机构地区:[1]解放军总医院第一附属医院全军烧伤研究所,北京100048
出 处:《中华烧伤杂志》2010年第2期104-108,共5页Chinese Journal of Burns
基 金:国家重点基础研究发展计划(2005CB522602);国家自然科学基金(30872683、30901561)
摘 要:目的 探讨严重烫伤大鼠延迟复苏后脾脏高迁移率族蛋白B1(HMGB1)表达对调节性T淋巴细胞(Treg)表型及其介导T淋巴细胞免疫功能的影响.方法 将104只Wistar大鼠按随机对照表法分为正常对照组8只、假烫组32只、烫伤组32只、丙酮酸乙酯(EP)治疗组32只.后2组大鼠造成30%TBSAⅢ度烫伤,伤后6 h腹腔注射林格液或EP液延迟抗休克,伤后12 h起每隔12 h给予4 mL林格液或EP液至伤后48 h;假烫组除于37℃模拟烫伤外其余处理同烫伤组.于伤后1、3、5、7 d处死各致伤组大鼠,另处死正常对照组大鼠,免疫磁珠法分离大鼠脾脏CD4~+CD25~+Treg,ELISA法检测脾脏HMGBI含量及T淋巴细胞上清液中IL-2水平,采用流式细胞仪检测Treg表面分子细胞毒性T淋巴细胞相关抗原4(CTLA-4)表达,同时检测T淋巴细胞增殖活性(数据以吸光度值表示).对数据进行多组间方差分析和2组独立样本间的t检验.结果 (1)烫伤组大鼠脾脏HMGBI含量伤后1~7 d显著高于假烫组,其中第1天达峰值[(46.7±8.3)ng/mg蛋白];EP治疗组大鼠脾脏HMGBI含量伤后1~7 d明显低于烫伤组.(2)与假烫组比较,烫伤组大鼠伤后1~5 d CTLA-4表达明显增强(t值分别为10.459、12.051、4.029,P〈0.05或P〈0.01);EP治疗组伤后1~7 d CTLA-4表达较烫伤组显著降低(t值分别为2.796、9.913、9.581、10.022,P〈0.05或P〈0.01).(3)与假烫组比较,烫伤组大鼠伤后1~7 d脾脏T淋巴细胞增殖活性明显受抑,其中伤后1 d达低谷(0.167±0.059);IL-2水平伤后1~7 d显著下降,其中伤后5 d达低谷(44±24)pg/mL.与烫伤组比较,EP治疗组伤后各时相点脾脏T淋巴细胞增殖受抑状态明显缓解,且IL-2水平明显上升.结论 严重烫伤后HMGB1产生可诱导Treg向成熟发展,从而介导T淋巴细胞增殖反应低下,免疫功能抑制.EP通过抑制HMGB1的合成与释放,改善烫伤延迟复苏大鼠的细胞免疫功能紊乱.Objective To observe the influence of high mobility group box-1 protein ( HMGB1) derived from spleen on the phenotype of regulatory T lymphocytes (Treg) and HMGB1-mediated immune function in severely scalded rats after delayed resuscitation. Methods One hundred and four Wistar rats were divided into normal control group (NC, n =8) , sham scald group (SS, n =32) , scald group (S, n =32) , and ethyl pyruvate ( EP) treatment group ( EPT, n =32) according to the random comparison table. Rats in the latter 2 groups were subjected to 30% TBSA full-thickness scald, which were intraperitoneally injected with Ringer solution or EP solution at post scald hour (PSH) 6 (delayed antishock treatment) and administered with 4 mL Ringer solution or EP solution per 12 hours after PSH 12 till PSH 48. Rats in SS group were treated the same as that of S group except for sham scald with 37 ℃ water. Injured rats were sacrificed at post scald day ( PSD) 1 , 3 , 5 , 7 ( rats in NC group were also sacrificed) , and CD4^+ CD25^+ Treg were isolated from spleen with magnetic-activated cell sorting method. The content of HMGB1 in spleen and IL-2 level in supernatant were determined with ELISA. The expression of cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) on Treg was determined with flow cytometry, and the proliferation activity of T lymphocytes was also detected (recorded as absorbance value). Data were processed with analysis of variance among groups and independent samples t test. Results ( 1 ) Compared with that of rats in SS group and EPT group, the expression of splenic HMGB1 in S group increased significantly on PSD 1 through PSD 7 [peaked on PSD 1: (46.7 ±8.3) ng/mg protein]. (2) Compared with that in SS group, the expression of CTLA-4 in S group was enhanced significantly on PSD 1 through PSD 5 ( with t value respectively 10. 459, 12. 051 , 4. 029, P 〈 0.05 or P 〈0.01) ; while that in EPT group decreased significantly on PSD 1 through PSD 7 as co
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