Treatment of Inherited Eye Defects by Systemic Hematopoietic Stem Cell Transplantation.

Abstract

PURPOSE:

Cystinosis is caused by a deficiency in the lysosomal cystine transporter, cystinosin (CTNS gene), resulting in cystine crystal accumulation in tissues. In eyes, crystals accumulate in the cornea causing photophobia and eventually blindness. Hematopoietic stem progenitor cells (HSPCs) rescue the kidney in a mouse model of cystinosis. We investigated the potential for HSPC transplantation to treat corneal defects in cystinosis.

METHODS:

We isolated HSPCs from transgenic DsRed mice and systemically transplanted irradiated Ctns-/- mice. A year posttransplantation, we investigated the fate and function of HSPCs by in vivo confocal and fluorescence microscopy (IVCM), quantitative RT-PCR (RT-qPCR), mass spectrometry, histology, and by measuring the IOP. To determine the mechanism by which HSPCs may rescue disease cells, we transplanted Ctns-/- mice with Ctns-/- DsRed HSPCs virally transduced to express functional CTNS-eGFP fusion protein.

RESULTS:

We found that a single systemic transplantation of wild-type HSPCs prevented ocular pathology in the Ctns-/- mice. Engraftment-derived HSPCs were detected within the cornea, and also in the sclera, ciliary body, retina, choroid, and lens. Transplantation of HSPC led to substantial decreases in corneal cystine crystals, restoration of normal corneal thickness, and lowered IOP in mice with high levels of donor-derived cell engraftment. Finally, we found that HSPC-derived progeny differentiated into macrophages, which displayed tunneling nanotubes capable of transferring cystinosin-bearing lysosomes to diseased cells.

CONCLUSIONS:

To our knowledge, this is the first demonstration that HSPCs can rescue hereditary corneal defects, and supports a new potential therapeutic strategy for treating ocular pathologies.

• Authors: Celine J Rocca, Alexander Kreymerman, Sarah N Ur, Katie E Frizzi, Swati Naphade, Athena Lau, Tammy Tran, Nigel A Calcutt, Jeffrey L Goldberg, Stephanie Cherqui
• Journal: Investigative ophthalmology & visual science (Invest Ophthalmol Vis Sci) Vol. 56 Issue 12 Pg. 7214-23 (Nov 2015) ISSN: 1552-5783 [Electronic] United States
• PMID: 26540660 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)

Topics

• Animals
• Cells, Cultured
• Cystinosis (genetics, therapy)
• Disease Models, Animal
• Eye Diseases (congenital, genetics, therapy)
• Hematopoietic Stem Cell Transplantation (methods)
• Mice
• Mice, Inbred C57BL
• Mice, Transgenic