Title | Retinal Pigment Epithelium-Secreted VEGF-A Induces Alpha-2-Macroglobulin Expression in Endothelial Cells. |
Publication Type | Journal Article |
Year of Publication | 2022 |
Authors | Lehmann GL, Ginsberg M, Nolan DJ, Rodríguez C, Martínez-González J, Zeng S, Voigt AP, Mullins RF, Rafii S, Rodriguez-Boulan E, Benedicto I |
Journal | Cells |
Volume | 11 |
Issue | 19 |
Date Published | 2022 Sep 24 |
ISSN | 2073-4409 |
Keywords | Antibodies, Blocking, Culture Media, Conditioned, Endothelial Cells, Female, Gelatinases, Humans, Matrix Metalloproteinase 2, Pregnancy, Pregnancy-Associated alpha 2-Macroglobulins, Protease Inhibitors, Recombinant Proteins, Retinal Pigment Epithelium, Transcription Factors, Vascular Endothelial Growth Factor A |
Abstract | <p>Alpha-2-macroglobulin (A2M) is a protease inhibitor that regulates extracellular matrix (ECM) stability and turnover. Here, we show that A2M is expressed by endothelial cells (ECs) from human eye choroid. We demonstrate that retinal pigment epithelium (RPE)-conditioned medium induces A2M expression specifically in ECs. Experiments using chemical inhibitors, blocking antibodies, and recombinant proteins revealed a key role of VEGF-A in RPE-mediated A2M induction in ECs. Furthermore, incubation of ECs with RPE-conditioned medium reduces matrix metalloproteinase-2 gelatinase activity of culture supernatants, which is partially restored after A2M knockdown in ECs. We propose that dysfunctional RPE or choroidal blood vessels, as observed in retinal diseases such as age-related macular degeneration, may disrupt the crosstalk mechanism we describe here leading to alterations in the homeostasis of choroidal ECM, Bruch's membrane and visual function.</p> |
DOI | 10.3390/cells11192975 |
Alternate Journal | Cells |
PubMed ID | 36230937 |
PubMed Central ID | PMC9564307 |
Grant List | R01 EY008538 / EY / NEI NIH HHS / United States R01 EY024605 / EY / NEI NIH HHS / United States R01 GM034107 / GM / NIGMS NIH HHS / United States T32 GM139776 / GM / NIGMS NIH HHS / United States |