Please use this identifier to cite or link to this item:
|標題:||Calcium homeostasis and its relationship to superoxide production in blood and milk neutrophils of lactating goats||作者:||Chiang, C.C.
|關鍵字:||PMN;Ca(2+) homeostasis;O(2-) production;Goat;Milk;Blood;escherichia-coli mastitis;protein-kinase-c;respiratory burst;dairy-cows;bovine neutrophils;mammary-gland;nadph oxidase;phorbol;ester;activation;chemiluminescence||Project:||Veterinary Immunology and Immunopathology||期刊/報告no：:||Veterinary Immunology and Immunopathology, Volume 133, Issue 2-4, Page(s) 125-132.||摘要:||
Polymorphonuclear neutrophils (PMN), which comprise over 70% of the somatic cells in goat milk, are a major cellular component of innate immunity in the goat mammary gland. However, the function of milk PMNs is modified after diapedesis compared to PMNs in blood. As many aspects of PMN activity depend directly on intracellular Ca(2+) concentration ((Ca(2+))(i)), the present study aimed to determine the changes in Ca(2+) homeostasis of milk PMNs from lactating goats compared to autologous blood PMNs, and to examine the significance of these variations to the immuno-competency of milk PMNs. The intracellular Ca(2+) store of freshly prepared milk cells was estimated from the elevation of (Ca(2+))(i) after ionomycin treatment, which was found to be significantly less than blood PMNs. Replenishment of the intracellular Ca(2+) store in milk cells after intracellular Ca(2+) depletion by Bapta-AM followed by spiking with 2.5 mM Ca(2+) for 20 min was also compared to that of blood PMNs, showing that after depletion/spiking the intracellular Ca2+ store in milk cells was much less than blood PMNs. The production of superoxide anion (O(2)(-)) in vitro in response to (Ca(2+))(i)-dependent or (Ca(2+))(i)-independent modulators was used to evaluate the relevance of altered Ca(2+) homeostasis on the immunocompetency of milk cells compared to blood PMNs. The results indicated that milk cells produced similarly low levels Of O(2)(-) as blood PMNs when treated with ionomycin. However, the amount Of O(2)(-) produced by milk cells in response to phorbol 12-myristate 13-acetate (PMA) stimulation, although greater than ionomycin treatment, was significantly less than that of blood, PMNs. The capacity for O(2)(-) production by both cell types in response to PMA reverted to the resting state with use of the protein kinase C (PKC) inhibitor, staurosporine. In conclusion, the current study demonstrated an irreversible shortage of intracellular Ca(2+) in the milk PMNs of lactating goats compared to blood PMNs. It also showed that preliminary O(2)(-) production, primed by ionomycin treatment, remained unchanged in milk PMNs, despite the shortage in intracellular Ca(2+), but decreased O(2)(-) production capacity, mediated via the PKC pathway, in milk PMN. It is suggested that the defects in Ca(2+) homeostasis in milk PMNs of lactating goats is partially attributable for the post-diapedesis functionality modifications. (C) 2009 Elsevier B.V. All rights reserved.
|Appears in Collections:||動物科學系|
Show full item record
TAIR Related Article
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.