Grover A K, Samson S E, Misquitta C M
Department of Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.
Am J Physiol. 1997 Aug;273(2 Pt 1):C420-5. doi: 10.1152/ajpcell.1997.273.2.C420.
Sarco(endo)plasmic reticulum Ca2+ pumps are encoded by genes SERCA1, SERCA2, and SERCA3. Most tissues express SERCA2 Ca2+ pumps (splice SERCA2b) which are inactivated by reactive oxygen. In contrast, SERCA3 is expressed in tissues such as tracheal epithelium, mast cells, lymphoid cells, and aortic endothelium, which are frequently exposed to oxidative stress. Therefore, we compared SERCA3 and SERCA2b proteins for their sensitivity to oxidation. We isolated microsomes from HEK-293 cells overexpressing SERCA3 or SERCA2b. We incubated the microsomes with different concentrations of hydrogen peroxide and then determined Ca2+ pump activities in them in the following three assay systems: ATP-dependent oxalate-stimulated azide-insensitive 45Ca2+ uptake by the microsomal vesicles, Ca(2+)-Mg(2+)-ATPase, and Ca(2+)-dependent acylphosphate formation. Peroxide inhibited the pump activities in microsomes with half-maximal inhibitory concentration (IC50) values of 69 +/- 14, 66 +/- 13, and 84 +/- 15 microM for the 45Ca2+ uptake, Ca(2+)-Mg(2+)-ATPase, and the acylphosphate formation reactions, respectively. However, for microsomes from SERCA3-expressing cells, the corresponding values of IC50 for peroxide were 274 +/- 47, 857 +/- 110, and 746 +/- 40 microM. Thus, in each assay system, the resistance to inactivation by peroxide was significantly (P < 0.05) higher for the SERCA3 protein than for SERCA2b. The SERCA3 resistance to oxidants may aid the cells expressing it to function during exposure to oxidative stress.
肌(内)质网Ca2+泵由SERCA1、SERCA2和SERCA3基因编码。大多数组织表达SERCA2 Ca2+泵(剪接体SERCA2b),其会被活性氧灭活。相比之下,SERCA3在气管上皮、肥大细胞、淋巴细胞和主动脉内皮等经常暴露于氧化应激的组织中表达。因此,我们比较了SERCA3和SERCA2b蛋白对氧化的敏感性。我们从过表达SERCA3或SERCA2b的HEK-293细胞中分离微粒体。我们将微粒体与不同浓度的过氧化氢孵育,然后在以下三种测定系统中测定其中Ca2+泵的活性:微粒体囊泡对ATP依赖的草酸盐刺激的叠氮化物不敏感的45Ca2+摄取、Ca(2+)-Mg(2+)-ATP酶以及Ca(2+)-依赖的酰基磷酸形成。过氧化物抑制微粒体中的泵活性,对于45Ca2+摄取、Ca(2+)-Mg(2+)-ATP酶和酰基磷酸形成反应,其半数最大抑制浓度(IC50)值分别为69±14、66±13和84±15μM。然而,对于表达SERCA3的细胞的微粒体,过氧化物的相应IC50值为274±47、857±110和746±40μM。因此,在每个测定系统中,SERCA3蛋白对过氧化物灭活的抗性显著(P<0.05)高于SERCA2b。SERCA3对氧化剂的抗性可能有助于表达它的细胞在暴露于氧化应激期间发挥功能。