Lippestad Marit, Hodges Robin R, Utheim Tor P, Serhan Charles N, Dartt Darlene A
Schepens Eye Research Institute, Massachusetts Eye and Ear Infirmary, Department of Ophthalmology, Harvard Medical School, Boston, Massachusetts, United States.
Faculty of Medicine, University of Oslo, Oslo, Norway.
Invest Ophthalmol Vis Sci. 2017 Sep 1;58(11):4530-4544. doi: 10.1167/iovs.17-21914.
Goblet cells in the conjunctiva secrete mucin into the tear film protecting the ocular surface. The proresolution mediator resolvin D1 (RvD1) regulates mucin secretion to maintain homeostasis during physiological conditions and in addition, actively terminates inflammation. We determined the signaling mechanisms used by RvD1 in cultured rat conjunctival goblet cells to increase intracellular [Ca2+] ([Ca2+]i) and induce glycoconjugate secretion.
Increase in [Ca2+]i were measured using fura 2/AM and glycoconjugate secretion determined using an enzyme-linked lectin assay with the lectin Ulex Europaeus Agglutinin 1. Signaling pathways activated by RvD1 were studied after goblet cells were pretreated with signaling pathway inhibitors before stimulation with RvD1. The results were compared with results when goblet cells were stimulated with RvD1 alone and percent inhibition calculated.
The increase in [Ca2+]i stimulated by RvD1 was blocked by inhibitors to phospholipases (PL-) -D, -C, -A2, protein kinase C (PKC), extracellular signal-regulated kinases (ERK)1/2 and Ca2+/calmodulin-dependent kinase (Ca2+/CamK). Glycoconjugate secretion was significantly inhibited by PLD, -C, -A2, ERK1/2 and Ca2+/CamK, but not PKC.
We conclude that RvD1 increases glycoconjugate secretion from goblet cells via multiple signaling pathways including PLC, PLD, and PLA2, as well as their signaling components ERK1/2 and Ca2+/CamK to preserve the mucous layer and maintain homeostasis by protecting the eye from desiccating stress, allergens, and pathogens.
结膜中的杯状细胞向泪膜分泌黏蛋白,以保护眼表。促消退介质消退素D1(RvD1)在生理条件下调节黏蛋白分泌以维持体内平衡,此外,还能积极终止炎症。我们确定了RvD1在培养的大鼠结膜杯状细胞中用于增加细胞内钙离子浓度([Ca2+]i)并诱导糖缀合物分泌的信号传导机制。
使用fura 2/AM测量[Ca2+]i的增加,并使用伴刀豆凝集素1(Ulex Europaeus Agglutinin 1)通过酶联凝集素测定法确定糖缀合物分泌。在用RvD1刺激之前,先用信号通路抑制剂预处理杯状细胞,研究RvD1激活的信号通路。将结果与仅用RvD1刺激杯状细胞时的结果进行比较,并计算抑制百分比。
RvD1刺激引起的[Ca2+]i增加被磷脂酶(PL)-D、-C、-A2、蛋白激酶C(PKC)、细胞外信号调节激酶(ERK)1/2和钙/钙调蛋白依赖性激酶(Ca2+/CamK)的抑制剂所阻断。糖缀合物分泌受到PLD,-C,-A2,ERK1/2和Ca2+/CamK的显著抑制,但不受PKC的抑制。
我们得出结论,RvD1通过多种信号通路增加杯状细胞的糖缀合物分泌,这些信号通路包括PLC、PLD和PLA2,以及它们的信号成分ERK1/2和Ca2+/CamK,以保护眼睛免受干燥应激、过敏原和病原体的侵害,从而维持黏液层并保持体内平衡。