Cyclic adenosine monophosphate stimulation of axonal elongation.

Elevated concentrations of adenosine 3',5'-monophosphate induce a variety of cell movements. The role of adenosine 3',5'-monophosphate in promoting those movements associated with growth prompted our study of in vitro microtubule-dependent axonal elongation. Ganglia treated with adenosine 5'-monophosphate show no enhancement over controls; treatment with adenosine 3', 5'monophosphate or its dibutyryl derivative significantly enhances elongation, as measured by increases in both axonal numbers and length. Our study suggests that adenosine 3',5'-monophosphate promotes elongation by stimulation of microtubule assembly.

Modifications of tubulin heterogeneity during axonal growth in the embryonic nervous system.

Tectal plates of mouse embryos were used to analyze the heterogeneity of tubulin with high resolution isoelectric focusing, at time of appearance of the young neurons and axons. In the cold-labile pool of tubulin, isotypes 6 and 7 appear, and isotypes 1, 3, 11, 13 increase their relative quantities. The increase of the prominence of the alpha-group with regard to the beta-group in the cold-stable pool of tubulin raises the question as to the exact role of tubulin in the cold stability. A role of other specific microtubule components also appears probable.

The development of callosal and corticocortical innervation in the neocortex of the hamster.

The development of cortical afferentation by callosal and ipsilateral corticocortical fibers was studied in hamsters by transport of wheat germ agglutinin conjugated to horseradish peroxidase. Elongation of callosal axons (and possibly also of corticocortical fibers) started a couple of days before birth and extended through the first postnatal days. After a "waiting" period of a few days, axons were seen innervating restricted target sectors of the cortex. The zones of origin of these projections were initially exuberant, but they were subsequently trimmed down to overlap with the corresponding terminal fields.

[Synaptogenesis and axon collaterals coming from the white matter in the upper cervical cord of the 10 day (stage 36) chick embryo--Golgi and electron microscopic studies].

Our previous study with 3H-thymidine autoradiography showed that neurons of the zona spongiosa, the nucleus proprius of the dorsal horn, the zona intermedia and the ventralhorn differentiated earlier than those of the substantia gelatinosa and the neck and the base of the dorsal horn, and that neurons of the substantia gelatinosa which were the last to differentiate reached their final position at stage 36 (Fig. 1). In the upper cervical cord of chick embryos at stage 36 when all spinal neurons finished cell migration and the cytoarchitecture similar to that of the cat spinal cord (Rexed, 1952) could be recognized (cf. Figs. 1, 3B), we studied the distribution of synapses by the electron microphotomontage (Fig. 3 A) and the morphology of axon collaterals coming from the white matter by the Golgi method (Fig. 4), in order to examine i) which spinal neurons have synaptic contacts at this stage and ii) what part of the axon collateral makes synaptic contacts. In the white matter, synapses were numerous around the gray matter and they were few in the peripheral part along the external surface of the cord. The paucity of synapses in the peripheral part was explained by a finding that dendrites reaching the external surface of the cord were few in number at this stage (cf. Fig. 3 C). In the gray matter, synapses were more numerous and denser in the zona intermedia and the ventral horn than in the dorsal horn.(ABSTRACT TRUNCATED AT 250 WORDS)

[Ultrastructure of the hypophysiotropic region of the hypothalamus in early ontogenesis in rats]. / Ul'trastuktura gipofiziotropnoi oblasti gipotalamusa v rannem ontogeneze krysy

The results of electron microscopic studies have shown that the 16--18 days old rat embryos already have in the hypophysiotropic area some structures necessary for the realization of neuroendocrine regulations. In the arcuate nuclei, the neurosecretory cells differentiate which are capable to synthesize specific neurosecretory granules of 800--1,000 A in diameter. In the median eminence, the primary portal capillaries develop with which tanicytes and a few axon terminals make contact. One can see in the tanicytes the signs of active transport and accumulation of electron dense polymorphic material. All these phenomena are strengthen during the subsequent development. Hence, several days are before birth the neurosecretory and glial elements of the embryos show the signs of functional activity which strengthen during ontogenesis and are expressed most distinctly in the adult animals.

Electric fields, contact guidance and the direction of nerve growth.

Nerve orientation in response to electrical guidance cues in one direction and contact guidance cues in an orthogonal direction has been studied. Where neurites had a free choice between following contact guidance cues or electrical cues, the direction of nerve growth was determined predominantly by the vector of the applied electric field.

An examination of the evidence for the existence of preformed pathways in the neural tube of Xenopus laevis.

We have examined the neural tube in Xenopus laevis tadpoles to investigate the anatomical guidance elements which may be present in the presumptive marginal zone. With appropriate fixation protocols the neuroepithelial cells appeared in contact; electron microscopic observations failed to show any specialized intercellular spaces preceding the growing axons. The first fibres were found in the intercellular clefts between the neuroepithelial cells near the surface of the neural tube. Reconstructions of the neural tube from examination of serial 1 micron sections showed that the intercellular clefts are non-aligned at this stage and branching. Scanning electron microscopy of the surface of the neural tube confirmed that the intercellular spaces are non-aligned and often branch caudal to the growing front of descending axons. Thus to grow in a consistent direction the developing axons may have to make consistent and selective (specific) selections of pathway at numerous branch points if their growth is restricted to these intercellular clefts. As more axons grow along the neural tube, the intercellular clefts become wider, and the neuroepithelial cells bounding the clefts become indented. At later stages many fibres were observed with both scanning and transmission electron microscopy to grow along the surface of the neural tube. These changes in neuroepithelial cell morphology and fibre pathway allow axons to form bundles which take a fairly straight course in contrast to the winding path which must be taken by the first axons to grow through the intercellular clefts.

Chemotropic guidance of developing axons in the mammalian central nervous system.

In the developing nervous system, axons project considerable distances along stereotyped pathways to reach their targets. Axon guidance depends partly on the recognition of cell-surface and extracellular matrix cues derived from cells along the pathways. It has also been proposed that neuronal growth cones are guided by gradients of chemoattractant molecules emanating from their intermediate or final cellular targets. Although there is evidence that the axons of some peripheral neurons in vertebrates are guided by chemotropism and the directed growth of some central axons to their targets is consistent with such a mechanism, it remains to be determined whether chemotropism operates in the central nervous system. During development of the spinal cord, commissural axons are deflected towards a specialized set of midline neural epithelial cells, termed the floor plate, which could reflect guidance by substrate cues or by diffusible chemoattractant molecules. Here we provide evidence in support of chemotropic guidance by demonstrating that the rat floor-plate cells secrete a diffusible factor(s) that influences the pattern and orientation of commissural axon growth in vitro without affecting other embryonic spinal cord axons. These findings support the hypothesis that chemotropic mechanisms guide developing axons to their intermediate targets in the vertebrate CNS.

Pre-axonogenesis migration of afferent pioneer cells in the grasshopper embryo.

In insects, afferent neurons arise primarily from the ectodermal epithelium in the periphery and differentiate at the site of their precursor mitosis. Here we describe ectodermally derived cells that migrate away from their site of origin and initiate axonogenesis at a distant location. In embryonic grasshopper limb buds, the first two pairs of afferents to differentiate are the pair of Ti1 pioneers at the limb tip and the pair of Cx1 cells found at the base of the limb. While the Ti1 pioneers arise from the mitosis of a pioneer mother cell at the limb tip, the Cx1 cells are shown to emerge from the epithelium at circumferential positions that are approximately 150 degrees apart and that belong to different embryonic compartments. The cells migrate into contact with each other before initiating axonogenesis, and their axons then extend in a new direction that is orthogonal to the route of cell migration.

An improved silver stain for developing nervous tissue.

A reduced silver technique using physical development to stain embryonic nervous tissue is described. Brains are fixed in Bodian's fixative. Paraffin sections are pretreated with 1% chromic acid or 5% formol. They are impregnated with 0.01% silver nitrate dissolved in 0.1 M boric acid/sodium tetraborate buffer of pH 8 or with silver proteinate. Finally they are developed in a special physical developer which contains 0.1% silver nitrate, 0.01-0.1% formol as reducing agent, 2.5% sodium carbonate to buffer the solution at pH 10.3, 0.1% ammonium nitrate to prevent precipitation of silver hydroxide, and 5% tungstosilicic acid as a protective colloid. The development takes several minutes in this solution, thus the intensity of staining can be controlled easily. The method yields uniform, complete and reproducible staining of axons at all developmental stages of the nervous tissue and is easy to handle.

Local positional cues in the neuroepithelium guide retinal axons in embryonic Xenopus brain.

Growing retinal axons home to their distant target, the tectum, even when they are displaced from their normal pathway. This argues for long-range guidance mechanisms in the embryonic brain. Growth cones may orientate to diffusible attractants released from the target, as proposed in other systems, or they may use a stable distribution of positional information in the neuroepithelium. To distinguish between these possibilities, small pieces of the presumptive optic tract, through which retinal axons will normally grow, were rotated by approximately 90 degrees either clockwise or counterclockwise. When the retinal axons later encountered the rotated neuroepithelium, they also turned clockwise or counterclockwise, in correspondence with the direction of rotation. This demonstrates that long-range navigation of retinal axons in the vertebrate brain is based partly on stable, local positional factors, rather than on remote diffusible factors.

Correlation between growth form and movement and their dependence on neuronal age.

Neurites of superior cervical ganglion neurons from embryonic, perinatal, and adult rats extended at different rates when placed in tissue culture on similar collagen substrata. Using high resolution cinematography and a time-lapse video recording system, we concluded that these differences arise from variations in individual growth cone behavior. Growth cones of embryonic and perinatal neuronal origin exhibited high peak rates of advance and filopodial and lamellipodial excresences. Perinatal cones differed from embryonic ones in that they were somewhat larger, advanced in straighter paths, and retracted less, consequently translocating at 14 to 29 microns/hr compared with 8 to 22 microns/hr for embryonic cones (ranges of 4-hr means). The growth cones of neurons obtained from adult rats had scant cytoplasm and short branched filopodia, lacked definitive lamellipodia, and traversed the terrain at 4 to 13 microns/hr due to lack of high peak rates of advance and more time spent in stationary or minimal advance phases. Periodic pauses lasting 10 to 20 min, occurring every 20 to 90 min, interrupted the forward advance of growth cones of all ages. During pauses or slow forward movement, the growth cone displayed numerous filopodia whereas, during brief episodes when embryonic and perinatal growth cones moved at peak rates of 200 microns/hr or more, the cone periphery was predominantly lamellipodial. We conclude that the predominance of a lamellipodial or filopodial conformation correlates with the rate of growth cone advance and that age-dependent variations in neurite extension rates are related to differences in growth cone form and pattern of translocation. This is the first documentation of differing behavior of single growth cones of neurons of varying developmental ages in culture.

An identified cell is required for the formation of a major nerve during embryogenesis in the leech.

Investigations of the cues by which axonal growth cones navigate long distances to their targets have revealed the use of a rich and complex diversity of cellular and extracellular information. In the present study we describe one of the most conceptually simple pathfinding cues: a single identified cell in the leech, Hirudo medicinalis, that may guide axons several hundred micrometers to innervate a particular target. One of the stereotyped nerves of H. medicinalis is a "sex nerve" that projects from the anterior root of ganglion 6 [SNA (6)] to the male reproductive structures in the adjacent anterior segment. The pathway for SNA (6) is completely underlain by a single peripheral cell, here called the axonal runway cell (ARC), before axons enter the pathway. The ARC is apparently a nonneuronal cell that stains with a monoclonal antibody that recognizes leech muscle cells. The importance of the ARC for establishing SNA(6) was tested by ablating it before axons entered the pathway. When the ARC was killed either by physical disruption with a microelectrode, or by photoablation after filling it with the fluorescent dye Lucifer yellow, SNA(6) always failed to form, whereas all other nerves formed normally. Killing other peripheral cells in proximity to the ARC did not interfere with SNA(6) formation. Ablation of possible "pioneer neurons" for SNA(6) also did not prevent its formation. These results show that formation of a particular nerve requires only a single cell to serve as a guide for outgrowing processes.

Different subsets of axonal guidance cues are essential for sensory neurite outgrowth to cutaneous and muscle targets in the dorsal ramus of the embryonic chick.

The dorsal ramus nerve diverges dorsally from each spinal nerve to innervate the epaxial muscle and dermis that are derived in situ from each dermamyotome. The outgrowth of both the sensory and motor components of this nerve are sensitive to the proximity of the dermamyotome. Motoneurons display a direct target response that is not dependent upon the concurrent outgrowth of sensory neurites (Tosney: Dev. Biol. 122:540-588, 1987). Likewise, the outgrowth of sensory neurites could be directly dependent on the dermamyotome. Alternatively, sensory neurites could be dependent on motor axons that in turn require the dermamyotome for outgrowth. To distinguish between these possibilities, motor outgrowth was abolished by unilateral ventral neural tube deletion and the patterns of subsequent sensory neurite outgrowth were assessed. The cutaneous nerve branch formed in all cases. In contrast, neither of the epaxial muscle nerves formed in the absence of epaxial motoneuron outgrowth. Furthermore, sensory neurites could not be detected diverging into muscle from the cutaneous nerve or entering muscle via other novel routes. We conclude that motoneurons are essential for sensory outgrowth to epaxial muscle but not to cutaneous targets. It is clear that different subsets of navigational cues guide sensory afferents to muscle and to cutaneous destinations.