The relation of postsynaptic geometry to the number of presynaptic axons that innervate autonomic ganglion cells.

نویسندگان

  • D Purves
  • R I Hume
چکیده

We have studied the shape of rabbit ciliary ganglion cells in relation to the number of axons that innervate each neuron. Adult ganglion cells receive synapses from one to seven different preganglionic axons. Some neurons lack dendrites altogether, whereas others have complex arborizations of up to eight primary dendrites. The neurons that receive all of their synaptic contacts from a single preganglionic axon usually have no dendrites; on the other hand, multiply innervated ganglion cells receive synapses from a number of different axons that increases in proportion to the number of primary dendrites that they possess. A possible explanation of these results is that individual ciliary ganglion cells comprise a number of separate spatial domains, each of which is largely constrained to receive innervation from a single preganglionic axon.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Ultrastructural analysis of the distribution of synaptic boutons from labeled preganglionic axons on rabbit ciliary neurons.

The number of preganglionic inputs that innervate rabbit ciliary ganglion cells is directly correlated with the number of dendrites arising from each ganglion cell (Purves and Hume, 1981). In general, the innervation of multiply innervated ciliary neurons by individual preganglionic axons is regionally restricted to a portion of the postsynaptic surface that usually includes the cell body and s...

متن کامل

Regional innervation of rabbit ciliary ganglion cells by the terminals of preganglionic axons.

In the rabbit, ciliary ganglion neurons with dendrites maintain inputs from several different axons during the period of synaptic rearrangement that occurs in early postnatal life. Neurons without dendrites, on the other hand, lose the majority of their initial inputs and are innervated in maturity by the terminals of only one or two axons (Purves, D., and R.I. Hume (1981) J. Neurosci. 1: 441-4...

متن کامل

Cell-autonomous TrkB signaling in presynaptic retinal ganglion cells mediates axon arbor growth and synapse maturation during the establishment of retinotectal synaptic connectivity.

BDNF contributes to the activity-dependent establishment and refinement of visual connectivity. In Xenopus, BDNF applications in the optic tectum influence retinal ganglion cell (RGC) axon branching and promote synapse formation and stabilization. The expression patterns of BDNF and TrkB suggest that BDNF specifically regulates the maturation of RGC axons at the target. It is possible, however,...

متن کامل

Ganglionic Blocking Drugs and Nicotine

Transmission through autonomic ganglia is more complex than neurotransmission at the neuromuscular and postganglionic neuroeffector junctions and is subject to numerous pharmacological and physiological influences. In some ganglionic synapses, especially at parasympathetic ganglia, there is a simple presynaptic to postsynaptic cell relationship; in others, the presynaptic to postsynaptic cell r...

متن کامل

Relation of animal size to convergence, divergence, and neuronal number in peripheral sympathetic pathways.

The enormous range of animal size raises a fundamental problem: How do larger animals maintain adequate control of peripheral structures that are many times more massive and extensive than the homologous structures in smaller animals? To explore this question, we have determined neuronal number, the number of axons that innervate each neuron (convergence) and the number of neurons innervated by...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:
  • The Journal of neuroscience : the official journal of the Society for Neuroscience

دوره 1 5  شماره 

صفحات  -

تاریخ انتشار 1981