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Development of the mature zebrafish as an animal model of human disease and aging.

机译:开发成熟的斑马鱼作为人类疾病和衰老的动物模型。

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摘要

Zebrafish are a valuable model for developmental biology. However, mature zebrafish biology has not been explored, although many attributes suggest it will also be an important model for study of aging. This dissertation characterizes basic physiologic features and defines mechanisms of stress response of mature zebrafish. The hematological and biochemical parameters of mature zebrafish, including leukocyte differentials, total erythrocyte counts, and serum biochemical analytes, were within range of reported values for other fish species. These results provide reference values to compare with mutated zebrafish.; To further develop zebrafish as models for human disease and aging, I characterized the heat shock response of zebrafish. Heat shock proteins (Hsps) are involved in many physiological processes and are diminished with age in other species. Accordingly, mature zebrafish were exposed to heat stress and various tissues analyzed for Hsp expression. Hsp70 and Hsp47 were upregulated in a tissue-specific manner, while Hsp90alpha, Hsp90beta, and Hsf1a were expressed but not upregulated in response to heat stress. A comparison of young versus mature zebrafish revealed decreased basal levels of Hsp70 and increased levels of Hsf1a in mature fish, demonstrating that there are age differences in their heat shock response, which supports use of mature zebrafish for study of heat shock response and aging.; To further define the mechanism of heat shock response in zebrafish, I explored if heat stress-induces Hsp70 expression through ERK activation, as has been reported for mammals. Heat stress induced both Hsp70 expression and ERK1/2 phosphorylation in zebrafish Pac2 cells. Although ERK inhibitors PD98059 and U0126 blocked ERK1/2 phosphorylation, they did not block heat stress-induced Hsp70 expression. These results demonstrate that heat stress induces Hsp70 expression independent of ERK activation in Pac2 cells. This observation suggests that the heat shock response in zebrafish utilizes a different signaling pathway from that of mammals.; In conclusion, these results characterize aspects of normal physiology and age-related changes in zebrafish. Furthermore, they suggest that the mechanism through which zebrafish promotes a heat stress response is different from mammals. Taken together, these data support the role for mature zebrafish in comparative studies of aging.
机译:斑马鱼是发育生物学的宝贵模型。然而,尽管许多特性表明它也将是研究衰老的重要模型,但尚未探索成熟的斑马鱼生物学。本文表征了基本的生理特征,并确定了成熟斑马鱼的应激反应机制。成熟斑马鱼的血液学和生化参数,包括白细胞差异,总红细胞数和血清生化分析物,均在其他鱼类报告值范围内。这些结果提供了与突变斑马鱼进行比较的参考值。为了进一步发展斑马鱼作为人类疾病和衰老的模型,我对斑马鱼的热激反应进行了表征。热休克蛋白(Hsps)参与许多生理过程,并且在其他物种中随着年龄的增长而降低。因此,成熟的斑马鱼暴露于热应激下,分析了各种组织的Hsp表达。 Hsp70和Hsp47以组织特异性的方式上调,而Hsp90alpha,Hsp90beta和Hsf1a则表达但不上调,以响应热应激。幼龄斑马鱼与成熟斑马鱼的比较显示,成熟鱼的基础Hsp70水平降低而Hsf1a水平升高,表明它们的热休克反应存在年龄差异,这支持使用成熟斑马鱼研究热休克反应和衰老。为了进一步定义斑马鱼中热休克反应的机制,我探讨了热应激是否通过ERK激活诱导Hsp70表达,如哺乳动物的报道。热应激诱导斑马鱼Pac2细胞中的Hsp70表达和ERK1 / 2磷酸化。尽管ERK抑制剂PD98059和U0126阻止ERK1 / 2磷酸化,但它们并未阻止热应激诱导的Hsp70表达。这些结果表明,热应激诱导了Hsp70表达,而与Pac2细胞中的ERK活化无关。该观察结果表明,斑马鱼的热休克反应利用了与哺乳动物不同的信号传导途径。总之,这些结果表征了斑马鱼的正常生理和与年龄相关的变化。此外,他们认为斑马鱼促进热应激反应的机制与哺乳动物不同。综上所述,这些数据支持成熟斑马鱼在衰老比较研究中的作用。

著录项

  • 作者

    Murtha, Jill Marie.;

  • 作者单位

    University of Michigan.;

  • 授予单位 University of Michigan.;
  • 学科 Health Sciences Pathology.
  • 学位 Ph.D.
  • 年度 2003
  • 页码 116 p.
  • 总页数 116
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 病理学;
  • 关键词

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