Literature DB >> 3676848

An anterograde tracer study of the developing corticospinal tract in the rat: three components.

E A Joosten1, A A Gribnau, P J Dederen.   

Abstract

Light microscopic analysis of anterogradely transported wheat germ agglutinin-conjugated horseradish peroxidase (WGA-HRP) has been used to study the developing corticospinal tract (CST) in the rat. This study was carried out to examine the relationship between the site of injection within the cortex and the pattern of labelling of the developing CST in the spinal cord from postnatal day 1 (P1) through postnatal day 10 (P10). For this purpose the cortex was subdivided into 3 equal areas along the rostrocaudal axis: anterior, intermediate and posterior. After the operation the animals were allowed to survive for 24 h. The caudal extension of labelled CST axons originating in the anterior cortical area was restricted (L1 at P7 or P10) as compared with that of the CST fibres originating in the intermediate cortical area (S3 at P10). The axons of the posterior corticospinal (CS) neurones reach their most caudal extension in the spinal cord (T5) at P7 but then gradually disappear up till P14. Quantitative analysis of the amount of label along the length of the outgrowing CST fibres revealed the formation of a large stable peak at the level of the cervical enlargement after labelling of either the anterior or the intermediate cortical area. The formation of a second 'running' peak which moves caudally from mid-thoracic levels at P5 to mid-lumbar levels at P10 was only accomplished by labelling the intermediate cortical area and is probably caused by the accumulation of label in the growth cones at the distal ends of the outgrowing CST fibres. After labelling the posterior cortical area, no peaks could be detected, neither at the cervical nor at the lumbar intumescence. The major spinal grey termination field of the anterior CS neurones appeared to be the cervical intumescence, whereas the major spinal grey termination field of the intermediate CS neurones is the lumbar enlargement. By contrast, axons of posterior CS neurones never showed any outgrowth into the spinal grey matter at any level. Concluding, the developing CST in the rat consists of 3 components: the first having its originating neurones in the anterior part of the cortex and its termination field in the cervical intumescence; the second with its originating neurones in the intermediate part of the cortex and its termination field predominantly in the lumbar enlargement, and a third transient one, originating in the posterior cortex and gradually disappearing from spinal cord levels. Research using anterograde tracing techniques in combination with electron microscopy is necessary to further analyse these 3 different components.

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Year:  1987        PMID: 3676848     DOI: 10.1016/0165-3806(87)90070-8

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  18 in total

Review 1.  Axon guidance of outgrowing corticospinal fibres in the rat.

Authors:  E A Joosten; D P Bär
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2.  Proliferation and differentiation of progenitor cells throughout the intact adult rat spinal cord.

Authors:  P J Horner; A E Power; G Kempermann; H G Kuhn; T D Palmer; J Winkler; L J Thal; F H Gage
Journal:  J Neurosci       Date:  2000-03-15       Impact factor: 6.167

3.  Eph tyrosine kinase receptor EphA4 is required for the topographic mapping of the corticospinal tract.

Authors:  Alison J Canty; Ursula Greferath; Ann M Turnley; Mark Murphy
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4.  Patterns of maturation of somatotopical distribution of corticospinal neurons in postnatal rats. A WGA-HRP study.

Authors:  T Uozumi; H Nakamura; M Kawabuchi; T Kanaseki
Journal:  Anat Embryol (Berl)       Date:  1988

5.  A quantitative analysis of the development of the pyramidal tract in the cervical spinal cord in the rat.

Authors:  T G Gorgels; E J De Kort; H T Van Aanholt; R Nieuwenhuys
Journal:  Anat Embryol (Berl)       Date:  1989

6.  Biomaterial bridges enable regeneration and re-entry of corticospinal tract axons into the caudal spinal cord after SCI: Association with recovery of forelimb function.

Authors:  Kiran Pawar; Brian J Cummings; Aline Thomas; Lonnie D Shea; Ariel Levine; Sam Pfaff; Aileen J Anderson
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Authors:  T Savio; M E Schwab
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8.  Postnatal development of the corticospinal tract in the rat. An ultrastructural anterograde HRP study.

Authors:  E A Joosten; A A Gribnau; P J Dederen
Journal:  Anat Embryol (Berl)       Date:  1989

9.  Hemicerebellectomy and motor behaviour in rats. I. Development of motor function after neonatal lesion.

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Review 10.  Molecular logic of neocortical projection neuron specification, development and diversity.

Authors:  L C Greig; M B Woodworth; M J Galazo; H Padmanabhan; J D Macklis
Journal:  Nat Rev Neurosci       Date:  2013-10-09       Impact factor: 34.870

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