Retinoid X receptor activation is essential for docosahexaenoic acid protection of retina photoreceptors

GERMAN, O.L.; MONACO, S.; AGNOLAZZA, D.; ROTSTEIN, N.; POLITI, L.

JLR PAPERS IN PRESS

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC

Lugar: Bethesda, Maryland; Año: 2013 vol. 54 p. 2236 - 2246

0022-2275

We have established that docosahexaenoic acid (DHA), the major polyunsaturated fatty acid in the retina, promotes survival of rat retina photoreceptors during early development in vitro and upon oxidative stress by activating the ERK/MAPK signaling pathway. We now investigated whether DHA turns on this pathway through activation of retinoid X receptors (RXR) or by inducing tyrosine kinase (Trk) receptor activation. We also evaluated whether DHA release from phospholipids was required for its protective effect. Addition of RXR antagonists (HX531, PA452) to rat retinal neuronal cultures inhibited DHA protection during early development in vitro and upon oxidative stress induced with paraquat or H2O2. In contrast, the Trk inhibitor K252a did not affect DHA prevention of photoreceptor apoptosis. These results imply that activation of RXR was required for DHA protection whereas Trk receptors were not involved in this protection. Pretreatment with BEL, a phospholipase A2 inhibitor, blocked DHA prevention of oxidative stress-induced apoptosis of photoreceptors. Noteworthy, RXR agonists (HX630, PA024) also rescued photoreceptors from H2O2-induced apoptosis. These results suggest that DHA is first released from phospholipids and then activates RXR to prevent photoreceptor apoptosis. This is the first evidence in which RXR activation can promote the survival of photoreceptors.