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1.453003 河南 新乡,新乡医学院研究生院
2.450042 郑州,联勤保障部队988医院心内科
[ 王连友,E-mail:quantin_wly@163.com WANG Lianyou, E-mail: quantin_wly@163.com
收稿:2022-07-25,
修回:2022-09-29,
纸质出版:2023-02-28
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康越, 邰苏豫, 李茂巍, 等. 钙库操纵性钙内流参与调节ox-LDL诱导的血管内皮细胞通透性改变[J]. 陆军军医大学学报, 2023,45(4):358-365.
Yue KANG, Suyu TAI, Maowei LI, et al. Store-operated calcium entry involves in regulating the hyperpermeability of endothelial cells induced by ox-LDL[J]. Journal of Army Medical University, 2023, 45(4): 358-365.
康越, 邰苏豫, 李茂巍, 等. 钙库操纵性钙内流参与调节ox-LDL诱导的血管内皮细胞通透性改变[J]. 陆军军医大学学报, 2023,45(4):358-365. DOI: 10.16016/j.2097-0927.202207164.
Yue KANG, Suyu TAI, Maowei LI, et al. Store-operated calcium entry involves in regulating the hyperpermeability of endothelial cells induced by ox-LDL[J]. Journal of Army Medical University, 2023, 45(4): 358-365. DOI: 10.16016/j.2097-0927.202207164.
目的
2
利用体外培养的人脐静脉血管内皮细胞(human umbilical vein endothelial cells,HUVECs),探讨钙库操纵性钙内流(store-operated calcium entry,SOCE)在氧化低密度脂蛋白(oxidized low-density lipoprotein,ox-LDL)诱导的血管内皮细胞通透性改变中的作用。
方法
2
体外培养HUVECs,传代3次后,用于检测跨内皮电阻(transendothelial electrical resistance,TER)的细胞随机分为对照组和不同剂量ox-LDL(10、25、50、100 μg/mL)干预组(
n
=3)。培养于载玻片上的细胞随机分为对照组和ox-LDL 24 h组、ox-LDL 48 h组,免疫荧光检测细胞骨架蛋白F-actin及细胞连接蛋白VE-cadherin的分布,免疫印迹检测VE-cadherin的含量。细胞孵育钙离子探针(Fluo-3/AM)后,激光共聚焦检测细胞内钙含量(对照组、ox-LDL组、ox-LDL+2APB组)以及SOCE(对照组、ox-LDL 24h组、ox-LDL 48 h组)。
结果
2
低剂量的ox-LDL(10、25 μg/ mL)对TER无明显影响,高剂量ox-LDL(50、100 μg/ mL)在6 h内对TER影响不明显,但在12 h引起TER降低(
P
<
0.05),此效应在24 h和48 h更加明显(
P
<
0.05)。Ox-LDL(100 μg/mL)处理后24、48 h,VE-cadherin的表达减少(
P
<
0.05),并影响F-actin的形态和分布;HUVECs的游离钙浓度显著增加(
P
<
0.05),此效应被SOCE抑制剂2-APB阻断,2-APB能够减弱ox-LDL对TER的影响。ox-LDL(100 μg/mL)处理48 h后,SOCE的振幅显著降低(
P
<
0.05)。SOCE降支速度在ox-LDL处理24 h后呈现降低趋势,而在ox-LDL处理48 h后呈显著下降(
P
<
0.05)。
结论
2
ox-LDL通过延长内皮细胞SOCE的持续时间上调细胞内游离钙浓度,影响细胞骨架的排列和细胞间连接的完整性,引起细胞通透性的增加。
Objective
2
To explore the effects of store-operated calcium entry(SOCE) on oxidized low-density lipoprotein (ox-LDL)-induced hyperpermeability in human umbilical vein endothelial cells(HUVECs).
Methods
2
HUVECs at passage 3 were divided into the control group and the ox-LDL(10
25
50 and 100 μg/mL) intervention groups (
n
=3) for the examination of transendothelial electrical resistance (TER). HUVECs cultured in slides were randomly divided into the control group
the ox-LDL 24 h group and the ox-LDL 48 h group. The distribution of F-actin and VE-cadherin were detected by immunofluorescence
and the protein content of VE-cadherin was detected by Western blotting. Incubated with calcium fluorescence probe (Fluo-3/AM)
intracellular free Ca
2+
concentration (control group
ox-LDLgroup
ox-LDL+2-APB group) and SOCE (control group
ox-LDL 24 h group
ox-LDL 48 h group) were detected by laser confocal microscopy.
Results
2
Low dose of ox-LDL(10
25 μg/mL) exerted no effect on TER. High dose of ox-LDL (50
100 μg/mL) also had no effect on TER within 6 h
but after 6 h showed no effect on TER. However
high dose of ox-LDL(50
100 μg/mL) reduced the decrease of TER in 12 h (
P
<
0.05)
and the decrease was more significant in 24 h and 48 h. After the incubation with ox-LDL(100 μg/mL) 24 h and 48 h
the expression level of VE-cadherin decreased(
P
<
0.05)
while the form and distribution of F-action changed; Intracel
lular free Ca
2+
concentration increased obviously which was interrupted by 2-APB the SOCE inhibitor (
P
<
0.05)
and the 2-APB can decrease the effect of ox-LDL on TER. After incubation with ox-LDL(100 μg/mL) 48 h
the amplitude of SOCE decreased (
P
<
0.05). The descending artery flow velocity of SOCE showed a slightly decreased trend after incubation with ox-LDL 24 h and a more significant decrease in 48 h(
P
<
0.05).
Conclusion
2
Ox-LDL up-regulate the intracellular free Ca
2+
concentration of vascular endothelial cells by extending the duration of SOCE to effect the arrangement of cytoskeleton and cell junction
which increases the cell permeability.
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