July 1988
Volume 29, Issue 7
Free
Articles  |   July 1988
The extracellular matrix composition of the monkey optic nerve head.
Author Affiliations
  • J C Morrison
    Glaucoma Service, Wilmer Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • J A Jerdan
    Glaucoma Service, Wilmer Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • N L L'Hernault
    Glaucoma Service, Wilmer Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • H A Quigley
    Glaucoma Service, Wilmer Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Investigative Ophthalmology & Visual Science July 1988, Vol.29, 1141-1150. doi:
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      J C Morrison, J A Jerdan, N L L'Hernault, H A Quigley; The extracellular matrix composition of the monkey optic nerve head.. Invest. Ophthalmol. Vis. Sci. 1988;29(7):1141-1150.

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Abstract

The presence and distribution of laminin, heparan sulfate proteoglycan and collagen types I, III and IV were immunohistologically determined in cynomolgus monkey optic nerve heads using the avidin-biotin-peroxidase complex technique. Collagen types I and III were detected within the collagenous plates of the scleral lamina cribrosa, in the septa and pia mater of the postlaminar optic nerve and in blood vessel walls in all regions of the optic nerve head. Collagen type IV, laminin and heparan sulfate proteoglycans were all localized to the margins of the collagenous laminar plates of the scleral lamina cribrosa and along the margins of the optic nerve septa and the pia mater. All three components also appeared beneath the blood vessel endothelium throughout the optic nerve head. Within the lamina cribrosa, collagen types I and III occupy the core of the scleral laminar plates and may provide structural support for optic nerve bundles exiting the eye. The distribution of collagen type IV, laminin and heparan sulfate proteoglycan corresponds to basement membranes from two sources: vascular endothelial cells and glial cells lining the axonal bundles. Abnormalities of these substances may influence optic nerve function and susceptibility to elevated intraocular pressure by altering their mechanical support functions within the nerve head, by interfering with axonal nutrition, or both.

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