基因亚型
光学(聚焦)
计算生物学
神经科学
计算机科学
生物
遗传学
物理
基因
光学
作者
Shayna M. Mueller,Kelli McFarland White,Stuart B. Fass,Siyu Chen,Zhan Shi,Xia Ge,John A. Engelbach,Seana H Gaines,Annie R. Bice,Michael J. Vasek,Joel R. Garbow,Joseph P. Culver,Zila Martínez‐Lozada,Martine Cohen‐Salmon,Joseph D. Dougherty,Darshan Sapkota
标识
DOI:10.3389/fncel.2023.1272391
摘要
Aquaporin-4 (AQP4) is a water channel protein that links the astrocytic endfeet to the blood-brain barrier (BBB) and regulates water and potassium homeostasis in the brain, as well as the glymphatic clearance of waste products that would otherwise potentiate neurological diseases. Recently, translational readthrough was shown to generate a C-terminally extended variant of AQP4, known as AQP4x, which preferentially localizes around the BBB through interaction with the scaffolding protein α-syntrophin, and loss of AQP4x disrupts waste clearance from the brain. To investigate the function of AQP4x, we generated a novel AQP4 mouse line (AllX) to increase relative levels of the readthrough variant above the ~15% of AQP4 in the brain of wild-type (WT) mice. We validated the line and assessed characteristics that are affected by the presence of AQP4x, including AQP4 and α-syntrophin localization, integrity of the BBB, and neurovascular coupling. We compared AllX
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