Manchenkov Tania, Pasillas Martina P, Haddad Gabriel G, Imam Farhad B
Division of Neonatology, University of California San Diego School of Medicine, La Jolla, California 92093.
Division of Respiratory Medicine, University of California San Diego School of Medicine, La Jolla, California 92093 Department of Pediatrics, University of California San Diego School of Medicine, La Jolla, California 92093 Rady Children's Hospital-San Diego, San Diego, California 92123.
G3 (Bethesda). 2015 Apr 3;5(6):1107-16. doi: 10.1534/g3.115.018010.
Severe hypoxia is a common cause of major brain, heart, and kidney injury in adults, children, and newborns. However, mild hypoxia can be protective against later, more severe hypoxia exposure via "hypoxic preconditioning," a phenomenon that is not yet fully understood. Accordingly, we have established and optimized an embryonic zebrafish model to study hypoxic preconditioning. Using a functional genomic approach, we used this zebrafish model to identify and validate five novel hypoxia-protective genes, including irs2, crtc3, and camk2g2, which have been previously implicated in metabolic regulation. These results extend our understanding of the mechanisms of hypoxic preconditioning and affirm the discovery potential of this novel vertebrate hypoxic stress model.
严重缺氧是成人、儿童和新生儿大脑、心脏和肾脏发生重大损伤的常见原因。然而,轻度缺氧可通过“缺氧预处理”对随后更严重的缺氧暴露起到保护作用,这一现象尚未完全被理解。因此,我们建立并优化了一种胚胎斑马鱼模型来研究缺氧预处理。我们采用功能基因组学方法,利用这种斑马鱼模型鉴定并验证了五个新的缺氧保护基因,包括irs2、crtc3和camk2g2,这些基因之前已被证明与代谢调节有关。这些结果扩展了我们对缺氧预处理机制的理解,并肯定了这种新型脊椎动物缺氧应激模型的发现潜力。