Literature DB >> 8026339

Development of specific muscle and cutaneous sensory projections in cultured segments of spinal cord.

K Sharma1, Z Korade, E Frank.   

Abstract

Development of sensory projections was studied in cultured spinal segments with attached dorsal root ganglia. In spinal segments from stage 30 (E6.5) and older chicken embryos, prelabeled muscle and cutaneous afferents established appropriate projections. Cutaneous afferents terminated solely within the dorsolateral laminae, whereas some muscle afferents (presumably Ia afferents) projected ventrally towards motoneurons. Development of appropriate projections suggests that sufficient cues are preserved in spinal segments to support the formation of modality-specific sensory projections. Further, because these projections developed in the absence of muscle or skin, these results show that the continued presence of peripheral targets is not required for the formation of specific central projections after stage 29 (E6.0). Development of the dorsal horn in cultured spinal segments was assessed using the dorsal midline as a marker. In ovo, this midline structure appears at stage 29. Lack of midline formation in stage 28 and 29 cultured spinal segments suggests that the development of the dorsal horn is arrested in this preparation. This is consistent with earlier reports suggesting that dorsal horn development may be dependent on factors outside the spinal cord. Because dorsal horn development is blocked in cultured spinal segments, this preparation makes it possible to study the consequences of premature ingrowth of sensory axons into the spinal cord. In chicken embryos sensory afferents reach the spinal cord at stage 25 (E4.5) but do not arborize within the gray matter until stage 30. During this period dorsal horn cells are still being generated. In spinal segments, only those segments that have developed a midline at the time of culture support the formation of midline at the time of culture support the formation of specific sensory projections.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1994        PMID: 8026339     DOI: 10.1242/dev.120.5.1315

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  7 in total

1.  The "waiting period" of sensory and motor axons in early chick hindlimb: its role in axon pathfinding and neuronal maturation.

Authors:  G Wang; S A Scott
Journal:  J Neurosci       Date:  2000-07-15       Impact factor: 6.167

2.  Restriction in cell fates of developing spinal cord cells transplanted to neural crest pathways.

Authors:  Z Korade; E Frank
Journal:  J Neurosci       Date:  1996-12-01       Impact factor: 6.167

3.  Reelin controls position of autonomic neurons in the spinal cord.

Authors:  J W Yip; Y P Yip; K Nakajima; C Capriotti
Journal:  Proc Natl Acad Sci U S A       Date:  2000-07-18       Impact factor: 11.205

4.  A sensory axon repellent secreted from ventral spinal cord explants is neutralized by antibodies raised against collapsin-1.

Authors:  I T Shepherd; Y Luo; F Lefcort; L F Reichardt; J A Raper
Journal:  Development       Date:  1997-04       Impact factor: 6.868

5.  Retinoid signaling is involved in governing the waiting period for axons in chick hindlimb.

Authors:  Guoying Wang; Sheryl A Scott
Journal:  Dev Biol       Date:  2008-06-21       Impact factor: 3.582

6.  Pathfinding of corticothalamic axons relies on a rendezvous with thalamic projections.

Authors:  Marie Deck; Ludmilla Lokmane; Sophie Chauvet; Caroline Mailhes; Maryama Keita; Mathieu Niquille; Michio Yoshida; Yutaka Yoshida; Cécile Lebrand; Fanny Mann; Elizabeth A Grove; Sonia Garel
Journal:  Neuron       Date:  2013-02-06       Impact factor: 17.173

7.  Somatotopic organization of central arbors from nociceptive afferents develops independently of their intact peripheral target innervation.

Authors:  William Olson; Wenqin Luo
Journal:  J Comp Neurol       Date:  2018-10-30       Impact factor: 3.215

  7 in total

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