Suppr超能文献

钙信号缺陷导致唾液腺功能障碍。

Calcium signaling defects underlying salivary gland dysfunction.

机构信息

Secretory Physiology Section, Molecular Physiology and Therapeutics Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA.

出版信息

Biochim Biophys Acta Mol Cell Res. 2018 Nov;1865(11 Pt B):1771-1777. doi: 10.1016/j.bbamcr.2018.07.002. Epub 2018 Jul 10.

Abstract

Salivary glands secrete saliva, a mixture of proteins and fluids, which plays an extremely important role in the maintenance of oral health. Loss of salivary secretion causes a dry mouth condition, xerostomia, which has numerous deleterious consequences including opportunistic infections within the oral cavity, difficulties in eating and swallowing food, and problems with speech. Saliva secretion is regulated by stimulation of specific signaling mechanisms within the acinar cells of the gland. Neurotransmitter-stimulated increase in cytosolic [Ca] ([Ca]) in acinar cells is the primary trigger for salivary fluid secretion from salivary glands, the loss of which is a critical factor underlying dry mouth conditions in patients. The increase in [Ca] regulates multiple ion channel and transport activities that together generate the osmotic gradient which drives fluid secretion across the apical membrane. Ca entry mediated by the Store-Operated Ca Entry (SOCE) mechanism provides the essential [Ca] signals to trigger salivary gland fluid secretion. Under physiological conditions depletion of ER-Ca stores is caused by activation of IP3R by IP3 and this provides the stimulus for SOCE. Core components of SOCE in salivary gland acinar cells are the plasma membrane Ca channels, Orai1 and TRPC1, and STIM1, a Ca-sensor protein in the ER, which regulates both channels. In addition, STIM2 likely enhances the sensitivity of cells to ER-Ca depletion thereby tuning the cellular response to agonist stimulation. Two major, clinically relevant, conditions which cause irreversible salivary gland dysfunction are radiation treatment for head-and-neck cancers and the autoimmune exocrinopathy, Sjögren's syndrome (pSS). However, the exact mechanism(s) that causes the loss of fluid secretion, in either condition, is not clearly understood. A number of recent studies have identified that defects in critical Ca signaling mechanisms underlie salivary gland dysfunction caused by radiation treatment or Sjögren's syndrome (pSS). This chapter will discuss these very interesting and important studies.

摘要

唾液腺分泌唾液,这是一种蛋白质和液体的混合物,在维持口腔健康方面起着极其重要的作用。唾液分泌减少会导致口干,即口腔干燥,这会带来许多有害后果,包括口腔内的机会性感染、进食和吞咽食物的困难以及言语问题。唾液分泌是通过刺激腺体细胞中的特定信号机制来调节的。神经递质刺激细胞内钙([Ca])的增加是唾液腺分泌唾液的主要触发因素,而[Ca]的减少是导致口干患者口干的关键因素。[Ca]的增加调节了多种离子通道和转运活性,这些活性共同产生渗透压梯度,驱动液体穿过顶端膜分泌。由储存操作钙进入(SOCE)机制介导的 Ca 进入提供了触发唾液腺液体分泌的必要[Ca]信号。在生理条件下,内质网-Ca 储存的耗竭是由 IP3 通过 IP3R 激活引起的,这为 SOCE 提供了刺激。唾液腺腺泡细胞中 SOCE 的核心组件是质膜 Ca 通道,Orai1 和 TRPC1,以及内质网中的 Ca 传感器蛋白 STIM1,它调节这两种通道。此外,STIM2 可能增强了细胞对 ER-Ca 耗竭的敏感性,从而调节了细胞对激动剂刺激的反应。导致唾液腺功能不可逆丧失的两种主要的、临床相关的情况是头颈部癌症的放射治疗和自身免疫外分泌疾病,干燥综合征(pSS)。然而,无论是哪种情况,导致液体分泌丧失的确切机制尚不清楚。最近的一些研究已经确定,关键的 Ca 信号机制缺陷是放射治疗或干燥综合征(pSS)引起的唾液腺功能障碍的基础。本章将讨论这些非常有趣和重要的研究。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验