effects of hypercapnia on tumor proliferation and metastasis concerning time frame, CO2 concentration, and cell type. Traditional control of gaseous microenvironments for cell growth is conducted using culture chambers that allow for a single gas concentration at a time. In the present paper, Hela cells were studied for their response to varying levels of CO2 in an aerogel-based gas gradient-generating apparatus capable of delivering a stable and quantitative linear CO2 profile in spatial and temporal domains. Cells cultured in the standard 96-well plate sandwiched in between the device were interfaced with the gas gradient generator, and the cells in each row were exposed to a known level of CO2 accordingly. Both the ratiometric pH indicator and theoretical modeling have confirmed the efficient mass transport of CO2 through the airpermeable aerogel monolith in a short period of time. Tumor cell behaviors in various hypercapnic microenvironments with gradient CO2 concentrations ranging from 12 to 89% were determined in terms of viability, morphology, and mitochondrial metabolism under acute exposure for 3 h and over a longer cultivation period for up to 72 h. A significant reduction in cell viability was noticed with increasing CO2 concentration and incubation time, which was closely associated with intracellular acidification and elevated cellular level of reactive oxygen species. Our modular device demonstrated full adaptability to the standard culture systems and highthroughput instruments, which provide the potential for simultaneously screening the responses of cells under tunable gaseous microenvironments.

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