Short-term hypoxia downregulates epithelial cell desquamation in vivo, but does not increase Pseudomonas aeruginosa adherence to exfoliated human corneal epithelial cells.

D H Ren, W M Petroll, J V Jester, J Ho-Fan, H D Cavanagh
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Abstract

Purpose: This study evaluates the effect of hypoxic and hypercapnic stress on bacterial adherence to surface corneal epithelial cells, as well as tear LDH levels, surface cell desquamation, and corneal swelling in normal human subjects.

Methods: Sixteen eyes of eight human volunteers were successively exposed to three gas mixtures (air, 100% N2, 95% N2-5% CO2) through tightly fitted goggles for six hours at two-week intervals. Exfoliated epithelial cells were collected and counted using a modified corneal irrigation chamber. Bacterial binding was determined by measuring Pseudomonas aeruginosa (PA) adherence to exfoliated corneal epithelial cells. The effects of hypoxic or hypercapnic stress on the corneal surface were also assessed by tear LDH measurement, and quantification of surface epithelial cell size and epithelial and stromal thickness were determined by in vivo confocal microscopy.

Results: Short-term precorneal hypoxia significantly decreased corneal epithelial cell desquamation. Both short-term hypoxia alone and combined with hypercapnia induced significant corneal stromal swelling (7 to 8%) but did not significantly enhance PA adherence to exfoliated human corneal epithelial cells.

Conclusions: This study demonstrates, for the first time, that short-term precorneal hypoxia downregulates corneal epithelial cell desquamation in humans. These results also demonstrate that short-term hypoxia alone or combined with hypercapnia does not significantly increase PA adherence to exfoliated epithelial cells from the human cornea. The results reveal that either longer hypoxic exposure or other interactive factor(s), including but not limited to the mechanical effect of the contact lens itself, may be required for promotion of increased epithelial cell-PA binding following lens wear in humans.

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体内短期缺氧可下调上皮细胞脱屑,但不会增加铜绿假单胞菌对脱落的人角膜上皮细胞的粘附。
目的:本研究评估缺氧和高碳酸血症应激对正常受试者角膜表面上皮细胞细菌粘附、撕裂LDH水平、表面细胞脱屑和角膜肿胀的影响。方法:8名人类志愿者的16只眼睛通过严密安装的护目镜连续暴露于三种气体混合物(空气,100% N2, 95% N2-5% CO2)中6小时,每隔两周。使用改良的角膜冲洗室收集脱落的上皮细胞并进行计数。通过测量铜绿假单胞菌(PA)对脱落的角膜上皮细胞的粘附来确定细菌结合。通过撕裂LDH测量评估低氧或高碳血症应激对角膜表面的影响,并通过体内共聚焦显微镜定量测定角膜表面上皮细胞大小和上皮和间质厚度。结果:短期角膜前缺氧可显著减少角膜上皮细胞脱屑。单独短期缺氧和联合高碳酸血症均可引起明显的角膜基质肿胀(7 - 8%),但没有显著增强PA对脱落的人角膜上皮细胞的粘附性。结论:本研究首次证明,短期角膜前缺氧可下调人类角膜上皮细胞脱屑。这些结果还表明,短期缺氧单独或联合高碳酸血症不会显著增加PA对人角膜脱落上皮细胞的粘附。结果表明,长时间的缺氧暴露或其他相互作用因素,包括但不限于隐形眼镜本身的机械效应,可能需要促进人类佩戴隐形眼镜后上皮细胞pa结合的增加。
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