Section 81
Chapter 80,276

Molecular and cellular changes induced by the activation of CB2 cannabinoid receptors in trabecular meshwork cells

He, F.; Song, Z.-H.

Molecular Vision 13: 1348-1356


ISSN/ISBN: 1090-0535
PMID: 17679938
Accession: 080275422

To study the role of CB2 cannabinoid receptors in cellular functions of trabecular meshwork (TM) cells including cytoskeleton changes and migration and to investigate the possible signaling pathways utilized by CB2 receptor for these cellular functions. JWH015, a selective CB2 receptor agonist, SR144528, a selective CB2 receptor antagonist, and SR141716A, a selective CB1 receptor antagonist were used on cultured porcine TM cells. In cytoskeleton studies, Alexafluor 488-labeled phalloidin staining was used to examine actin filaments and immunocytochemistry using an anti-paxillin antibody was used to detect focal adhesions on fibronectin-coated glass coverslips. Standard wound-healing assays were used to study cell migration. Rac1-GTP pull-down assays were conducted to examine the changes in the Rac1-GTPase activity. Western-blot analysis with an anti-phospho-cofilin antibody was used to measure the levels of active cofilin. JWH015 (100 nM) significantly inhibited the formation of actin stress fibers and focal adhesions in cultured TM cells. The effect of 100 nM of JWH015 on the cytoskeleton was completely blocked by 1 microM of SR144528 but not by SR141716A. The addition of 100 nM JWH015 decreased the migration of TM cells in wound-healing assays and this effect of JWH015 was blocked by 1 microM of SR144528. In contrast, SR141716A had no effect on the inhibitory effect of JWH015 on TM cell migration. In Rac1-GTP pull-down assays, treatment of TM cells with 100 nM of JWH015 decreased the activity of Rac1 GTPase activity in a time-dependent manner. Pretreatment with 1 microM SR144528, but not with SR141716A, blocked the effect of JWH015 on Rac1 activity. Western blot analysis revealed that JWH015 also diminished the level of phosphorylated cofilin in TM cells and this effect of JWH015 was antagonized by SR144528 but not by SR141716A, indicating a CB2 receptor-mediated activation of cofilin. This study demonstrates that by acting through CB2 receptors, the CB2-selective cannabinoid agonist JWH015 modulates the TM cell actin's cytoskeleton and migration. This study also shows that JWH015 modulates the activities of Rac1-GTPase and cofilin, which are important signaling molecules for the cytoskeletal and migratory properties of TM cells.

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