کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
9436610 | 1615689 | 2005 | 8 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
P2Y2 agonist induces mucin secretion via Ca2+- and inositol 1,4,5-triphosphate-dependent pathway in human middle ear epithelial cells
دانلود مقاله + سفارش ترجمه
دانلود مقاله ISI انگلیسی
رایگان برای ایرانیان
کلمات کلیدی
PLCuridine-5′-triphosphateCa2+ induced Ca2+ releaseUTP2-aminoethoxydiphenyl borate2-APBPKCIP3ERKCa2+ - Ca2 +Inositol 1,4,5-triphosphate - Inositol 1،4،5-تری فسفاتMAPK - MAPK[Ca2+]i - [Ca2 +] iAdenosine Triphosphate - آدنوزین تری فسفاتATP - آدنوزین تری فسفات یا ATPBAPTA-AM - بیایپیتیای-AMdiacylglycerol - دیسیل گلیسیرینDAG - روزextracellular signal regulated kinase - سیگنال خارج سلولی kinase را تنظیم می کندSignaling Transduction - سیگنالینگ انتقالendoplasmic reticulum - شبکه آندوپلاسمی Phospholipase - فسفولیپازMucin - موسین Ca2+ influx - نفوذ Ca2 +Protein kinase C - پروتئین کیناز سیmitogen-activated protein kinase - پروتئین کیناز فعال با mitogenCaffeine - کافئینCICR - کمیته بینالمللی صلیب سرخ
موضوعات مرتبط
علوم زیستی و بیوفناوری
علم عصب شناسی
سیستم های حسی
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
Purinergic agonists regulate mucin secretion in the airway epithelial cells. This study examined the effects of the apical application of purinergic agonists on Ca2+ influx ([Ca2+]i), and mucin secretion along with their underlying signaling pathway in normal human middle ear epithelial (NHMEE) cells. The apical membrane of NHMEE cells were stimulated with various purinergic agonists, including UTP, and the [Ca2+]i was measured using a miniature Ussing double perfusion chamber. P2Y2 receptor in NHMEE cells was also localized by immunohistochemistry. UTP-induced mucin secretion was quantified by an immunoblotting assay. The order of the purinergic agonist potency with respect to [Ca2+]i determined in this study was ATPÂ =Â UTPÂ >Â 2-MeSATPÂ >Â UDPÂ â«Â adenosine which is consistent with that obtained from P2Y2 receptor activation. The P2Y2 receptor is expressed in the apical membrane of monolayered cultured NHMEE cells. Apical UTP-induced [Ca2+]i was inhibited by 2-aminoethoxydiphenyl borate (2-APB) but not by ryanodine. UTP-induced mucin secretion was inhibited by a Ca2+ chelating agent, BAPTA-AM, and was stimulated by ionomycin. UTP-induced mucin secretion was also suppressed by U73122 and 2-APB, while Calphostin C suppressed it to a small extent and PD98059 was ineffective. Caffeine also inhibited the UTP-induced [Ca2+]i and mucin secretion. These results suggest that the P2Y2 receptor is expressed in NHMEE cells, and plays a major role in modulating the [Ca2+]i from the IP3-sensitive intracellular Ca2+ store. UTP-induced mucin secretion in NHMEE cells is strongly dependent on Ca2+- and IP3.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Hearing Research - Volume 209, Issues 1â2, November 2005, Pages 24-31
Journal: Hearing Research - Volume 209, Issues 1â2, November 2005, Pages 24-31
نویسندگان
Jae Young Choi, Ji-Hyun Shin, Jung Lim Kim, Sang Ho Jung, Eun Jin Son, Mee Hyun Song, Sung Huhn Kim, Joo-Heon Yoon,