Department of Anesthesiology, Amsterdam UMC, VU University, Amsterdam, The Netherlands.
Department of Physiology, Amsterdam UMC, VU University, Amsterdam, The Netherlands.
PLoS One. 2023 Nov 16;18(11):e0293673. doi: 10.1371/journal.pone.0293673. eCollection 2023.
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.
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.
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.
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.
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。
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。
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。
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。