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Published in

Elsevier, Progress in Retinal and Eye Research, 1(23), p. 53-89, 2004

DOI: 10.1016/j.preteyeres.2003.10.003

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Mitochondrial dysfunction as a cause of optic neuropathies

Journal article published in 2004 by Valerio Carelli ORCID, Fred N. Ross-Cisneros, Alfredo A. Sadun
This paper is available in a repository.
This paper is available in a repository.

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Abstract

Mitochondria are increasingly recognized as central players in the life and death of cells and especially of neurons. The energy-dependence of retinal ganglion cells (RGC) and their axons, which form the optic nerve, is singularly skewed. In fact, while mitochondria are very abundant in the initial, unmyelinated part of the axons anterior to the lamina cribrosa, their number suddenly decreases as the myelin sheath begins more posteriorly. The vascular system also presents different blood–brain barrier properties anterior and posterior to the lamina, possibly reflecting the different metabolic needs of the optic nerve head (unmyelinated) and of the retrobulbar optic nerve (myelinated).