Kimura J, Hayakari M, Kumano T, Nakano H, Satoh K, Tsuchida S
Second Department of Biochemistry, Hirosaki University School of Medicine, Hirosaki 036-8562, Japan.
Biochem J. 1998 Nov 1;335 ( Pt 3)(Pt 3):605-10. doi: 10.1042/bj3350605.
Since glutathione transferases (GSTs) are suggested to be involved in the prevention of tissue damage by oxidative stress, quantitative and qualitative alterations of GST forms were examined in rat skin after induction of inflammation by 0.6 and 1% 1-chloro-2, 4-dinitrobenzene (CDNB) treatment. With 0.6% CDNB, the GST activity in supernatant preparations was 1.8-fold higher than that for control skin, with most GSTs in both cases being bound to S-hexyl-GSH-Sepharose. Major GST subunits of control skin were identified as subunits 7, 4 and 2 by HPLC and chromatofocusing at pH11-7. These subunits were increased in inflamed skin by 0.6% CDNB and, in addition, the subunit 1 of the Alpha class and subunit 6, both hardly detectable in control skin, were expressed. The specific activity value for GST 7-7 from the inflamed skin by 0.6% CDNB was 2. 4-fold lower than that from control skin. However, in the case of inflamed skin after application of 1% CDNB, GST activity was decreased to 69% of the control value and most activity was recovered in fractions binding to a GSH-Sepharose but not a S-hexyl-GSH-Sepharose column. GSTs eluted from the former column demonstrated a restored capacity to bind to the latter, suggesting the GSTs in inflamed skin to be partly inactivated and that they regained activity on exposure to GSH. The Km and Vmax values for GSH of GST 4-4 from inflamed skin after 1% CDNB treatment were 6-fold and 2-fold higher, respectively, than those for the enzyme from control skin, suggesting partial enzyme modification. These results suggest that not only quantitative but also qualitative alterations of GST subunits occur with CDNB-induced inflammation in vivo.
由于谷胱甘肽转移酶(GSTs)被认为参与了预防氧化应激引起的组织损伤,因此在用0.6%和1%的1-氯-2,4-二硝基苯(CDNB)处理诱导大鼠皮肤炎症后,检测了GST形式的定量和定性变化。用0.6%的CDNB处理后,上清液制剂中的GST活性比对照皮肤高1.8倍,两种情况下大多数GST都与S-己基-GSH-琼脂糖结合。通过HPLC和在pH11-7条件下的色谱聚焦,将对照皮肤的主要GST亚基鉴定为亚基7、4和2。在用0.6%的CDNB处理的炎症皮肤中,这些亚基增加了,此外,在对照皮肤中几乎检测不到的α类亚基1和亚基6也表达了。用0.6%的CDNB处理的炎症皮肤中GST 7-7的比活性值比对照皮肤低2.4倍。然而,在应用1%的CDNB后炎症皮肤的情况下,GST活性降低到对照值的69%,并且大多数活性在与GSH-琼脂糖而非S-己基-GSH-琼脂糖柱结合的组分中恢复。从前一个柱上洗脱的GST显示出与后一个柱结合的恢复能力,这表明炎症皮肤中的GST部分失活,并且它们在暴露于GSH时恢复了活性。1%的CDNB处理后炎症皮肤中GST 4-4对GSH的Km和Vmax值分别比对照皮肤中的酶高6倍和2倍,表明酶发生了部分修饰。这些结果表明,在体内CDNB诱导的炎症中,不仅GST亚基有定量变化,而且有定性变化。