Fetal calf serum-mediated inhibition of neurite growth from ciliary ganglion neurons in vitro

1984 ◽  
Vol 12 (1) ◽  
pp. 29-39 ◽  
Author(s):  
G. E. Davis ◽  
S. D. Skaper ◽  
M. Manthorpe ◽  
G. Moonen ◽  
S. Varon
Keyword(s):  
Fetal Calf Serum ◽  
Calf Serum ◽  
Neurite Growth ◽  
Ciliary Ganglion ◽  
Ciliary Ganglion Neurons ◽  
Ganglion Neurons

GDNF and neurturin are target-derived factors essential for cranial parasympathetic neuron development

Development ◽  
2001 ◽  
Vol 128 (19) ◽  
pp. 3773-3782 ◽  
Author(s):  
Eri Hashino ◽  
Marlene Shero ◽  
Dirk Junghans ◽  
Hermann Rohrer ◽  
Jeffrey Milbrandt ◽  
...  
Keyword(s):  
Striate Muscle ◽  
Ciliary Ganglion ◽  
Neuron Development ◽  
Down Regulation ◽  
Eye Muscle ◽  
Ciliary Ganglion Neurons ◽  
Ganglion Neurons ◽  
Parasympathetic Neuron

During development, parasympathetic ciliary ganglion neurons arise from the neural crest and establish synaptic contacts on smooth and striate muscle in the eye. The factors that promote the ciliary ganglion pioneer axons to grow toward their targets have yet to be determined. Here, we show that glial cell line-derived neurotrophic factor (GDNF) and neurturin (NRTN) constitute target-derived factors for developing ciliary ganglion neurons. Both GDNF and NRTN are secreted from eye muscle located in the target and trajectory pathway of ciliary ganglion pioneer axons during the period of target innervation. After this period, however, the synthesis of GDNF declines markedly, while that of NRTN is maintained throughout the cell death period. Furthermore, both in vitro and in vivo function-blocking of GDNF at early embryonic ages almost entirely suppresses ciliary axon outgrowth. These results demonstrate that target-derived GDNF is necessary for ciliary ganglion neurons to innervate ciliary muscle in the eye. Since the down-regulation of GDNF in the eye is accompanied by down-regulation of GFRα1 and Ret, but not of GFRα2, in innervating ciliary ganglion neurons, the results also suggest that target-derived GDNF regulates the expression of its high-affinity coreceptors.

scholarly journals Laminin promotes neuritic regeneration from cultured peripheral and central neurons.

1983 ◽  
Vol 97 (6) ◽  
pp. 1882-1890 ◽  
Author(s):  
M Manthorpe ◽  
E Engvall ◽  
E Ruoslahti ◽  
F M Longo ◽  
G E Davis ◽  
...  
Keyword(s):  
Extracellular Matrix ◽  
Neurite Growth ◽  
Sensory Ganglia ◽  
Culture Methods ◽  
Fetal Rat ◽  
Extracellular Matrix Components ◽  
Ciliary Ganglion Neurons ◽  
Ganglion Neurons

The ability of axons to grow through tissue in vivo during development or regeneration may be regulated by the availability of specific neurite-promoting macromolecules located within the extracellular matrix. We have used tissue culture methods to examine the relative ability of various extracellular matrix components to elicit neurite outgrowth from dissociated chick embryo parasympathetic (ciliary ganglion) neurons in serum-free monolayer culture. Purified laminin from both mouse and rat sources, as well as a partially purified polyornithine-binding neurite promoting factor (PNPF-1) from rat Schwannoma cells all stimulate neurite production from these neurons. Laminin and PNPF-1 are also potent stimulators of neurite growth from cultured neurons obtained from other peripheral as well as central neural tissues, specifically avian sympathetic and sensory ganglia and spinal cord, optic tectum, neural retina, and telencephalon, as well as from sensory ganglia of the neonatal mouse and hippocampal, septal, and striatal tissues of the fetal rat. A quantitative in vitro bioassay method using ciliary neurons was used to (a) measure and compare the specific neurite-promoting activities of these agents, (b) confirm that during the purification of laminin, the neurite-promoting activity co-purifies with the laminin protein, and (c) compare the influences of antilaminin antibodies on the neurite-promoting activity of laminin and PNPF-1. We conclude that laminin and PNPF-1 are distinct macromolecules capable of expressing their neurite-promoting activities even when presented in nanogram amounts. This neurite-promoting bioassay currently represents the most sensitive test for the biological activity of laminin.

scholarly journals Choroid tissue supports the survival of ciliary ganglion neurons in vitro

1993 ◽  
Vol 13 (7) ◽  
pp. 3143-3154 ◽  
Author(s):  
LA Wentzek ◽  
CW Bowers ◽  
L Khairallah ◽  
G Pilar
Keyword(s):  
Ciliary Ganglion ◽  
Ciliary Ganglion Neurons ◽  
Ganglion Neurons

Regulation of neuronal K(+) currents by target-derived factors: opposing actions of two different isoforms of TGFbeta

Development ◽  
1999 ◽  
Vol 126 (18) ◽  
pp. 4157-4164
Author(s):  
J.S. Cameron ◽  
L. Dryer ◽  
S.E. Dryer
Keyword(s):  
Functional Expression ◽  
Developmental Expression ◽  
Ciliary Ganglion ◽  
Target Tissue ◽  
Intraocular Injection ◽  
Ciliary Ganglion Neurons ◽  
Ganglion Neurons ◽  
K Currents

The developmental expression of macroscopic Ca(2+)-activated K(+) currents in chick ciliary ganglion neurons is dependent on an avian ortholog of TGFbeta1, known as TGFbeta4, secreted from target tissues in the eye. Here we report that a different isoform, TGFbeta3, is also expressed in a target tissue of ciliary ganglion neurons. Application of TGFbeta3 inhibits the functional expression of whole-cell Ca(2+)-activated K(+) currents evoked by 12 hour treatment with either TGFbeta1 or beta-neuregulin-1 in ciliary ganglion neurons developing in vitro. TGFbeta3 had no effect on voltage-activated Ca(2+) currents. A neutralizing antiserum specific for TGFbeta3 potentiates stimulation of Ca(2+)-activated K(+) currents evoked by a target tissue (iris) extract in cultured ciliary ganglion neurons, indicating that TGFbeta3 is an inhibitory component of these extracts. Intraocular injection of TGFbeta3 causes a modest but significant inhibition of the expression of Ca(2+)-activated K(+) currents in ciliary ganglion neurons developing in vivo. Further, intraocular injection of a TGFbeta3-neutralizing antiserum stimulates expression of Ca(2+)-activated K(+) currents in ciliary ganglion neurons developing in vivo, indicating that endogenous TGFbeta3 regulates the functional expression of this current. The normal developmental expression of functional Ca(2+)-activated K(+) currents in ciliary ganglion neurons developing in vivo is therefore regulated by two different target-derived isoforms of TGFbeta, which produce opposing effects on the electrophysiological differentiation of these neurons.

scholarly journals Changes in the number of chick ciliary ganglion neuron processes with time in cell culture.

1987 ◽  
Vol 104 (2) ◽  
pp. 363-370 ◽  
Author(s):  
L W Role ◽  
G D Fischbach
Keyword(s):  
Cell Culture ◽  
Time Course ◽  
Culture Conditions ◽  
Ciliary Ganglion ◽  
Intact Cells ◽  
Dissociated Cell Culture ◽  
Ciliary Ganglion Neurons ◽  
Ganglion Neurons

The purpose of this study was to describe the shape of chick ciliary ganglion neurons dissociated from embryonic day 8 or 9 ganglia and maintained in vitro. Most of the neurons were multipolar during the first three days after plating, with an average of 6.0 processes extending directly from the cell body. The neurons became unipolar with time. The remaining primary process accounted for greater than 90% of the total neuritic arbor. This striking change in morphology was not due to the selective loss of multipolar cells, or to an obvious decline in the health of apparently intact cells. The retraction of processes was neither prevented nor promoted by the presence of embryonic muscle cells. Process pruning occurred to the same extent and over the same time course whether the cells were plated on a monolayer of embryonic myotubes or on a layer of lysed fibroblasts. Process retraction is not an inevitable consequence of our culture conditions. Motoneurons dissociated from embryonic spinal cords remained multipolar over the same period of time. We conclude that ciliary ganglion neurons breed true in dissociated cell culture in that the multipolar-unipolar transition reflects their normal, in vivo, developmental program.

Variation among acetylcholine receptor clusters induced by ciliary ganglion neurons in vitro

1988 ◽  
Vol 130 (1) ◽  
pp. 209-219 ◽  
Author(s):  
Janet M. Dubinsky ◽  
Megan Morgan ◽  
Gerald D. Fischbach
Keyword(s):  
Acetylcholine Receptor ◽  
Ciliary Ganglion ◽  
Ciliary Ganglion Neurons ◽  
Receptor Clusters ◽  
Ganglion Neurons

scholarly journals Differential labeling of the cell surface of single ciliary ganglion neurons in vitro.

1976 ◽  
Vol 73 (11) ◽  
pp. 4100-4104 ◽  
Author(s):  
N. K. Wessells ◽  
R. P. Nuttall ◽  
J. T. Wrenn ◽  
S. Johnson
Keyword(s):  
Cell Surface ◽  
Ciliary Ganglion ◽  
Ciliary Ganglion Neurons ◽  
Ganglion Neurons
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