Departments of Physiology and Cell Biology, University of South Alabama, Mobile, Alabama.
Department of Internal Medicine, University of South Alabama, Mobile, Alabama.
Am J Physiol Lung Cell Mol Physiol. 2019 Aug 1;317(2):L188-L201. doi: 10.1152/ajplung.00544.2018. Epub 2019 May 1.
Acidosis is common among critically ill patients, but current approaches to correct pH do not improve disease outcomes. During systemic acidosis, cells are either passively exposed to extracellular acidosis that other cells have generated (extrinsic acidosis) or they are exposed to acid that they generate and export into the extracellular space (intrinsic acidosis). Although endothelial repair following intrinsic acidosis has been studied, the impact of extrinsic acidosis on migration and angiogenesis is unclear. We hypothesized that extrinsic acidosis inhibits metabolism and migration but promotes capillary-like network formation in pulmonary microvascular endothelial cells (PMVECs). Extrinsic acidosis was modeled by titrating media pH. Two types of intrinsic acidosis were compared, including increasing cellular metabolism by chemically inhibiting carbonic anhydrases (CAs) IX and XII (SLC-0111) and with hypoxia. PMVECs maintained baseline intracellular pH for 24 h with both extrinsic and intrinsic acidosis. Whole cell CA IX protein expression was decreased by extrinsic acidosis but not affected by hypoxia. When extracellular pH was equally acidic, extrinsic acidosis suppressed glycolysis, whereas intrinsic acidosis did not. Extrinsic acidosis suppressed migration, but increased Matrigel network master junction and total segment length. CRISPR-Cas9 CA IX knockout PMVECs revealed an independent role of CA IX in promoting glycolysis, as loss of CA IX alone was accompanied by decreased hexokinase I and pyruvate dehydrogenase E1α expression and decreasing migration. 2-deoxy-d-glucose had no effect on migration but profoundly inhibited network formation and increased N-cadherin expression. Thus, we report that while extrinsic acidosis suppresses endothelial glycolysis and migration, it promotes network formation.
酸中毒在危重病患者中很常见,但目前纠正 pH 值的方法并不能改善疾病预后。在系统性酸中毒中,细胞要么被动暴露于其他细胞产生的细胞外酸中毒(外在酸中毒),要么暴露于自身产生并分泌到细胞外空间的酸(内在酸中毒)。尽管已经研究了内在酸中毒后内皮修复,但外在酸中毒对迁移和血管生成的影响尚不清楚。我们假设外在酸中毒抑制代谢和迁移,但促进肺微血管内皮细胞(PMVECs)中毛细血管样网络的形成。通过滴定培养基 pH 值来模拟外在酸中毒。比较了两种类型的内在酸中毒,包括通过化学抑制碳酸酐酶(CA)IX 和 XII(SLC-0111)和缺氧来增加细胞代谢。PMVECs 在有外在和内在酸中毒的情况下将细胞内 pH 值维持在基线水平 24 小时。外在酸中毒降低了整体细胞 CA IX 蛋白表达,但缺氧没有影响。当细胞外 pH 值同样酸性时,外在酸中毒抑制糖酵解,而内在酸中毒则不抑制。外在酸中毒抑制迁移,但增加了 Matrigel 网络主连接和总片段长度。CRISPR-Cas9 CA IX 敲除 PMVECs 揭示了 CA IX 在促进糖酵解中的独立作用,因为 CA IX 的缺失本身伴随着己糖激酶 I 和丙酮酸脱氢酶 E1α表达的降低以及迁移的减少。2-脱氧-d-葡萄糖对迁移没有影响,但可显著抑制网络形成并增加 N-钙黏蛋白表达。因此,我们报告外在酸中毒抑制内皮细胞糖酵解和迁移,但促进网络形成。