Department of Microscopy, Laboratory of Cell Biology, Institute of Biomedical Sciences, Abel Salazar (ICBAS) and Multidisciplinary Unit for Biomedical Research (UMIB), University of Porto, Portugal.
University of Beira Interior, Covilhã, Portugal.
FEBS J. 2019 Apr;286(7):1393-1406. doi: 10.1111/febs.14779. Epub 2019 Feb 18.
The process that allows cells to control their pH and bicarbonate levels is essential for ionic and metabolic equilibrium. Carbonic anhydrases (CAs) catalyse the conversion of CO to and H and are thus essential for this process. Herein, we inhibited CAs with acetazolamide - ACT and SLC-0111 - to study their involvement in the metabolism, mitochondrial potential, mitochondrial biogenesis and lipid metabolism of human Sertoli cells (hSCs), obtained from biopsies from men with conserved spermatogenesis. We were able to identify three isoforms of CAs, one mitochondrial isoform (CA VB) and two cell membrane-bound isoforms (CA IX and CA XII) in hSCs. When assessing the expression of markers for mitochondrial biogenesis, we observed a decrease in HIF-1α, SIRT1, PGC1α and NRF-1 mRNAs after all CAs were inhibited, resulting in decreased mitochondrial DNA copy numbers. This was followed by an increased production of lactate and alanine in the same conditions. In addition, consumption of glucose was maintained after inhibition of all CAs in hSCs. These results indicate a reduced conversion of pyruvate to acetyl-coA, possibly due to decreased mitochondrial function, caused by CA inhibition in hSCs. Inhibition of CAs also caused alterations in lipid metabolism, since we detected an increased expression of hormone-sensitive lipase (HSL) in hSCs. Our results suggest that CAs are essential for mitochondrial biogenesis, glucose and lipid metabolism in hSCs. This is the first report showing that CAs play an essential role in hSC metabolic dynamics, being involved in mitochondrial biogenesis and controlling lactate production.
使细胞能够控制其 pH 值和碳酸氢盐水平的过程对于离子和代谢平衡至关重要。碳酸酐酶(CA)催化 CO2 转化为 HCO3- 和 H+,因此对于这个过程是必不可少的。在此,我们用乙酰唑胺 - ACT 和 SLC-0111 抑制 CA,以研究它们在代谢、线粒体电位、线粒体生物发生和脂质代谢中的参与,这些细胞是人睾丸间质细胞(hSCs),从具有保守精子发生的男性活检中获得。我们能够在 hSCs 中鉴定出三种 CA 同工酶,一种线粒体同工酶(CA VB)和两种细胞膜结合同工酶(CA IX 和 CA XII)。在评估线粒体生物发生标志物的表达时,我们观察到在所有 CA 被抑制后,HIF-1α、SIRT1、PGC1α 和 NRF-1 mRNA 的表达减少,导致线粒体 DNA 拷贝数减少。随后,在相同条件下,乳酸和丙氨酸的产量增加。此外,在 hSCs 中抑制所有 CA 后,葡萄糖的消耗仍然保持。这些结果表明,由于 CA 抑制导致线粒体功能下降,丙酮酸向乙酰辅酶 A 的转化减少。CA 的抑制也导致脂质代谢发生改变,因为我们在 hSCs 中检测到激素敏感脂肪酶(HSL)的表达增加。我们的结果表明,CA 对于 hSCs 中的线粒体生物发生、葡萄糖和脂质代谢是必不可少的。这是第一个表明 CA 在 hSC 代谢动力学中发挥重要作用的报告,涉及线粒体生物发生和控制乳酸生成。