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女性性别可预防内皮屏障调节因子 Tie2 部分缺失的小鼠发生肾水肿,但不能预防肺水肿,而男性则相反。

Female sex protects against renal edema, but not lung edema, in mice with partial deletion of the endothelial barrier regulator Tie2 compared to male sex.

机构信息

Department of Anesthesiology, Amsterdam UMC, VU University, Amsterdam, The Netherlands.

Department of Physiology, Amsterdam UMC, VU University, Amsterdam, The Netherlands.

出版信息

PLoS One. 2023 Nov 16;18(11):e0293673. doi: 10.1371/journal.pone.0293673. eCollection 2023.

Abstract

BACKGROUND

The endothelial angiopoietin/Tie2 system is an important regulator of endothelial permeability and targeting Tie2 reduces hemorrhagic shock-induced organ edema in males. However, sexual dimorphism of the endothelium has not been taken into account. This study investigated whether there are sex-related differences in the endothelial angiopoietin/Tie2 system and edema formation.

METHODS

Adult male and female heterozygous Tie2 knockout mice (Tie2+/-) and wild-type controls (Tie2+/+) were included (n = 9 per group). Renal and pulmonary injury were determined by wet/dry weight ratio and H&E staining of tissue sections. Protein levels were studied in plasma by ELISA and pulmonary and renal mRNA expression levels by RT-qPCR.

RESULTS

In Tie2+/+ mice, females had higher circulating angiopoietin-2 (138%, p<0.05) compared to males. Gene expression of angiopoietin-1 (204%, p<0.01), angiopoietin-2 (542%, p<0.001) were higher in females compared to males in kidneys, but not in lungs. Gene expression of Tie2, Tie1 and VE-PTP were similar between males and females in both organs. Renal and pulmonary wet/dry weight ratio did not differ between Tie2+/+ females and males. Tie2+/+ females had lower circulating NGAL (41%, p<0.01) compared to males, whereas renal NGAL and KIM1 gene expression was unaffected. Interestingly, male Tie2+/- mice had 28% higher renal wet/dry weight ratio (p<0.05) compared to Tie2+/+ males, which was not observed in females nor in lungs. Partial deletion of Tie2 did not affect circulating angiopoietin-1 or angiopoietin-2, but soluble Tie2 was 44% and 53% lower in males and females, respectively, compared to Tie2+/+ mice of the same sex. Renal and pulmonary gene expression of angiopoietin-1, angiopoietin-2, estrogen receptors and other endothelial barrier regulators was comparable between Tie2+/- and Tie2+/+ mice in both sexes.

CONCLUSION

Female sex seems to protect against renal, but not pulmonary edema in heterozygous Tie2 knock-out mice. This could not be explained by sex dimorphism in the endothelial angiopoietin/Tie2 system.

摘要

背景

内皮细胞血管生成素/Tie2 系统是调节内皮细胞通透性的重要因子,靶向 Tie2 可减少雄性出血性休克引起的器官水肿。然而,内皮细胞的性别二态性尚未被考虑在内。本研究旨在探讨内皮细胞血管生成素/Tie2 系统和水肿形成是否存在性别相关差异。

方法

纳入成年雄性和雌性杂合型 Tie2 敲除小鼠(Tie2+/-)和野生型对照(Tie2+/+)(每组 9 只)。通过湿/干重比和组织切片的 H&E 染色来确定肾和肺损伤。通过 ELISA 测定血浆中的蛋白水平,通过 RT-qPCR 测定肺和肾的 mRNA 表达水平。

结果

在 Tie2+/+ 小鼠中,雌性的循环血管生成素-2 水平(138%,p<0.05)高于雄性。与雄性相比,雌性肾脏中的血管生成素-1(204%,p<0.01)和血管生成素-2(542%,p<0.001)的基因表达水平更高,但在肺中没有差异。在两个器官中,Tie2、Tie1 和 VE-PTP 的基因表达在雄性和雌性之间相似。Tie2+/+ 雌性和雄性的肾和肺湿/干重比无差异。Tie2+/+ 雌性的循环中性粒细胞明胶酶相关脂质运载蛋白(NGAL)水平(41%,p<0.01)低于雄性,而肾 NGAL 和 KIM1 基因表达不受影响。有趣的是,雄性 Tie2+/- 小鼠的肾湿/干重比(p<0.05)比 Tie2+/+ 雄性高 28%,而这种情况在雌性和雄性的肺中均未观察到。Tie2 的部分缺失不影响循环血管生成素-1 或血管生成素-2,但雄性和雌性 Tie2+/- 小鼠的可溶性 Tie2 分别比 Tie2+/+ 小鼠低 44%和 53%。在两性 Tie2+/- 和 Tie2+/+ 小鼠中,肾和肺的血管生成素-1、血管生成素-2、雌激素受体和其他内皮屏障调节剂的基因表达无差异。

结论

雌性似乎能保护杂合型 Tie2 敲除小鼠的肾脏免受水肿,但不能保护肺免受水肿。这不能用内皮细胞血管生成素/Tie2 系统的性别二态性来解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/544a/10653528/e82965bdbde7/pone.0293673.g001.jpg

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