» Articles » PMID: 3700717

Growth Cones, Dying Axons, and Developmental Fluctuations in the Fiber Population of the Cat's Optic Nerve

Overview
Journal J Comp Neurol
Specialty Neurology
Date 1986 Apr 1
PMID 3700717
Citations 22
Authors
Affiliations
Soon will be listed here.
Abstract

We have studied the rise and fall in the number of axons in the optic nerve of fetal and neonatal cats in relation to changes in the ultrastructure of fibers, and in particular, to the characteristics and spatiotemporal distribution of growth cones and necrotic axons. Axons of retinal ganglion cells start to grow through the optic nerve on the 19th day of embryonic development (E-19). As early as E-23 there are 8,000 fibers in the nerve close to the eye. Fibers are added to the nerve at a rate of approximately 50,000 per day from E-28 until E-39--the age at which the peak population of 600,000-700,000 axons is reached. Thereafter, the number decreases rapidly: About 400,000 axons are lost between E-39 and E-53. In contrast, from E-56 until the second week after birth the number of axons decreases at a slow rate. Even as late as postnatal day 12 (P-12) the nerve contains an excess of up to 100,000 fibers. The final number of fibers--140,000-165,000--is reached by the sixth week after birth. Growth cones of retinal ganglion cells are present in the optic nerve from E-19 until E-39. At E-19 and E-23 they have comparatively simple shapes but in older fetuses they are larger and their shapes are more elaborate. As early as E-28 many growth cones have lamellipodia that extend outward from the core region as far as 10 microns. These sheetlike processes are insinuated between bundles of axons and commonly contact 10 to 20 neighboring fibers in single transverse sections. At E-28 growth cones make up 2.0% of the fiber population; at E-33 they make up about 1.0%; from E-36 to E-39 they make up only 0.3% of the population. Virtually none are present in the midorbital part of the nerve on or after E-44. At all ages growth cones are more common at the periphery of the nerve than at its center. This central-to-peripheral gradient increases with age: at E-28 the density of growth cones is two times greater at the edge than at the center but by E-39 the density is four to five times greater. Necrotic fibers are observed as early as E-28 in all parts of the nerve. Their axoplasm is dark and mottled and often contains dense vesiculated structures.(ABSTRACT TRUNCATED AT 400 WORDS)

Citing Articles

Complement Targets Newborn Retinal Ganglion Cells for Phagocytic Elimination by Microglia.

Anderson S, Zhang J, Steele M, Romero C, Kautzman A, Schafer D J Neurosci. 2019; 39(11):2025-2040.

PMID: 30647151 PMC: 6507095. DOI: 10.1523/JNEUROSCI.1854-18.2018.


Cell proliferation and cytoarchitectural remodeling during spinal cord reconnection in the fresh-water turtle Trachemys dorbignyi.

Rehermann M, Santinaque F, Lopez-Carro B, Russo R, Trujillo-Cenoz O Cell Tissue Res. 2011; 344(3):415-33.

PMID: 21574060 PMC: 3131533. DOI: 10.1007/s00441-011-1173-y.


Distinct roles for laminin globular domains in laminin alpha1 chain mediated rescue of murine laminin alpha2 chain deficiency.

Gawlik K, Akerlund M, Carmignac V, Elamaa H, Durbeej M PLoS One. 2010; 5(7):e11549.

PMID: 20657839 PMC: 2906511. DOI: 10.1371/journal.pone.0011549.


Genetic control of interconnected neuronal populations in the mouse primary visual system.

Seecharan D, Kulkarni A, Lu L, Rosen G, Williams R J Neurosci. 2003; 23(35):11178-88.

PMID: 14657177 PMC: 6741036.


TrkB receptor signaling regulates developmental death dynamics, but not final number, of retinal ganglion cells.

Pollock G, Robichon R, Boyd K, Kerkel K, Kramer M, Lyles J J Neurosci. 2003; 23(31):10137-45.

PMID: 14602830 PMC: 6740848.