Comparative transcriptome analysis of endothelial progenitor cells of HbSS patients with and without proliferative retinopathy

Author:

Bertozzo Victor de Haidar e1,da Silva Costa Sueli Matilde1,Ito Mirta Tomie1,Cruz Pedro Rodrigues Sousa da1ORCID,Souza Bruno Batista1,Rios Vinicius Mandolesi1ORCID,Viturino Marina Gonçalves Monteiro2,Castro Júlia Nicoliello Pereira de1,Rodrigues Thiago Adalton Rosa1,Lanaro Carolina3,Albuquerque Dulcinéia Martins de3,Saez Roberta Casagrande3,Olalla Saad Sara Teresinha3,Ozelo Margareth Castro3,Costa Fernando Ferreira3,Melo Mônica Barbosa de1ORCID

Affiliation:

1. Center for Molecular Biology and Genetic Engineering (CBMEG), University of Campinas (UNICAMP), Campinas 13083-875, São Paulo, Brazil

2. Department of Ophthalmology, University of Campinas (UNICAMP), Campinas 13083-887, São Paulo, Brazil

3. Hematology and Hemotherapy Center, University of Campinas (UNICAMP), Campinas 13083-970, São Paulo, Brazil

Abstract

Among sickle cell anemia (SCA) complications, proliferative sickle cell retinopathy (PSCR) is one of the most important, being responsible for visual impairment in 10–20% of affected eyes. The aim of this study was to identify differentially expressed genes (DEGs) present in pathways that may be implicated in the pathophysiology of PSCR from the transcriptome profile analysis of endothelial progenitor cells. RNA-Seq was used to compare gene expression profile of circulating endothelial colony-forming cells (ECFCs) from HbSS patients with and without PSCR. Furthermore, functional enrichment analysis and protein–protein interaction (PPI) networks were performed to gain further insights into biological functions. The differential expression analysis identified 501 DEGs, when comparing the groups with and without PSCR. Furthermore, functional enrichment analysis showed associations of the DEGs in 200 biological processes. Among these, regulation of mitogen-activated protein (MAP) kinase activity, positive regulation of phosphatidylinositol 3-kinase (PI3K), and positive regulation of Signal Transducer and Activator of Transcription (STAT) receptor signaling pathway were observed. These pathways are associated with angiogenesis, cell migration, adhesion, differentiation, and proliferation, important processes involved in PSCR pathophysiology. Moreover, our results showed an over-expression of VEGFC (vascular endothelial growth factor–C) and FLT1 (Fms-Related Receptor Tyrosine Kinase 1) genes, when comparing HbSS patients with and without PSCR. These results may indicate a possible association between VEGFC and FLT1 receptor, which may activate signaling pathways such as PI3K/AKT and MAPK/ERK and contribute to the mechanisms implicated in neovascularization. Thus, our findings contain preliminary results that may guide future studies in the field, since the molecular mechanisms of PSCR are still poorly understood.

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

FAPESP

Publisher

Frontiers Media SA

Subject

General Biochemistry, Genetics and Molecular Biology

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