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Spatiotemporal expression and transcriptional regulation of heme oxygenase and biliverdin reductase genes in zebrafish (Danio rerio) suggest novel roles during early developmental periods of heightened oxidative stress

机译:斑马鱼血红素加氧酶和胆绿素还原酶基因的时空表达和转录调控表明氧化应激加剧的早期发育过程中的新作用。

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摘要

Heme oxygenase 1 (HMOX1) degrades heme into biliverdin, which is subsequently converted to bilirubin by biliverdin reductase (BVRa or BVRb) in a manner analogous to the classic anti-oxidant glutathione-recycling pathway. To gain a better understanding of the potential antioxidant roles the BVR enzymes may play during development, the spatiotemporal expression and transcriptional regulation of zebrafish hmox1a, bvra and bvrb were characterized under basal conditions and in response to pro-oxidant exposure. All three genes displayed spatiotemporal expression patterns consistent with classic hematopoietic progenitors during development. Transient knockdown of Nrf2a did not attenuate the ability to detect bvra or bvrb by ISH, or alter spatial expression patterns in response to cadmium exposure. While hmox1a:mCherry fluorescence was documented within the intermediate cell mass, a transient location of primitive erythrocyte differentiation, expression was not fully attenuated in Nrf2a morphants, but real-time RT-PCR demonstrated a significant reduction in hmox1a expression. Furthermore, Gata-1 knockdown did not attenuate hmox1a:mCherry fluorescence. However, while there was a complete loss of detection of bvrb expression by ISH at 24 hpf, bvra expression was greatly attenuated but still detectable in Gata-1 morphants. In contrast, 96 hpf Gata-1 morphants displayed increased bvra and bvrb expression within hematopoietic tissues. Finally, temporal expression patterns of enzymes involved in the generation and maintenance of NADPH were consistent with known changes in the cellular redox state during early zebrafish development. Together, these data suggest that Gata-1 and Nrf2a play differential roles in regulating the heme degradation enzymes during an early developmental period of heightened cellular stress.
机译:血红素加氧酶1(HMOX1)将血红素降解为biliverdin,随后通过biliverdin还原酶(BVRa或BVRb)将血红素转化为胆红素,其方式类似于经典的抗氧化剂谷胱甘肽循环途径。为了更好地了解BVR酶在发育过程中可能发挥的潜在抗氧化剂作用,对斑马鱼hmox1a,bvra和bvrb的时空表达和转录调控在基础条件下和对促氧化剂暴露的反应中进行了表征。这三个基因在发育过程中均显示出与经典造血祖细胞一致的时空表达模式。 Nrf2a的瞬时敲低不会减弱通过ISH检测bvra或bvrb的能力,或响应于镉暴露而改变空间表达模式。尽管在中间细胞团中记录了hmox1a:mCherry荧光,但原始红细胞分化的瞬时位置却没有在Nrf2a morphant中完全减弱表达,但实时RT-PCR证明hmox1a表达显着降低。此外,Gata-1组合式不会减弱hmox1a:mCherry荧光。但是,尽管在24 hpf时ISH完全检测不到bvrb表达,但bvra表达大大减弱,但仍可在Gata-1 morphant中检测到。相反,96 hpf Gata-1 morphant显示造血组织内增加的bvra和bvrb表达。最后,参与NADPH产生和维持的酶的时间表达模式与斑马鱼早期发育过程中细胞氧化还原状态的已知变化是一致的。总之,这些数据表明,在细胞应激加剧的早期发育阶段,Gata-1和Nrf2a在调节血红素降解酶中起着不同的作用。

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