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DESCRIPTION: The quality of life for millions of Americans is adversely affected by salivary gland hypofunction caused by a variety of etiologies including systemic diseases, radiation therapy, xerogenic medications, and Sj6gren's syndrome. The development of interventions to restore function for these individuals requires a thorough understanding of the molecular physiology of salivary glands. Salivary secretion involves a two-step process: acinar cells initially secrete an isotonic, plasma-like fluid; duct cells subsequently modify this primary secretion to conserve NaC1. Both the fluid secretion and NaC1 reabsorption processes are dependent upon the coordinated action of multiple Na+ transport mechanisms including Na+/H+ exchangers, Na+ channels, and Na+/K+/2C1- co-transporters. Genetically modified mice have proven to be valuable models of human salivary gland dysfunction, and are useful for confirming the molecular identities and the functional properties of important Na+ transporters. Nevertheless, significant gaps remain in our understanding of the function of the major Na+ transporting proteins. To address remaining questions, we propose a molecular and functional comparison of Na+ transporter physiology in human and mouse salivary glands. We will test the overall hypothesis that Na+ transport proteins are critical to saliva formation. Specifically: Aim 1) will take advantage of genetically modified mice generated by targeted disruption of the Na+ channel ENaC (Scrmla) and the Na+/H+ exchanger Nhe4 [Slc9a4) genes to directly test whether these Na+ transport proteins are essential for salivary gland secretion; Aim 2) will assess whether agonists that mobilize intracellular Ca 2+, or increase the intracellular cAMP content, acutely regulate the activity of the different Na+ transport mechanisms in human and mouse salivary cells; and Aim 8) will determine whether gene disruption affects saliva production through systemic or gland-specific mechanisms. Ultimately, the information gained from these Aims will aid in the development of therapies to remedy various forms of salivary gland dysfunction.
期刊论文(42)
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Cl- fluxes related to fluid secretion by the rat parotid: involvement of Cl(-)-HCO3- exchange.
Cl- 通量与大鼠腮腺液体分泌相关:Cl(-)-HCO3- 交换的参与。
DOI: 10.1152/ajpgi.1992.262.3.g393
发表时间: 1992
期刊: The American journal of physiology
影响因子: --
作者: [Melvin,JE, Turner,RJ]
通讯作者: Turner,RJ
Expression of multiple Na+/H+ exchanger isoforms in rat parotid acinar and ductal cells.
大鼠腮腺腺泡和导管细胞中多种 Na /H 交换异构体的表达。
DOI: 10.1152/ajpgi.1999.276.2.g470
发表时间: 1999
期刊: The American journal of physiology
影响因子: --
作者: [Park,K, Olschowka,JA, Richardson,LA, Bookstein,C, Chang,EB, Melvin,JE]
通讯作者: Melvin,JE
Secretagogue-induced mobilization of an intracellular Mg2+ pool in rat sublingual mucous acini.
促分泌剂诱导大鼠舌下粘液腺泡细胞内 Mg2 池的动员。
DOI: --
发表时间: 1992
期刊: The Journal of biological chemistry
影响因子: --
作者: [Zhang,GH, Melvin,JE]
通讯作者: Melvin,JE
DOI: 10.1016/j.scr.2012.01.002
发表时间: 2012-05
期刊: STEM CELL RESEARCH
影响因子: 1.2
作者: [Rugel-Stahl, Anastasia, Elliott, Marilyn E., Ovitt, Catherine E.]
通讯作者: Ovitt, Catherine E.
19
    Cellular plasticity in salivary gland regeneration.
    • 批准号:
      10209154
    • 项目类别:
    • 资助金额:
      $45.14万
    • 财政年份:
      2021
    • 负责人:
      Catherine Ovitt
    • 依托单位:
    Single chemosensory cells in the salivary gland.
    • 批准号:
      9757746
    • 项目类别:
    • 资助金额:
      $19.62万
    • 财政年份:
      2018
    • 负责人:
      Catherine Ovitt
    • 依托单位:
    Cell Based Regeneration of Salivary Glands
    • 批准号:
      8517643
    • 项目类别:
    • 资助金额:
      $37.08万
    • 财政年份:
      2012
    • 负责人:
      Catherine Ovitt
    • 依托单位:
    Cell Based Regeneration of Salivary Glands
    • 批准号:
      8685769
    • 项目类别:
    • 资助金额:
      $38.63万
    • 财政年份:
      2012
    • 负责人:
      Catherine Ovitt
    • 依托单位:
    海外基金