کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2430342 1106561 2008 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Phospholipase C, phosphatidylinositol 3-kinase, and intracellular [Ca2+] mediate the activation of chicken HD11 macrophage cells by CpG oligodeoxynucleotide
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شناسی تکاملی
پیش نمایش صفحه اول مقاله
Phospholipase C, phosphatidylinositol 3-kinase, and intracellular [Ca2+] mediate the activation of chicken HD11 macrophage cells by CpG oligodeoxynucleotide
چکیده انگلیسی

SummaryThe activation of phospholipases is one of the earliest key events in receptor-mediated cellular responses to a number of extracellular signaling molecules. Oligodeoxynucleotides containing CpG motifs (CpG ODN) mimic microbial DNA and are immunostimulatory to most vertebrate species. In the present study, we used the production of nitric oxide (NO) as an indicator to evaluate the involvement of the signaling cascades of phospholipases and phosphatidylinositol 3-kinase (PI3K) in the activation of chicken HD11 macrophage cells by CpG ODN. Using selective inhibitors, we have identified the involvement of phosphatidylinositol (PI)-phospholipase C (PI-PLC), but not phosphatidylcholine (PC)-phospholipase C (PC-PLC) and PC-phospholipase D (PC-PLD), in CpG ODN-induced NO production in HD11 cells. Preincubation with PI-PLC selective inhibitors (U-73122) completely abrogated CpG ODN-induced NO production in HD11 cells, whereas PC-PLC inhibitor (D609) and PC-PLD inhibitor (n-butanol) had no inhibitory effects. Additionally, inhibition of PI3K and protein kinase C (PKC) with selective inhibitors and chelation of intracellular [Ca2+] also significantly attenuated NO production in CpG ODN-activated HD11 cells. Our results demonstrate that PI-PLC, PI3 K, PKC, and intracellular [Ca2+] are important components of the CpG ODN-induced signaling pathway that leads to the production of NO in avian macrophage cells.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Developmental & Comparative Immunology - Volume 32, Issue 10, 2008, Pages 1111–1118
نویسندگان
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