Suppr超能文献

干燥综合征NOD.B10小鼠模型下颌下腺细胞中P2Y2核苷酸受体上调

P2Y2 nucleotide receptor up-regulation in submandibular gland cells from the NOD.B10 mouse model of Sjögren's syndrome.

作者信息

Schrader Ann M, Camden Jean M, Weisman Gary A

机构信息

Department of Medical Pharmacology and Physiology, University of Missouri-Columbia, Columbia, MO 65211, USA.

出版信息

Arch Oral Biol. 2005 Jun;50(6):533-40. doi: 10.1016/j.archoralbio.2004.11.005. Epub 2004 Dec 15.

Abstract

UNLABELLED

Sjögren's syndrome (SS) is an autoimmune disease that specifically targets exocrine glands, including salivary glands, and results in an impairment of secretory function. P2Y(2) nucleotide receptors for extracellular ATP and UTP are up-regulated in response to stress or injury in a variety of tissues including submandibular glands (SMGs) [Ahn JS, Camden JM, Schrader AM, Redman RS, Turner JT. Reversible regulation of P2Y(2) nucleotide receptor expression in the duct-ligated rat submandibular gland. Am J Physiol Cell Physiol 2000;279:C286-94; Hou M, Malmsjö M, Möller S, Pantev E, Bergdahl A, Zhai X-H, et al. Increase in cardiac P2X(1)- and P2Y(2)-receptor mRNA levels in congestive heart failure. Life Sci 1999;65:1195-206; Kishore BK, Wang Z, Rab H, Haq M, Soleimani M. Upregulation of P2Y(2) purinoceptor during ischemic reperfusion injury (IRI): possible relevance to diuresis of IRI. J Am Soc Nephrol 1998;9:581 (abstract); Koshiba M, Apasov S, Sverdlov V, Chen P, Erb L, Turner JT, et al. Transient up-regulation of P2Y(2) nucleotide receptor mRNA expression is an immediate early gene response in activated thymocytes. Proc Natl Acad Sci U S A 1997;94:831-6; Turner JT, Landon LA, Gibbons SJ, Talamo BR. Salivary gland P2 nucleotide receptors. Crit Rev Oral Biol Med 1999;10:210-24; Seye CI, Gadeau AP, Daret D, Dupuch F, Alzieu P, Capron L, et al. Overexpression of the P2Y(2) purinoceptor in intimal lesions of the rat aorta. Arterioscler Thromb Vasc Biol 1997;17:3602-10; Seye C, Kong Q, Erb L, Garrad RC, Krugh B, Wang M, et al. Functional P2Y(2) nucleotide receptors mediate uridine 5'-triphosphate-induced intimal hyperplasia in collared rabbit carotid arteries. Circulation 2002;106:2720-6].

OBJECTIVE

To assess whether P2Y(2) receptor expression is up-regulated in SMGs of the NOD.B10 mouse model of primary SS as compared to SMGs of normal C57BL/6 mice.

DESIGN

SMG cells were isolated from normal C57BL/6 and diseased NOD.B10 mice. P2Y(2) receptor mRNA expression was determined by reverse transcription-polymerase chain reaction (RT-PCR) and in situ hybridization, whereas functional P2Y(2) receptor activity was analyzed by measuring UTP-induced increases in Ca(2+).

RESULTS

In contrast to SMG cells from C57BL/6 mice, SMG cells from 4- to 19-week-old NOD.B10 mice exhibited increased P2Y(2) receptor mRNA localized to both ductal and acinar cell types. The levels of mRNA for other uridine nucleotide receptors, i.e., P2Y(4) and P2Y(6) receptors, showed no significant differences between SMG cells of C57BL/6 and NOD.B10 mice, suggesting that only the P2Y(2) receptor was up-regulated in NOD.B10 mice. Moreover, P2Y(2) receptor activity in SMG cells from NOD.B10 mice increased with age (i.e., disease progression).

CONCLUSION

P2Y(2) receptor up-regulation in SMGs is associated with the SS phenotype in NOD.B10 mice, which encourages further attempts to determine the role of this pathway in the development of SS.

摘要

未标记

干燥综合征(SS)是一种自身免疫性疾病,专门针对包括唾液腺在内的外分泌腺,导致分泌功能受损。细胞外ATP和UTP的P2Y(2)核苷酸受体在包括下颌下腺(SMG)在内的多种组织中,响应应激或损伤而上调[Ahn JS, Camden JM, Schrader AM, Redman RS, Turner JT. 导管结扎大鼠下颌下腺中P2Y(2)核苷酸受体表达的可逆调节。美国生理学杂志:细胞生理学2000;279:C286 - 94; Hou M, Malmsjö M, Möller S, Pantev E, Bergdahl A, Zhai X - H, 等。充血性心力衰竭时心脏P2X(1)和P2Y(2)受体mRNA水平的增加。生命科学1999;65:1195 - 206; Kishore BK, Wang Z, Rab H, Haq M, Soleimani M. 缺血再灌注损伤(IRI)期间P2Y(2)嘌呤受体的上调:与IRI利尿的可能相关性。美国肾脏病学会杂志1998;9:581(摘要); Koshiba M, Apasov S, Sverdlov V, Chen P, Erb L, Turner JT, 等。P2Y(2)核苷酸受体mRNA表达的瞬时上调是活化胸腺细胞中的即时早期基因反应。美国国家科学院院刊1997;94:831 - 6; Turner JT, Landon LA, Gibbons SJ, Talamo BR. 唾液腺P2核苷酸受体。口腔生物学与医学评论1999;10:210 - 24; Seye CI, Gadeau AP, Daret D, Dupuch F, Alzieu P, Capron L, 等。大鼠主动脉内膜病变中P2Y(2)嘌呤受体的过度表达。动脉硬化、血栓形成和血管生物学1997;17:3602 - 10; Seye C, Kong Q, Erb L, Garrad RC, Krugh B, Wang M, 等。功能性P2Y(2)核苷酸受体介导尿苷5'-三磷酸诱导的带环兔颈动脉内膜增生。循环2002;106:2720 - 6]。

目的

评估与正常C57BL/6小鼠的下颌下腺相比,原发性干燥综合征NOD.B10小鼠模型的下颌下腺中P2Y(2)受体表达是否上调。

设计

从正常C57BL/6和患病的NOD.B10小鼠中分离下颌下腺细胞。通过逆转录 - 聚合酶链反应(RT - PCR)和原位杂交测定P2Y(2)受体mRNA表达,而通过测量UTP诱导的细胞内钙离子浓度([Ca(2 +)]i)增加来分析功能性P2Y(2)受体活性。

结果

与C57BL/6小鼠的下颌下腺细胞相比,4至19周龄NOD.B10小鼠的下颌下腺细胞显示P2Y(2)受体mRNA增加,定位于导管和腺泡细胞类型。其他尿苷核苷酸受体,即P2Y(4)和P2Y(6)受体的mRNA水平在C57BL/6和NOD.B10小鼠的下颌下腺细胞之间没有显著差异,表明在NOD.B10小鼠中只有P2Y(2)受体上调。此外,NOD.B10小鼠下颌下腺细胞中的P2Y(2)受体活性随年龄(即疾病进展)增加。

结论

NOD.B10小鼠下颌下腺中P2Y(2)受体上调与干燥综合征表型相关,这鼓励进一步尝试确定该途径在干燥综合征发展中的作用。

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