Sensory physiology, anatomy and immunohistochemistry of Rohon‐Beard neurones in embryos of Xenopus laevis.

Rohon‐Beard neurones show substance P‐like immunoactivity in their somas and in their centrally projecting axons. Peripherally, the morphology of their free nerve endings within the trunk skin has been shown using horseradish peroxidase staining. The excitation of Rohon‐Beard neurones by natural and electrical stimulation of the skin has been examined using intracellular micro‐electrodes in the late embryo of Xenopus laevis. Rohon‐Beard cells are sensitive to transient, local indentation of the trunk skin, responding with one or a few impulses. They adapt rapidly to repeated stimulation. They can also be excited by a brief current pulse to the skin. They are not sensitive to slow indentation of the skin, nor are they excited by epithelial action potentials. The responses to skin stimulation are not abolished by a Ringer solution containing 12 mM‐Mg2+ and only 0.5 mM‐Ca2+. Intracellularly evoked action potentials in single Rohon‐Beard cells are sometimes sufficient to evoke sustained episodes of fictive swimming. The results indicate that Rohon‐Beard cells are responsible for detecting light touch stimuli to the embryo's body and for initiating swimming in response to this stimulus.

[1]  A. Roberts,et al.  The early development of the primary sensory neurones in an amphibian embryo: a scanning electron microscope study. , 1983, Journal of embryology and experimental morphology.

[2]  A. Roberts,et al.  The anatomy of two functional types of mechanoreceptive 'free' nerve-ending in the head skin of Xenopus embryos , 1983, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[3]  T. Ritchie,et al.  Immunohistochemical studies on the distribution and origin of candidate peptidergic primary afferent neurotransmitters in the spinal cord of an elasmobranch fish, the atlantic stingray (Dasyatis sabina) , 1983, The Journal of comparative neurology.

[4]  N. Spitzer Voltage‐ and stage‐development uncoupling of Rohon‐Beard neurones during embryonic development of Xenopus tadpoles , 1982, The Journal of physiology.

[5]  J. Bixby,et al.  The appearance and development of chemosensitivity in Rohon—Beard neurones of the Xenopus spinal cord , 1982, The Journal of physiology.

[6]  A. Roberts,et al.  The central nervous origin of the swimming motor pattern in embryos of Xenopus laevis. , 1982, The Journal of experimental biology.

[7]  J. Buchanan,et al.  Activities of identified interneurons, motoneurons, and muscle fibers during fictive swimming in the lamprey and effects of reticulospinal and dorsal cell stimulation. , 1982, Journal of neurophysiology.

[8]  J. Clarke,et al.  The neuroanatomy of an amphibian embryo spinal cord. , 1982, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[9]  S. Adachi,et al.  The genesis and transmission of epidermal potentials in an amphibian embryo. , 1981, Developmental biology.

[10]  M. Kemali,et al.  Substance P-, Met-enkephalin- and somatostatin-like immunoreactivity distribution in the frog spinal cord , 1981, Neuroscience Letters.

[11]  S. Hunt,et al.  An immunohistochemical study of neuronal populations containing neuropeptides or γ-aminobutyrate within the superficial layers of the rat dorsal horn , 1981, Neuroscience.

[12]  H. Takagi,et al.  Regional distribution of substance P‐like immunoreactivity in the frog brain and spinal cord: Immunohistochemical analysis , 1981, The Journal of comparative neurology.

[13]  J. Lamborghini,et al.  Rohon‐beard cells and other large neurons in Xenopus embryos originate during gastrulation , 1980, The Journal of comparative neurology.

[14]  Eugene Roberts,et al.  The origin, distribution and synaptic relationships of substance P axons in rat spinal cord , 1979, The Journal of comparative neurology.

[15]  T. Hökfelt,et al.  Distribution of substance P-like immunoreactivity in the central nervous system of the rat—I. Cell bodies and nerve terminals , 1978, Neuroscience.

[16]  M. C. Citron,et al.  The jet stream microbeveler: an inexpensive way to bevel ultrafine glass micropipettes. , 1978, Science.

[17]  I. Kanazawa,et al.  The distribution of substance P immunoreactive fibers in the rat central nervous system , 1978, The Journal of comparative neurology.

[18]  S L Palay,et al.  Ultrastructural identification of substance P cells and their processes in rat sensory ganglia and their terminals in the spinal cord by immunocytochemistry. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[19]  A. Roberts,et al.  The anatomy and function of 'free' nerve endings in an amphibian skin sensory system , 1977, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[20]  A. Roberts Neuronal growth cones in an amphibian embryo , 1976, Brain Research.

[21]  N. Spitzer,et al.  Development of the action potential in embryo amphibian neuronsin vivo , 1976, Brain Research.

[22]  N. Spitzer The ionic basis of the resting potential and a slow depolarizing response in Rohon‐Beard neurones of Xenopus tadpoles. , 1976, The Journal of physiology.

[23]  C. Rovainen,et al.  Electrical activity of myotomal muscle fibers, motoneurons, and sensory dorsal cells during spinal reflexes in lampreys. , 1971, Journal of neurophysiology.

[24]  D. Baylor,et al.  Specific modalities and receptive fields of sensory neurons in CNS of the leech. , 1968, Journal of neurophysiology.

[25]  A. Hughes The development of the primary sensory system in Xenopus laevis (Daudin). , 1957, Journal of anatomy.

[26]  H. Whiting Nervous structure of the spinal cord of the young larval brook-lamprey. , 1948, The Quarterly journal of microscopical science.

[27]  G. E. Coghill,et al.  Correlated anatomical and physiological studies of the growth of the nervous system of amphibia. II. The afferent system of the head of amblystoma , 1916 .

[28]  S. Landis,et al.  Neuronal growth cones. , 1983, Annual review of physiology.

[29]  V. Chan‐Palay Ultrastructural identification ofsubstance Pcells andtheir processes inratsensory ganglia andtheir terminals inthespinal cordbyimmunocytochemistry , 1977 .

[30]  W. Wickelgren,et al.  Sensory cells in the spinal cord of the sea lamprey , 1971, The Journal of physiology.