| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4011824 | Experimental Eye Research | 2010 | 10 Pages |
Best’s vitelliforme macular degeneration is an inherited retinal degeneration associated with a reduction of the light-peak in the patient’s electro-oculogram. Bestrophin-1, the product of the disease-promoting/forming gene can function as regulator of voltage-dependent L-type Ca2+ channels in the retinal pigment epithelium (RPE). Since mice deficient for either β4-subunits or CaV1.3 subunits show reduced light-peaks, the regulatory function of bestrophin-1 on heterologously expressed Ca2+ channels composed of the pore-forming CaV1.3 and the auxiliary β4-subunit was analyzed. Precipitation of β4-subunits led to co-precipitation with bestrophin-1 and subsequent analysis of subcellular localization showed co-localization of bestrophin-1, CaV1.3 and β4-subunit in the cell membrane. CaV1.3 currents in the presence of β4-subunits and bestrophin-1 showed accelerated time-dependent activation and decreased current density compared to currents measured in the absence of bestrophin-1. In the presence of the β3-subunit, which is not expressed in the RPE bestrophin-1 did not modulate CaV1.3 activity. Deletion of a cluster of proline-rich motifs in the C-terminus of bestrophin-1 reduced its co-immuno precipitation with the β4-subunit and strongly reduced the CaV1.3 activity. Cells co-expressing bestrophin-1 lacking the proline-rich motifs and CaV1.3 subunits showed less efficient trafficking of bestrophin-1 into the cell membrane. In summary, we conclude that bestrophin-1 modulates L-type channels of the RPE via proline-rich motif-dependent interaction with β4-subunits. A disturbed interaction reduces the currents of the CaV1.3 subunits. This mechanism could open new ways to understand changes in the patient’s electro-oculogram and functional alterations of the RPE leading to retinal degeneration.
Graphical abstractFigure optionsDownload full-size imageDownload high-quality image (69 K)Download as PowerPoint slideResearch highlights►Bestrophin-1 and L-type Ca2+ channel Cav1.3 co-localize in the basolateral membrane of the retinal pigment epithelium. ►Bestrophin-1 modulates Cav1.3 channel currents. ►Regulation of Cav1.3 channels occurs via direct binding to Ca2+ channel β4-subunits.
