Genetic and immunohistochemical analysis of HSPA5 in mouse and human retinas

• Published in: Molecular vision 2016-11, Vol.22, p.1318-1331
• Main Authors: Chintalapudi, Sumana R, Wang, XiaoFei, Li, Huiling, Lau, Yin H Chan, Williams, Robert W, Jablonski, Monica M
• Format: Article
• Language: English
• Subjects: Aged; Aged, 80 and over; Animals; Computational Biology; Endoplasmic Reticulum Chaperone BiP; Female; Gene Expression Regulation; Genetic Association Studies; Heat-Shock Proteins - genetics; Heat-Shock Proteins - metabolism; Humans; Immunohistochemistry; Male; Mice; Retina - cytology; Retina - metabolism; Sulfatases - genetics; Sulfatases - metabolism; Tissue Donors
• ISSN: 1090-0535

Photoreceptor degenerative diseases are among the leading causes of vision loss. Although the causative genetic mutations are often known, mechanisms leading to photoreceptor degeneration remain poorly defined. We have previously demonstrated that the photoreceptor membrane-associated protein XAP-1 antigen is a product of the gene. In this study, we used systems genetic methods, statistical modeling, and immunostaining to identify and analyze candidate genes that modulate Hspa5 expression in the retina. Quantitative trait locus (QTL) mapping was used to map the genomic region that regulates in the cross between C57BL/6J X DBA/2J mice (BXD) genetic reference panel. The stepwise refinement of candidate genes was based on expression QTL mapping, gene expression correlation analyses (direct and partial), and analysis of regional sequence variants. The subcellular localization of candidate proteins and HSPA5 in mouse and human retinas was evaluated by immunohistochemistry. Differences in the localization of extracellular HSPA5 were assessed between healthy human donor and atrophic age-related macular degeneration (AMD) donor eyes. In the eyes of healthy mice, extracellular HSPA5 was confined to the area around the cone photoreceptor outer segments. Mapping variation in mRNA expression levels in the retina revealed a statistically significant -acting expression QTL (eQTL) on Chromosome 2 (Chr 2) and a suggestive locus on Chr 15. on Chr 2 was the strongest candidate gene based on partial correlation analysis, Pearson correlation with , expression levels in the retina, a missense variant in exon 14, and its reported function in the extracellular matrix and interphotoreceptor matrix. SULF2 is localized to the rod and cone photoreceptors in both human and mouse retinas. In human retinas with no pathology, extracellular HSPA5 was localized around many cones within the macular area. In contrast, fewer HSPA5-immunopositive cones were observed in the retinas from AMD donors. We identified as a candidate gene modulating the expression in the retina. The preferential loss of HSPA5 in the interphotoreceptor matrix around cone photoreceptors in atrophic AMD retinas opens up new avenues for exploring the changes in interphotoreceptor matrix (IPM) that are associated with macular disease.