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Expression and role of HIF-1α and HIF-2α in tissue regeneration: a study of hypoxia in house gecko tail regeneration

机译:HIF-1α和HIF-2α在组织再生中的表达及作用:HUSE GECKO尾再生缺氧研究

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The house gecko (Hemidactylus platyurus) has evolved the ability to autotomize its tail when threatened. The lost part is then regrown via epimorphic regeneration in a process that requires high energy and oxygen levels. Oxygen demand is therefore likely to outstrip supply and this can result in relative hypoxia in the tissues of the regenerating tail. The hypoxic state is stabilized by the Hypoxia Inducible Factor-1α (HIF-1α) and HIF-2α proteins. We induced tail autotomy in 30 mal H. platyurus adults using a standard procedure and then collected samples of the regenerated tail tissue on days 1, 3, 5, 8, 10, 13, 17, 21, 25, and 30 post autotomy. For each sample, mRNA expression was analyzed by qPCR, proteins were analyzed using Western Blot tests and immunohistochemistry, and the histological structure was analyzed using Hematoxylin and Eosin staining. On day 1, HIF-1α mRNA expression increased and the tissue was dominated by leucocyte and erythrocyte cells. HIF-1α mRNA expression peaked on day 3, at which time some cells were actively proliferating, migrating, and differentiating. At the same time as HIF-1α expression decreased, HIF-2α mRNA expression increased, as did overall cellular activity. HIF-2α expression increased more gradually but was present over a longer period of time than HIF-1α. We hypothesize that HIF-1α helps to initially stimulate the tissue regeneration process while HIF-2α functionally takes over the role of HIF-1α after HIF-1α succumbs to the oxygen conditions, but we suspect that both HIF-1α and HIF-2α play a role in overcoming the tissue’s hypoxic state.
机译:房子壁虎(Hemidactylus platyurus)在受到威胁时演变出了自动调整其尾巴的能力。然后,在需要高能量和氧水平的过程中,通过映像再生重新重新重新生长丢失的部分。因此,氧气需求可能会出现超过供应,这可能导致再生尾部组织中的相对缺氧。缺氧状态被缺氧诱导因子-1α(HIF-1α)和HIF-2α蛋白质稳定。我们使用标准程序在30 mal H. platyurus成年人中诱导尾动术,然后在第1,3,5,8,10,13,17,21,25和30天后收集再生尾部组织的样品。对于每个样品,通过QPCR分析mRNA表达,使用蛋白质印迹试验和免疫组织化学分析蛋白质,并使用苏木精和曙红染色分析组织学结构。在第1天,HIF-1αmRNA表达增加,组织由白细胞和红细胞细胞主导。 HIF-1αmRNA表达在第3天达到峰值,此时一些细胞正在主动增殖,迁移和分化。与HIF-1α表达降低的同时,HIF-2αmRNA表达增加,总细胞活性如同均等。 HIF-2α表达更逐渐增加,但存在于比HIF-1α更长的时间较长的时间。我们假设HIF-1α有助于最初刺激组织再生过程,而HIF-2α功能齐全地接管HIF-1α屈服于氧气条件后HIF-1α的作用,但我们怀疑HIF-1α和HIF-2α都在播放在克服组织的缺氧状态方面的作用。

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