Control of lens development by Lhx2-regulated neuroretinal FGFs

Author:

Thein Thuzar1,de Melo Jimmy1,Zibetti Cristina1,Clark Brian S.1,Juarez Felicia1,Blackshaw Seth12345ORCID

Affiliation:

1. Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, 733 N. Broadway, Baltimore, MD, USA

2. Department of Ophthalmology, Johns Hopkins University School of Medicine, 733 N. Broadway, Baltimore, MD, USA

3. Department of Neurology, Johns Hopkins University School of Medicine, 733 N. Broadway, Baltimore, MD, USA

4. Center for Human Systems Biology, Johns Hopkins University School of Medicine, 733 N. Broadway, Baltimore, MD, USA

5. Institute for Cell Engineering, Johns Hopkins University School of Medicine, 733 N. Broadway, Baltimore, MD, USA

Abstract

Fibroblast growth factor (FGF) signaling is an essential regulator of lens epithelial cell proliferation and survival, as well as lens fiber cell differentiation. However, the identities of these FGF factors, their source tissue, and the genes that regulate their synthesis are unknown. We have found that Chx10-Cre;Lhx2lox/lox mice, which selectively lack Lhx2 expression in neuroretina from E10.5, showed an early arrest in lens fiber development along with severe microphthalmia. These mutant animals showed reduced expression of multiple neuroretina-expressed FGFs and canonical FGF-regulated genes in neuroretina. When FGF expression was genetically restored in Lhx2-deficient neuroretina of Chx10-Cre;Lhx2lox/lox mice, we observed a partial but nonetheless substantial rescue of the defects in lens cell proliferation, survival and fiber differentiation. These data demonstrate that neuroretinal expression of Lhx2 and neuroretina-derived FGF factors are crucial for lens fiber development in vivo.

Funder

Office of Extramural Research, National Institutes of Health

Knights Templar Eye Foundation

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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