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肺泡上皮细胞条件培养基对血管内皮细胞损伤的影响

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目的 观察脂多糖(LPS)诱导的肺泡上皮细胞条件培养基对血管内皮细胞炎症反应及细胞损伤的影响,探讨其机制。方法 以LPS诱导的Ⅱ型肺泡上皮细胞(A549)条件培养基为刺激物,建立人脐静脉内皮细胞(HUVEC)损伤模型。采用细胞增殖与毒性检测试剂盒(CCK-8)检测 0%(空白组)、12。5%、25%、50%、75%、100%不同浓度A549 细胞条件培养基培养 6、12、24 和 48h对HUVEC活性的影响;酶联免疫吸附试验(ELISA)检测A549 细胞条件培养基对HUVEC炎症因子[白细胞介素-6(IL-6)、肿瘤坏死因子-α(TNF-α)]、血管活性物质[血管内皮生长因子(VEGF)、内皮素-1(ET-1)]水平的影响;鬼笔环肽染色法观察A549 细胞条件培养基对HUVEC形态的影响;蛋白质免疫印迹试验(Western blotting)检测A549 细胞条件培养基对HUVEC蛋白激酶B/核转录因子-κB(AKT/NF-κB)通路相关蛋白表达的影响。结果 与空白组相比,12。5%、25%、50%浓度的A549 细胞条件培养基作用 6、12、24 h对HUVEC活性无影响,作用 48h后HUVEC活性显著降低,故选择 12。5%、25%、50%浓度A549 细胞条件培养基作用 24h为诱导条件进行后续实验。与空白组比较,12。5%和 50%条件培养基组IL-6 水平显著升高(ng/L:2438。95±64。89、3036。41±96。69比 1736。75±20。99,均P<0。05),12。5%和 25%条件培养基组TNF-α水平显著升高(ng/L:174。08±11。09、81。37±8。17比50。03±0。26,均P<0。01),12。5%、25%和50%条件培养基组VEGF、ET-1水平均显著升高[VEGF(ng/L):173。60±41。44、192。49±12。38、318。89±27。90 比 66。68±19。65,ET-1(ng/L):54。88±1。37、36。69±0。29、24。07±0。73 比 10。67±0。25,均P<0。01]。鬼笔环肽染色结果显示,25%浓度A549 细胞条件培养基诱导的HUVEC细胞形态不规则,大小不均匀,排列紊乱,间隙变宽,微丝结构密集且不清晰,细胞膜呈锯齿样;25%条件培养基组鬼笔环肽染色的细胞荧光强度较空白组显著增加(67205。60±3430。40比56272。67±7650。95,P<0。05)。Western blotting结果显示,与空白组比较,12。5%、25%、50%条件培养基组HUVEC磷酸化NF-κB抑制因子α(p-IκBα)表达显著降低(p-IκBα/IκBα:0。38±0。08、0。67±0。12、0。31±0。07比1。00±0。00,均P<0。01),磷酸化AKT(p-AKT)、VEGF表达显著升高(p-AKT/AKT:1。50±0。18、1。42±0。27、1。61±0。14 比 1。00±0。00,EGF/GAPDH:1。37±0。10、1。53±0。22、1。40±0。12比1。00±0。00,均P<0。05),25%条件培养基组磷酸化NF-κB p65(p-P65)表达显著升高(p-P65/P65:1。45±0。14 比 1。00±0。00,P<0。05)。结论 LPS诱导的肺泡上皮细胞条件培养基可通过激活AKT/NF-κB通路诱导内皮细胞损伤。
Effects of conditioned medium of alveolar epithelial cells on vascular endothelial cell damage
Objective To observe the effect of lipopolysaccharide(LPS)induced conditioned medium of alveolar epithelial cells on the inflammatory response and cell damage of vascular endothelial cells,and explore its mechanism.Methods The LPS induced typeⅡalveolar epithelial cells(A549)conditioned medium was used as a stimulus to induce human umbilical vein endothelial cells(HUVEC)damage.The cell counting kit-8(CCK-8)was used to detect the effect of 0%(blank group),12.5%,25%,50%,75%and 100%A549 cell conditioned medium cultured for 6,12,24 and 48 hours on the cell viability of HUVEC.Enzyme-linked immunosorbent assay(ELISA)was used to detect the levels of inflammatory factors[interleukin-6(IL-6),tumor necrosis factor-α(TNF-α)]and vasoactive substances[vascular endothelial growth factor(VEGF),endothelin-1(ET-1)]in the supernatant.Phalloidin staining was used to observe the effects of A549 cells conditioned medium on cell morphology.The expressions of protein kinase B/nuclear factor-κB(AKT/NF-κB)pathway in HUVEC induced by conditioned medium was detected by Western blotting.Results Compared with the blank group,A549 cells conditioned medium with concentrations of 12.5%,25%,and 50%had no significant effects on cell viability of HUVEC after 6,12,and 24 hours,but the activity of HUVEC decreased significantly after 48 hours.Therefore,12.5%,25%,50%A549 cell conditioned medium stimulated for 24 hours was selected as the induction condition for follow-up experiments.Compared with the blank group,the level of IL-6 was significantly increased in 12.5%and 50%conditioned medium groups(ng/L:2438.95±64.89,3036.41±96.69 vs.1736.75±20.99,both P<0.05),the level of TNF-α was significantly increased in 12.5%and 25%conditioned medium groups(ng/L:174.08±11.09,81.37±8.17 vs.50.03±0.26,both P<0.01),the levels of VEGF and ET-1 were significantly increased in 12.5%,25%and 50%conditioned medium groups[VEGF(ng/L):173.60±41.44,192.49±12.38,318.89±27.90 vs.66.68±19.65;ET-1(ng/L):54.88±1.37,36.69±0.29,24.07±0.73 vs.10.67±0.25,all P<0.01].Phalloidin staining showed that HUVEC induced by 25%A549 cells conditioned medium were irregular in shape,uneven in size,disordered in arrangement,widened in gap,dense and unclear in microfilament structure and serrated in cell membrane.Furthermore,the average fluorescence intensity of 25%conditioned medium group significantly increased compared to the blank group(67205.60±3430.40 vs.56272.67±7650.95,P<0.05).Western blotting showed that compared with the blank group,the expression of HUVEC cells phosphonated inhibitor α of NF-κB(p-IκBα)was significantly decreased in the 12.5%,25%,and 50%conditioned medium groups(p-IκBα/IκBα:0.38±0.08,0.67±0.12,0.31±0.07 vs.1.00±0.00,all P<0.01),the expressions of phosphonated-AKT(p-AKT)and VEGF were significantly increased(p-AKT/AKT:1.50±0.18,1.42±0.27,1.61±0.14 vs.1.00±0.00,VEGF/GAPDH:1.37±0.10,1.53±0.22,1.40±0.12 vs.1.00±0.00,all P<0.05),the expression of phosphonated NF-κB p65(p-P65)was significantly increased in the 25%conditioned medium group(p-P65/P65:1.45±0.14 vs.1.00±0.00,P<0.05).Conclusion LPS induced conditional culture medium of alveolar epithelial cells induced endothelial cell damage via activating AKT/NF-κB pathway.

Chronic obstructive pulmonary diseaseConditional medium co-cultureAlveolar epithelial cellVascular endothelial cell damageInflammatory responseProtein kinase B/nuclear factor-κB pathway

杨静帆、李海博、秦燕勤、李建生

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河南中医药大学中医药科学院,郑州 450046

河南中医药大学 河南省中医药防治呼吸病重点实验室 呼吸疾病中医药防治省部共建协同创新中心,郑州 450046

河南中医药大学第一附属医院呼吸与危重症医学科,郑州 450003

慢性阻塞性肺疾病 条件培养基共培养法 肺泡上皮细胞 血管内皮细胞损伤 炎症反应 蛋白激酶B/核转录因子-κB通路

国家自然科学基金国家自然科学基金河南省科技攻关项目河南省高等学校重点科研项目河南省博士后科研项目

821046628197382222210231014122A360007202101046

2024

中华危重病急救医学
中华医学会

中华危重病急救医学

CSTPCD北大核心
影响因子:3.049
ISSN:2095-4352
年,卷(期):2024.36(2)
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