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作 者:杨智勇[1] 陶京[1] 周峰[1] 熊炯忻 吴河水[1] 王春友[1]
机构地区:[1]华中科技大学同济医学院附属协和医院胰腺外科,湖北省武汉市430022
出 处:《世界华人消化杂志》2007年第22期2403-2407,共5页World Chinese Journal of Digestology
基 金:国家自然科学基金资助项目;No.30600593~~
摘 要:目的:探讨高迁移率族蛋白1(HMGB1)对多形核白细胞(PMN)黏附和游出肺毛细血管内皮细胞(PCEC)的影响机制.方法:分离培养大鼠PMN和PCEC,分别加入0,10,100,1000和10 000μg/L浓度的rHMGB1与PCEC单层培养.记录PMN黏附率.在Bovden小室迁移模型中加入上述浓度的rHMGB1,观察PMN穿过PCEC的迁移率.将PMN与100μg/L的rHMGB1孵育,流式细胞仪检测其表面CD11a/CD18和CD11b/CD18的表达率.结果:随着rHMGB1浓度的增加,PMN的粘附率(2.5%±0.5%,5.1%±0.9%,10.7%±1.7%,14.6%±2.6%,25.4%±4.3%)和穿过PCEC的游出率(0%,1.1%±013%,613%±1.2%,12.4%±2.7%,14.2%±3.1%)逐渐增加,但对向下室的迁移率无影响,州MGB1可明显增加PMN表面CD11a/CD18和CD11b/CD18表达的阳性率(均P<0.05)。结论:HMGB1通过上调CD11a/CD18和CD11b/CD18的表达增加PMN对PCEC的黏附率和游出率。AIM: To observe the effect of high mobility group box 1 protein (HMGB1) on adhesion to pulmonary capillary endothelial cells (PCECs) and transendothelial migration of polymorphonuclear leucocytes (PMNs), and to investigate the mechanism involved. METHODS: PMNs and PCECs of rats were isolated and cultured. PCEC monolayers were cultured with different concentrations of rHMGB, 10, 10, 10G 1000 or 10 000 μg/L. The adhesion rate of PMNs was then detected. A migration model of a boyden chamber was used to evaluate chemotaxis of HMGB1 to PMNs. Transendothelial migration was also investigated. PMNs were cultured with 100μg/L rHMGB1 and the expression of CD11a/CD18 and CD11b/CD18 was detected by flow cytometry. RESULTS: With increasing rHMGB1 concentration, adhesion and transendothelial migration rates of PMNs gradually increased (adhesion rate, 2.5 ± 0.5%, 5.1±0.9%, 10.7 ±1.7%, 14.6 ±2.6%, and 25.4 ± 4.3%; transendothelial migration rate, 0%, 1.1% ± 0.3%, 6.3 ± 1.2%, 12.4 ± 2.7%, and 14.2 ± 3.1%). rHMGB1 could increase CD11a/CD18 and CD11b/CD18 expression of PMNs (both P 〈 0.05). CONCLUSION: HMGB1 is not a chemotactic factor for PMNs but it can promote their adhesion and transendothelial migration by increas- ing expression of CD11a/CD18 and CD11b/ CD18 on the surface of PMNs.
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