4.6 Article

Resolvin D1 Increases Mucin Secretion in Cultured Rat Conjunctival Goblet Cells via Multiple Signaling Pathways

期刊

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
卷 58, 期 11, 页码 4530-4544

出版社

ASSOC RESEARCH VISION OPHTHALMOLOGY INC
DOI: 10.1167/iovs.17-21914

关键词

resolvin; goblet cells; secretion; mucins

资金

  1. Norwegian Research Council (Oslo, Norway)
  2. National Institutes of Health (Bethesda, MD, USA) [EY019470, R01GM038765, P30 EY00379035]

向作者/读者索取更多资源

PURPOSE. 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. METHODS. 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. RESULTS. 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 (Ca 2_/CamK). Glycoconjugate secretion was significantly inhibited by PLD, -C, -A2, ERK1/2 and CCa2+/CamK, but not PKC. CONCLUSIONS. 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.

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