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[大鼠肺微血管内皮细胞通透性系数的测量方法]

[Methods for measurement of permeability coefficient of pulmonary microvascular endothelial cells in rat].

作者信息

You Qing-hai, Gao Lei, Yue Yang, Sun Geng-yun

机构信息

Department of Respiratory Medicine, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China

出版信息

Zhongguo Wei Zhong Bing Ji Jiu Yi Xue. 2011 Sep;23(9):547-50.

Abstract

OBJECTIVE

To explore an optimal method for the measurement of pulmonary microvascular endothelial cell (PMVEC) permeability coefficient.

METHODS

A monolayer of rat PMVEC model was constructed by culturing a cell suspension on transwell filter or polycarbonate filter membrane. After the state of confluence of cells was affirmed with epithelial volt-ohm meter or inverted microscope, the permeability coefficient was determined by means of transendothelial electrical resistance (TER), fluoresceinisothiocyanate-dextran (Pd), and permeation of Hanks solution (Lp) across monolayers. Meanwhile,changes in PMVEC permeability expressed by the ratio of the observed value and the original value were observed after lipopolysaccharide (LPS) challenge for 0. 5 hour or 2 hours.

RESULTS

The cells reached the state of confluence as observed under inverted microscope on the third day post-seeding, and the TER and Pdat this time-point were C(39. 45 ± 3. 96) ( 2 cm2] and [(8. 52 + 0. 50) X 10-6cm/s], respectively. After PMVEC were seeded on transwell filters, the TER increased steadily in a time-dependent manner after seeding of PMVEC, reaching the summit at the fourth day post-seeding C(49. 84 ± 3. 93)f " cm2].Under the natural state, the TER, Pd and Lp of confluent PMVEC monolayers were (49.84 ±3.93) ·.* cm2, (6.15±0.63) X 106 cm/s and (6.80 + 0.62) X10< cm * s-' * cm HZO-', respectively.After PMVEC monolayers were challenged with 10 mg/L LPS for both 0. 5 hour and 2 hours, there was significant decrease in the permeability coefficient as measured by TER (0. 87+ 0. 03, 0.45 0. 04 vs. 1.00+0.08, respectively, both P< 0.05), and an increase in the permeability coefficient measured by Pd (1.33±0. 11, 2.43±0. 14 vs. 1.00+0.10, respectively, both P<0. 05) and the permeability coefficient measured by Lp (1.30± 0.07, 2.38 0.15 vs. 1.00 + 0.11, respectively, both P< 0.05) when compared with the normal group.

CONCLUSION

Three methods, namely TER, Pd and Lp are available to use to assess PMVEC permeability coefficient. The combination of an inverted microscope, TER and Pd enhances the accuracy in determining PMVEC permeability coefficient, and it provides an experimental technique for studying the pathogenesis of acute lung injury in vitro.

摘要

目的

探索测量肺微血管内皮细胞(PMVEC)通透性系数的最佳方法。

方法

通过将细胞悬液接种于Transwell滤膜或聚碳酸酯滤膜上构建大鼠PMVEC单层模型。用上皮伏欧计或倒置显微镜确认细胞融合状态后,采用跨内皮电阻(TER)、异硫氰酸荧光素 - 葡聚糖(Pd)以及Hanks溶液跨单层的渗透(Lp)来测定通透性系数。同时,观察脂多糖(LPS)刺激0.5小时或2小时后,以观察值与初始值之比表示的PMVEC通透性变化。

结果

接种后第3天在倒置显微镜下观察到细胞达到融合状态,此时TER和Pd分别为(39.45±3.96)[2 cm²]和[(8.52 + 0.50)×10⁻⁶ cm/s]。PMVEC接种于Transwell滤膜后,TER在接种后呈时间依赖性稳步增加,在接种后第4天达到峰值(49.84±3.93)f“cm²]。在自然状态下,融合的PMVEC单层的TER、Pd和Lp分别为(​49.84±3.93)·.* cm²、(6.15±0.63)×10⁻⁶ cm/s和(6.80 + 0.62)×10⁻⁴ cm·s⁻¹·cmH₂O⁻¹。PMVEC单层用10 mg/L LPS刺激0.5小时和2小时后,与正常组相比,TER测量的通透性系数显著降低(分别为0.87 + 0.03、0.45 0.04 vs. 1.00 + 0.08,均P < 0.05),Pd测量的通透性系数增加(分别为1.33±0.11、2.43±0.14 vs. 1.00 + 0.10,均P < 0.05),Lp测量的通透性系数增加(分别为1.30±0.07、2.38 0.15 vs. 1.00 + 0.11,均P < 0.05)。

结论

TER、Pd和Lp这三种方法均可用于评估PMVEC通透性系数。倒置显微镜、TER和Pd相结合提高了测定PMVEC通透性系数的准确性,为体外研究急性肺损伤的发病机制提供了一种实验技术。

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