UK Biology Research May Lead to Treatment for Blinding Disorders, Including Glaucoma

If you, like us at ZeClinics, are into ophthalmology, then Jakub Famulski from the University of Kentucky and his state-of- the-art zebrafish work might just... catch your eye.

We at ZeClinics know a thing or two about the value of zebrafish in the study of vision-related disorders such as AMD or ASD: Not only does zebrafish mirror human eye pathology better than current rodent models, with a highly preserved developmental pathway and, unlike mice, human-like cone-dominant vision; the model also allows for early high-throughput developmental studies, with fully functional eyes as soon as 5pdf. So, you can imagine how delighted we were to come across Dr. Jakub Famulski’s fascinating work on the anterior eye segment with zebrafish. We only hope you will also enjoy reading about it…

Source: University of Kentucky
By: Jenny Wells

Jakub Famulski, an assistant professor of biology in the University of Kentucky College of Arts and Sciences, has received a grant for over $1.8 million from the National Institutes of Health to study the early formation of the anterior segment of the eye. The research has the potential to lead to more treatment options for patients with blinding disorders.

The Research Project Grant (R01), "Comprehensive analysis of periocular mesenchyme composition, specification, and function during anterior segment formation," will be funded by the National Eye Institute over the next five years. Famulski and his team will study the anterior segment of the eye (which includes the cornea, iris, ciliary muscle, drainage canals and pupil) which is critical for collecting and projecting light onto the back of the eye. Deficiencies in these tissues are considered anterior segment dysgenesis (ASD) blinding disorders, and the tissues are also a critical regulator of intraocular pressure, a major indicator for glaucoma.

Famulski and his team will use the embryos of zebrafish to study the very early development of these critical visual components.

"Zebrafish eyes follow a highly-conserved path of development with that of humans and are an excellent system for studying early embryonic development of the visual system," Famulski said.

The project will center on three main goals:

  • Identify behavior of the anterior segment cells, that will give rise to all of the functional tissues. The team will use state-of-the-art molecular techniques, such as CRISPR, in combination with imaging technologies, such as light sheet microscopy, to achieve this goal.
  • Assemble a detailed readout of the molecular identity of these early progenitor cells. Gene expression will be compared between various populations of the anterior segment progenitor cells using RNA sequencing technology. This information will be necessary for any future attempts at stem cell therapy in ASD patients.
  • Correlate the findings by screening panels of ASD patients for mutations in genes identified in their work with zebrafish. The screening will be done in collaboration with Michael Walter, a professor in the Department of Medical Genetics at the University of Alberta.

"More than 50 percent of ASD cases have no definitive genetic explanation and we hope our work will lower that number in order to give clinicians more treatment or counseling options," Famulski said.

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