HOMEPRODUCTSSERVICESCOMPANYCONTACTFAQResearchDictionaryPharmaMobileSign Up FREE or Login

Expression of functional leukotriene B4 receptors on human airway smooth muscle cells.

AbstractBACKGROUND:
Leukotriene B4 (LTB4) increases in induced sputum and exhaled breath condensate in people with asthma. Furthermore, the T(H)2-type immune response and airway hyperresponsiveness induced by ovalbumin sensitization is markedly suppressed in LTB4 receptor (BLT) 1 null mice. These studies suggest that LTB4 may contribute to asthma pathophysiology. However, the direct effects of LTB4 on human airway smooth muscle (ASM) have not been studied.
OBJECTIVES:
We sought to determine the expression of LTB4 receptors on human ASM and its functional role in mediating responses of human ASM cells, and the effect of LTB4 on these cells.
METHODS:
Immunohistochemistry, RT-PCR, Western blotting, and flow cytometry were used to determine the expression of LTB4 receptors. To determine the effect of LTB4 on human ASM cells, cell proliferation was assessed by counting cells, and chemokinesis was assessed by gold particle phagokinesis assay.
RESULTS:
We confirmed expression of both BLT1 and BLT2 in human ASM cells in bronchial tissue and in cell culture. LTB4 markedly induced cyclin D1 expression, proliferation, and chemokinesis of human ASM cells. LTB4 also induced phosphorylation of both p42/p44 mitogen-activated protein kinase (MAPK) and downstream PI3 kinase effector, Akt1. However, we observed no induction of c-Jun N-terminal kinase or p38 MAPK. Notably, LTB4-induced migration and proliferation of ASM cells were inhibited by the BLT1 specific antagonist, U75302, and by inhibitors of p42/p44 MAPK phosphorylation (U1026), and PI3 kinase (LY294002).
CONCLUSIONS:
These observations are the first to suggest a role for a LTB4-BLT1 signaling axis in ASM responses that may contribute to the pathogenesis of airway remodeling in asthma.
AuthorsSatoko Watanabe, Akira Yamasaki, Kiyoshi Hashimoto, Yasushi Shigeoka, Hiroki Chikumi, Yasuyuki Hasegawa, Takashi Sumikawa, Miyako Takata, Ryota Okazaki, Masanari Watanabe, Tsuyoshi Yokogawa, Miki Yamamura, Tatsuya Hayabuchi, William T Gerthoffer, Andrew J Halayko, Eiji Shimizu
JournalThe Journal of allergy and clinical immunology (J Allergy Clin Immunol) Vol. 124 Issue 1 Pg. 59-65.e1-3 (Jul 2009) ISSN: 1097-6825 [Electronic] United States
PMID19477492 (Publication Type: Journal Article)
Chemical References
  • LTB4R protein, human
  • RNA, Messenger
  • Receptors, Leukotriene B4
  • Cyclin-Dependent Kinases
  • cyclin-dependent kinase-activating kinase
  • Mitogen-Activated Protein Kinase 3
Topics
  • Blotting, Western
  • Bronchi (immunology, metabolism)
  • Cell Line
  • Cell Movement
  • Cell Proliferation
  • Cyclin-Dependent Kinases (metabolism)
  • Gene Expression Regulation
  • Humans
  • Immunohistochemistry
  • Mitogen-Activated Protein Kinase 3 (metabolism)
  • Myocytes, Smooth Muscle (immunology, metabolism)
  • Phosphorylation
  • RNA, Messenger (metabolism)
  • Receptors, Leukotriene B4 (genetics, metabolism)
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research network!


Choose Username:
Email:
Password:
Verify Password: