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DESCRIPTION (provided by applicant): Melanosomes are a specialized organelle of melanocytes that exist in order to conduct a highly specialized task, producing and storing melanin pigment. Melanin acts as a protective agent against the damaging effects of UV radiation. Thus, the presence of melanin in human skin normally contributes to a key element promoting health. Unfortunately, melanosomes are also associated with disease causing potential. Of key concern, many of the intermediates of melanin synthesis are highly reactive quinones and capable of causing significant oxidative damage. Aberrant oxidative stress associated with pigment production has specifically been implicated in several skin diseases, including cutaneous autoimmune disease and malignant melanoma. Despite this importance, the biological processes and ultrastructural components contributing to the ability of melanosomes to contain or detoxify these compounds are largely unknown. Here, we present our preliminary experiments identifying a new melanosomal protein, GPNMB, which we hypothesize participates in the ability of melanosomes to contain or detoxify the potentially cytotoxic intermediates of melanin synthesis. We will test our hypothesis using a combination of genetic epistasis experiments that take advantage of existing Gpnmb mutant mouse strains and synchrotron based imaging techniques that utilize scanning transmission X-ray microscopy. Completion of these experiments will identify a function of the GPNMB protein in melanosomes of the skin, and begin to clarify the role of this protein in health and diseases of pigmentation. Melanosomes are a specialized organelle of melanocytes that in health produce and store melanin pigment and in disease contribute to a variety of skin diseases involving melanocytes. The goal of this research is to initiate functional tests of the newly identified melanosomal protein, GPNMB, utilizing a combination of genetic and innovative imaging approaches. Completion of these studies will yield important gains concerning the melanosomal functions of GPNMB and create needed resources that will facilitate growth of this area of research.
期刊论文(3)
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会议论文
DOI: 10.1111/j.1755-148x.2010.00788.x
发表时间: 2011-02
期刊: Pigment cell & melanoma research
影响因子: 4.3
作者: [Haraszti T, Trantow CM, Hedberg-Buenz A, Grunze M, Anderson MG]
通讯作者: Anderson MG
DOI: 10.1152/ajpregu.00561.2010
发表时间: 2011-06
期刊: American journal of physiology. Regulatory, integrative and comparative physiology
影响因子: --
作者: [H. Stauss;K. Rarick;Katie M Leick;Jason W Burkle;Diane L. Rotella;Michael G. Anderson]
通讯作者: H. Stauss;K. Rarick;Katie M Leick;Jason W Burkle;Diane L. Rotella;Michael G. Anderson
STXMPy: a new software package for automated region of interest selection and statistical analysis of XANES data.
STXMPy:一个新的软件包,用于自动选择感兴趣区域和对 XANES 数据进行统计分析。
DOI: 10.1186/1752-153x-4-11
发表时间: 2010
期刊: Chemistry Central journal
影响因子: --
作者: [Haraszti,Tamás, Grunze,Michael, Anderson,MichaelG]
通讯作者: Anderson,MichaelG
Mechanism of APBB2 contributions to glaucoma
  • 批准号:
    10248474
  • 项目类别:
  • 资助金额:
    $22.48万
  • 财政年份:
    2020
  • 负责人:
    Michael G Anderson
  • 依托单位:
Genetic modifiers of Cep290-mediated retinal degeneration
  • 批准号:
    9759929
  • 项目类别:
  • 资助金额:
    $19.06万
  • 财政年份:
    2018
  • 负责人:
    Michael G Anderson
  • 依托单位:
Rodent Phenotyping Core
  • 批准号:
    10663391
  • 项目类别:
  • 资助金额:
    $17.98万
  • 财政年份:
    2016
  • 负责人:
    Michael G Anderson
  • 依托单位:
Rodent Phenotyping Core
  • 批准号:
    10488232
  • 项目类别:
  • 资助金额:
    $17.98万
  • 财政年份:
    2016
  • 负责人:
    Michael G Anderson
  • 依托单位:
国内基金
海外基金
层出镰刀菌氮代谢调控因子AreA 介导伏马菌素 FB1 生物合成的作用机理
  • 批准号:
    2021JJ40433
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2021
  • 负责人:
    孙磊
  • 依托单位:
寄主诱导梢腐病菌AreA和CYP51基因沉默增强甘蔗抗病性机制解析
  • 批准号:
    32001603
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    24.0万元
  • 批准年份:
    2020
  • 负责人:
    段真珍
  • 依托单位:
AREA国际经济模型的移植.改进和应用
  • 批准号:
    18870435
  • 项目类别:
    面上项目
  • 资助金额:
    2.0万元
  • 批准年份:
    1988
  • 负责人:
    史树中
  • 依托单位: