Nervous Structure of the Spinal Cord of the Young Larval Brook-Lamprey

1948 ◽  
Vol s3-89 (8) ◽  
pp. 359-383
Author(s):  
H. P. WHITING

1. A method for the study of the nervous system of vertebrate embryos by methylene blue vital staining is described. A reliable technique for rendering the preparations permanent is described. 2. An adaptation of the silver ‘on-the-slide’ method is given. 3. Three types of sensory intramedullary neuron are described in the spinal cord of recently hatched ammocoetes, or prides, of Lampetra planeri. All three are regarded as types of Rohon-Beard cell. 4. Four contemporary correlating types of cell are described in the cord: large internuncial neurons with a dendritic system which reaches the contralateral dorsal funiculus; cells of the Commissura Infima; oblique fibres, descending caudally from the sensory to the motor tracts; and small internuncial neurons with short dendrites. 5. The relations of the Miiller fibres in the trunk are described in part. 6. Two types of motor neuron have been found; the more fully developed corresponds to the primary motor neuron of aquatic larvae of other anamniote vertebrates. 7. The peripheral fibres of the somatic system of the trunk are described. 8. The neurological pattern revealed is compared with that in adult Lampetra: the divergences from the vertebrate pattern found in the cord of the adult are not found in the young ammocoete, which in this, as in so many respects, is a good prototype of gnathostome vertebrates. 9. The probable functional pattern is compared with that found in a similar stage of Amblystoma. Neurons of the correlating and motor system appear not to have been described before in ammocoetes less than 1 year old.

2002 ◽  
Vol 448 (4) ◽  
pp. 349-359 ◽  
Author(s):  
Martin Küchler ◽  
Karim Fouad ◽  
Oliver Weinmann ◽  
Martin E. Schwab ◽  
Olivier Raineteau

2002 ◽  
Vol 22 (4) ◽  
pp. 269-274 ◽  
Author(s):  
Tameko Kihira ◽  
Masaya Hironishi ◽  
Hidehiro Utunomiya ◽  
Tomoyoshi Kondo

2016 ◽  
Vol 122 (3) ◽  
pp. 730-737 ◽  
Author(s):  
Esperanza Recio-Pinto ◽  
Jose V. Montoya-Gacharna ◽  
Fang Xu ◽  
Thomas J. J. Blanck

Development ◽  
1998 ◽  
Vol 125 (6) ◽  
pp. 969-982 ◽  
Author(s):  
M. Ensini ◽  
T.N. Tsuchida ◽  
H.G. Belting ◽  
T.M. Jessell

The generation of distinct classes of motor neurons is an early step in the control of vertebrate motor behavior. To study the interactions that control the generation of motor neuron subclasses in the developing avian spinal cord we performed in vivo grafting studies in which either the neural tube or flanking mesoderm were displaced between thoracic and brachial levels. The positional identity of neural tube cells and motor neuron subtype identity was assessed by Hox and LIM homeodomain protein expression. Our results show that the rostrocaudal identity of neural cells is plastic at the time of neural tube closure and is sensitive to positionally restricted signals from the paraxial mesoderm. Such paraxial mesodermal signals appear to control the rostrocaudal identity of neural tube cells and the columnar subtype identity of motor neurons. These results suggest that the generation of motor neuron subtypes in the developing spinal cord involves the integration of distinct rostrocaudal and dorsoventral patterning signals that derive, respectively, from paraxial and axial mesodermal cell groups.


Development ◽  
1975 ◽  
Vol 33 (2) ◽  
pp. 403-417
Author(s):  
Brian P. Hayes ◽  
Alan Roberts

The distribution of intercellular junctions, other than synapses and their precursors, has beendescribed in the developing spinal cord of Xenopus laevis between the neurula andfree swimming tadpole stages. At the neurocoel, ventricular cells are joined in the apical contactzone by a sequence of junctions which usually has one or more intermediate junctions but often also includes close appositions, gap junctions and desmosomes. This apical complex is more diverse than that reported in other vertebrate embryos and between ependymal cells in the adult central nervous system. Gap junctions are also found between ventricular cells and their processes near the external cord surface. However, no other special junctions occur in this location under the basementlamella which surrounds the cord. Punctate intermediate junctions are generally distributed between undifferentiated and differentiating cells and their processes but were not found in neuropil after stage 28. These results are discussed in relation to cell movements during neural differentiation, possible effects on the freedom of movement of ions and molecules through extracellular pathways in the embryo, and possible intercytoplasmic pathways via gap junctions which may be responsible for the physiologically observed electrical coupling between neural tube cells.


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