Targeting Phospholipase D Pharmacologically Prevents Phagocytic Function Loss of Retinal Pigment Epithelium Cells Exposed to High Glucose Levels

BERMÚDEZ, V (PRIMERA AUTORIA COMPARTIDA); TENCONI, PE (PRIMERA AUTORIA COMPARTIDA); ECHEVARRIA, MS; ASATRIAN, A; CALANDRIA, JM; GIUSTO, NM; BAZAN, N; MATEOS, MV. (CORRESPONDING AUTHOR)

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

MOLECULAR DIVERSITY PRESERVATION INTERNATIONAL-MDPI

Lugar: Basel; Año: 2022

1422-0067

We previously described the participation of canonical phospholipase D isoforms (PLD1and PLD2) in the inflammatory response of retinal pigment epithelium (RPE) cells exposed to highglucose concentrations (HG). Here, we studied the role of the PLD pathway in RPE phagocytic function. For this purpose, ARPE-19 cells were exposed to HG (33 mM) or to normal glucose concentration (NG, 5.5 mM) and phagocytosis was measured using pHrodo™ green bioparticles® or photoreceptor outer segments (POS). HG exposure for 48 and 72 h reduced phagocytic function of ARPE19 cells, and this loss of function was prevented when cells were treated with 5 μM of PLD1(VU0359595 or PLD1i) or PLD2 (VU0285655-1 or PLD2i) selective inhibitors. Furthermore, PLD1iand PLD2i did not affect RPE phagocytosis under physiological conditions and prevented oxidativestress induced by HG. In addition, we demonstrated PLD1 and PLD2 expression in ABC cells, anovel human RPE cell line. Under physiological conditions, PLD1i and PLD2i did not affect ABCcell viability, and partial silencing of both PLDs did not affect ABC cell POS phagocytosis. In conclusion, PLD1i and PLD2i prevent the loss of phagocytic function of RPE cells exposed to HG without affecting RPE function or viability under non-inflammatory conditions.