Inhibition of RhoA signaling with increased Bves in trabecular meshwork cells.

Russ PK, Kupperman AI, Presley SH, Haselton FR, Chang MS
Invest Ophthalmol Vis Sci. 2010 51 (1): 223-30

PMID: 19628742 · PMCID: PMC2857412 · DOI:10.1167/iovs.09-3539

PURPOSE - Blood vessel epicardial substance (Bves) is a novel adhesion molecule that regulates tight junction (TJ) formation. TJs also modulate RhoA signaling, which has been implicated in outflow regulation. Given that Bves has been reported in multiple ocular tissues, the authors hypothesize that Bves plays a role in the regulation of RhoA signaling in trabecular meshwork (TM) cells.

METHODS - Human TM cell lines NTM-5 and NTM-5 transfected to overexpress Bves (NTM-w) were evaluated for TJ formation, and levels of occludin, cingulin, and ZO-1 protein were compared. Assays of TJ function were carried out using diffusion of sodium fluorescein and transcellular electrical resistance (TER). Levels of activated RhoA were measured using FRET probes, and phosphorylation of myosin light chain (MLC-p), a downstream target of RhoA, was assessed by Western blot analysis.

RESULTS - Overexpression of Bves led to increased TJ formation in NTM-5 cells. Increased TJ formation was confirmed by increased occludin, cingulin, and ZO-1 protein. Functionally, NTM-w cells showed decreased permeability and increased TER compared with NTM-5 cells, consistent with increased TJ formation. NTM-w cells also exhibited decreased levels of active RhoA and lower levels of MLC-p than did NTM-5 cells. These findings support a TJ role in RhoA signaling.

CONCLUSIONS - Increased Bves in TM cells leads to increased TJ formation with decreased RhoA activation and decreased MLC-p. This is the first report of a regulatory pathway upstream of RhoA in TM cells. In TM tissue, RhoA has been implicated in outflow regulation; thus, Bves may be a key regulatory molecule in aqueous outflow.

MeSH Terms (22)

Avian Proteins Blotting, Western Cell Adhesion Molecules Cell Line Electric Impedance Fluorescein Fluorescent Antibody Technique, Indirect Humans Membrane Proteins Microfilament Proteins Muscle Proteins Myosin Light Chains Occludin Permeability Phosphoproteins Phosphorylation rhoA GTP-Binding Protein Signal Transduction Tight Junctions Trabecular Meshwork Transfection Zonula Occludens-1 Protein

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