Astrocytes in the Optic Nerve Are Heterogeneous in Their Reactivity to Glaucomatous Injury

Author:

Zhu Ying12,Wang Rui13ORCID,Pappas Anthony C.1,Seifert Philip1,Savol Andrej45,Sadreyev Ruslan I.45,Sun Daniel1,Jakobs Tatjana C.1ORCID

Affiliation:

1. Department of Ophthalmology, Massachusetts Eye and Ear Infirmary/Schepens Eye Research Institute, Harvard Medical School, 20 Staniford Street, Boston, MA 02114, USA

2. Department of Ophthalmology, Stanford University, 1651 Page Mill Road, Palo Alto, CA 94304, USA

3. Department of Ophthalmology, The First Affiliated Hospital of Northwest University, Xi’an 710002, China

4. Department of Molecular Biology, Massachusetts General Hospital, Boston, MA 02114, USA

5. Department of Pathology, Massachusetts General Hospital and Harvard Medical School, 185 Cambridge St., Boston, MA 02114, USA

Abstract

The optic nerve head is thought to be the site of initial injury to retinal ganglion cell injury in glaucoma. In the initial segment of the optic nerve directly behind the globe, the ganglion cell axons are unmyelinated and come into direct contact to astrocytes, suggesting that astrocytes may play a role in the pathology of glaucoma. As in other parts of the CNS, optic nerve head astrocytes respond to injury by characteristic changes in cell morphology and gene expression profile. Using RNA-sequencing of glaucomatous optic nerve heads, single-cell PCR, and an in-vivo assay, we demonstrate that an up-regulation of astrocytic phagocytosis is an early event after the onset of increased intraocular pressure. We also show that astrocytes in the glial lamina of the optic nerve are apparently functionally heterogeneous. At any time, even in naïve nerves, some of the cells show signs of reactivity—process hypertrophy, high phagocytic activity, and expression of genetic markers of reactivity whereas neighboring cells apparently are inactive. A period of increased intraocular pressure moves more astrocytes towards the reactive phenotype; however, some cells remain unreactive even in glaucomatous nerves.

Funder

NIH

NIH Core

NIH NIDDK

National Natural Science Foundation of China

Massachusetts Lions Eye Research Fund

Bright Focus Foundation

Research to Prevent Blindness

Publisher

MDPI AG

Subject

General Medicine

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