Seniuk Anika, Thiele Jonas L, Stubbe Andra, Oser Philipp, Rosendahl Alva, Bode Marlies, Meyer-Schwesinger Catherine, Wenzel Ulrich O, Ehmke Heimo
From the Institute of Cellular and Integrative Physiology (A. Seniuk, J.L.T., A. Stubbe, P.O., C.M.-S., H.E.), University Medical Center Hamburg, Germany.
German Center for Cardiovascular Research, Partner Site Hamburg/Kiel/Lübeck (A. Seniuk, A.R., U.O.W., H.E.).
Hypertension. 2020 Apr;75(4):1110-1116. doi: 10.1161/HYPERTENSIONAHA.119.13773. Epub 2020 Feb 10.
A key finding supporting a causal role of the immune system in the pathogenesis of hypertension is the observation that knockout mice on a C57Bl/6J background (B6.Rag1), which lack functional B and T cells, develop a much milder hypertensive response to Ang II (angiotensin II) than control C57Bl/6J mice. Here, we report that we never observed any Ang II resistance of B6.Rag1 mice purchased directly from the Jackson Laboratory as early as 2009. B6.Rag1 mice displayed nearly identical blood pressure increases monitored via radiotelemetry and hypertensive end-organ damage in response to different doses of Ang II and different levels of salt intake (0.02%, 0.3%, and 3% NaCl diet). Similarly, restoration of T-cell immunity by adoptive cell transfer did not affect the blood pressure response to Ang II in B6.Rag1 mice. Full development of the hypertension-resistant phenotype in B6.Rag1 mice appears to depend on the action of yet unidentified nongenetic modifiers in addition to the absence of functional T cells.
支持免疫系统在高血压发病机制中起因果作用的一项关键发现是,观察到缺乏功能性B细胞和T细胞的C57Bl/6J背景基因敲除小鼠(B6.Rag1)对血管紧张素II(Ang II)的高血压反应比对照C57Bl/6J小鼠轻得多。在此,我们报告,早在2009年我们就从未观察到直接从杰克逊实验室购买的B6.Rag1小鼠有任何对Ang II的抵抗性。B6.Rag1小鼠在通过无线电遥测监测时,对不同剂量的Ang II和不同水平的盐摄入量(0.02%、0.3%和3% NaCl饮食)显示出几乎相同的血压升高以及高血压终末器官损伤。同样,通过过继性细胞转移恢复T细胞免疫并未影响B6.Rag1小鼠对Ang II的血压反应。B6.Rag1小鼠抗高血压表型的充分发展似乎除了依赖于功能性T细胞的缺失外,还取决于尚未确定的非遗传修饰因子的作用。