课题基金 / 基金详情

MODELS FOR GENETIC DISORDERS

MODELS FOR GENETIC DISORDERS
遗传疾病模型
批准号:
6362995
负责人:
GARY EDWARD SHULL
金额:
$48.73万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1996
资助国家:
美国
项目状态:
已结题
起止时间:
1996-03-01 至 2005-02-28

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中文摘要
翻译
描述(改编自申请人摘要):研究者的
英文摘要
DESCRIPTION (Adapted from the Applicant's Abstract): The investigator's long-term objective is to develop a detailed understanding of the physiological functions of ion transporters involved in secretion and absorption of ions in the gastrointestinal tract and in renal control of acid/base and electrolyte homeostasis. In working toward this goal, they are using gene-targeting technology to examine the in vivo functions of specific transporters. They have already developed null mutant mice for the NHE1,2 and 3 Na/H exchangers, the colonic and gastric H,K-ATPases (cHKA and gHKA), the thiazide-sensitive NaCl cotransporter, and the basolateral NaK2C1 cotransporter (NKCC1). Aim 1 of this proposal is to develop null mutant mice for the NHE4 Na/H exchanger, the AE2 and DRA C1/HCO3 exchangers, the NBC1 Na/HCO3 cotransporter, and the C1C-2 C1 channel, and to perform the initial analyses of their phenotypes. In Aim 2, the transport mechanisms underlying gastric HC1 and KC1 secretion and mucosal protection will be analyzed. These studies will test the hypotheses that C1C-2, AE2, and NHE4 are essential for HC1 secretion by the gastric parietal cell; that NHE2 functions in mucsosa protection and in maintaining parietal cell viability during acid secretion; and that NKCC1 is required for maximum KC1 secretion by gastric glands. In Aim 3, the transport mechanisms underlying absorption and secretion in the intestinal tract will be analyzed. These studies will test the functions of: DRA as the apical C1/HCO3 exchanger mediating C1 absorption; AE2 as the basolateral C1/HCO3 exchanger mediating HCO3 absorption; NHE1 and NKCC1 in toxin-stimulated secretion; NHE2 in blunting the severity of diarrhea states; and cHKA in K recycling in the colon and in providing compensation for diarrhea states. In Aim 4, the function and relative importance of specific transporters in renal function will be analyzed. In these studies they will: analyze the renal phenotypes of mice lacking NKCC1, AE2, and NHE2; test the functions of cHKA and gHKA in HCO3 reabsorption in the collecting duct and in urinary potassium conservation during potassium depletion; and analyze the relative importance of NBC1 and NHE3 in HCO3 reabsorption in the proximal tubule and in acid-base homeostasis. These studies will substantially expand our understanding of the specific functions of individual transporters and how they work together to mediate transepethelial ion transport processes in vivo.
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MODELS FOR GENETIC DISORDERS OF CALCIUM TRANSPORT
  • 批准号:
    2767612
  • 项目类别:
  • 资助金额:
    $42.28万
  • 财政年份:
    1999
  • 负责人:
    GARY EDWARD SHULL
  • 依托单位:
RENAL SODIUM TRANSPORTERS IN CONTROL OF ARTERIAL BLOOD PRESSURE
  • 批准号:
    6202277
  • 项目类别:
  • 资助金额:
    $20.67万
  • 财政年份:
    1999
  • 负责人:
    GARY EDWARD SHULL
  • 依托单位:
MODELS FOR GENETIC DISORDERS OF CALCIUM TRANSPORT
  • 批准号:
    6343645
  • 项目类别:
  • 资助金额:
    $43.55万
  • 财政年份:
    1999
  • 负责人:
    GARY EDWARD SHULL
  • 依托单位:
MODELS FOR GENETIC DISORDERS OF CALCIUM TRANSPORT
  • 批准号:
    6139315
  • 项目类别:
  • 资助金额:
    $43.55万
  • 财政年份:
    1999
  • 负责人:
    GARY EDWARD SHULL
  • 依托单位:
海外基金