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腺病毒介导的 Stim1-mKO1 基因转染增加体内大鼠颌下腺腺泡细胞毒蕈碱刺激诱导的 Ca(2+)反应。

Increase in muscarinic stimulation-induced Ca(2+) response by adenovirus-mediated Stim1-mKO1 gene transfer to rat submandibular acinar cells in vivo.

机构信息

Department of Pharmacology, School of Dentistry, Health Sciences University of Hokkaido, Ishikari-Tobetsu, Hokkaido 061-0293, Japan.

出版信息

Biochem Biophys Res Commun. 2013 Oct 4;439(4):433-7. doi: 10.1016/j.bbrc.2013.08.080. Epub 2013 Aug 30.

DOI:10.1016/j.bbrc.2013.08.080
PMID:23998931
Abstract

Adenoviruses have been used for gene transfer to salivary gland cells in vivo. Their use to study the function of salivary acinar cells was limited by a severe inflammatory response and by the destruction of fluid-secreting acinar cells. In the present study, low doses of adenovirus were administered to express Stim1-mKO1 by retrograde ductal injection to submandibular glands. The approach succeeded in increasing muscarinic stimulation-induced Ca(2+) responses in acinar cells without inflammation or decreased salivary secretions. This increased Ca(2+) response was notable upon weak muscarinic stimulation and was attributed to increased Ca(2+) release from internal stores and increased Ca(2+) entry. The basal Ca(2+) level was higher in Stim1-mKO1-expressing cells than in mKO1-expressing and non-expressing cells. Exposure of permeabilized submandibular acinar cells, where Ca(2+) concentration was fixed at 50 nM, to inositol 1,4,5-trisphosphate (IP3) produced similar effects on the release of Ca(2+) from stores in Stim1-mKO1-expressing and non-expressing cells. The low toxicity and relative specificity to acinar cells of the mild gene transfer method described herein are particularly useful for studying the molecular functions of salivary acinar cells in vivo, and may be applied to increase salivary secretions in experimental animals and human in future.

摘要

腺病毒已被用于体内唾液腺细胞的基因转移。它们在研究唾液腺细胞功能方面的应用受到严重炎症反应和分泌液腺泡细胞破坏的限制。在本研究中,通过逆行导管内注射,将低剂量的腺病毒用于表达 Stim1-mKO1,以转染颌下腺。该方法成功地增加了在没有炎症或减少唾液分泌的情况下,刺激剂诱导的腺泡细胞内 Ca(2+)反应。在弱的毒蕈碱刺激下,这种 Ca(2+)反应更为明显,这归因于细胞内储存 Ca(2+)的释放增加和 Ca(2+)内流增加。与 mKO1 表达细胞和非表达细胞相比,表达 Stim1-mKO1 的细胞中的基础 Ca(2+)水平更高。用肌醇 1,4,5-三磷酸(IP3)处理透化的颌下腺泡细胞,将细胞内 Ca(2+)浓度固定在 50 nM,在表达和不表达 Stim1-mKO1 的细胞中,IP3 对细胞内储存 Ca(2+)的释放产生相似的影响。本文所述的温和基因转移方法具有低毒性和相对的腺泡细胞特异性,特别适用于研究体内唾液腺细胞的分子功能,并且将来可能会被应用于增加实验动物和人类的唾液分泌。

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