Er. Tamm et al., NERVE-ENDINGS WITH STRUCTURAL CHARACTERISTICS OF MECHANORECEPTORS IN THE HUMAN SCLERAL SPUR, Investigative ophthalmology & visual science, 35(3), 1994, pp. 1157-1166
Purpose. The innervation of the scleral spur region was investigated t
o learn whether mechanoreceptors are present in this region. Methods.
Serial tangential sections and whole-mount preparations of the scleral
spur region of 18 human eyes of different ages were investigated with
electronmicroscopic and immunohistochemical methods. For immunohistoc
hemistry antibodies against neurofilament-proteins, synaptophysin, sub
stance P (SP), calcitonin gene-related peptide (CGRP), vasoactive inte
stinal polypeptide (VIP), neuropeptide Y (NPY), tyrosine-hydroxylase,
dopamine-beta-hydroxylase, and acetylcholinesterase were used. Results
. Club- or bulb-shaped nerve endings with a diameter of 5 mu m to 25 m
u m were identified in the scleral spur region throughout the whole ci
rcumference of the eyes. The terminals derive from myelinated axons wi
th a diameter of approximately 3 mu m and stain with antibodies agains
t neurofilament-proteins and synaptophysin but do not stain for tyrosi
ne-hydroxylase, dopamine-beta-hydroxylase, acetylcholinesterase, NPY,
VIP, SP, or CGRP. Electronmicroscopically, the endings contain abundan
t neurofilaments, granular and agranular vesicles of different sizes,
numerous mitochondria, and lysosome-like lamellated structures. The en
dings are incompletely ensheathed by Schwann cells. Those areas of the
cell membrane of the endings that are not covered by Schwann cells ar
e in intimate contact with the fibrillar connective tissue elements of
the scleral spur. Conclusion. These structural features are highly ch
aracteristic for mechanoreceptive nerve endings in other tissues of th
e human body. The authors therefore hypothesize that the club- or bulb
-shaped nerve endings in the human scleral spur are afferent mechanore
ceptors that measure stress or strain in the connective tissue element
s of the scleral spur. Such changes might be induced by ciliary muscle
contraction and/or by changes in intraocular pressure.