Berkovich A, Massaro D, Clerch L B
Department of Pediatrics, Georgetown University School of Medicine, Washington, District of Columbia 20007-2197, USA.
Am J Physiol. 1996 Dec;271(6 Pt 1):L875-9. doi: 10.1152/ajplung.1996.271.6.L875.
Treatment of rats with pertussis toxin (PTX) decreases the activity of manganese superoxide dismutase (Mn-SOD) in the lung and results in oxygen toxicity in air (L. B. Clerch, G. Neithardt, U. Spencer, J. A. Melendez, G. D. Massaro, and D. Massaro. J. Clin. Invest. 93: 2482-2489, 1994). To examine aspects of the mechanism of the PTX-induced fall in Mn-SOD activity, we injected rats with PTX (50 micrograms/kg), killed the rats 72 h later, and measured the activity, concentration, specific activity, and turnover of Mn-SOD in the lung. Treatment with PTX caused an approximately 50% fall in Mn-SOD activity and Mn-SOD concentration but no change in Mn-SOD specific activity. PTX also caused an increase in Mn-SOD mRNA concentration, a fall in Mn-SOD synthesis, and an increase in the half-life of Mn-SOD and general proteins. We conclude the PTX-induced low concentration of Mn-SOD is due to a decrease of translational efficiency. We suggest that, under normoxic conditions, signal transduction via heterotrimeric guanine nucleotide binding proteins regulates the expression of Mn-SOD at the level of translation and Mn-SOD degradation.
用百日咳毒素(PTX)处理大鼠会降低肺中锰超氧化物歧化酶(Mn-SOD)的活性,并导致在空气中出现氧中毒(L.B.克莱奇、G.奈瑟特、U.斯宾塞、J.A.梅伦德斯、G.D.马萨罗和D.马萨罗。《临床研究杂志》93:2482 - 2489,1994)。为了研究PTX诱导Mn-SOD活性下降的机制,我们给大鼠注射PTX(50微克/千克),72小时后处死大鼠,并测量肺中Mn-SOD的活性、浓度、比活性和周转率。用PTX处理导致Mn-SOD活性和Mn-SOD浓度下降约50%,但Mn-SOD比活性没有变化。PTX还导致Mn-SOD mRNA浓度增加、Mn-SOD合成下降以及Mn-SOD和一般蛋白质的半衰期增加。我们得出结论,PTX诱导的Mn-SOD低浓度是由于翻译效率降低。我们认为,在常氧条件下,通过异三聚体鸟嘌呤核苷酸结合蛋白的信号转导在翻译水平和Mn-SOD降解方面调节Mn-SOD的表达。