Literature DB >> 2729608

Postnatal development of the corticospinal tract in the rat. An ultrastructural anterograde HRP study.

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

Abstract

Horseradish-peroxidase was used to anterogradely label and thus to trace the growth of corticospinal axons in rats ranging in age from one day to six months. Three to eight HRP-gels were implanted in the left cerebral hemisphere of the cortex. In each spinal cord three levels were studied, the cervical intumescence (C5), the mid-thoracic region (T5) and the lumbar enlargement (L3). The methodology employed for the electron microscopic visualization of HRP has been described previously (Joosten et al. 1987a). The outgrowth of labelled unmyelinated corticospinal tract axons in the rat spinal cord primarily occurs during the first ten postnatal days. The outgrowth of the main wave of these fibres is preceded by a number of pathfinding axons, characterized by dilatations at their distal ends, the growth cones. By contrast, later appearing unmyelinated axons, which presumably grow along the pathfinding axons, do not exhibit such growth cones. The first labelled pioneer axons can be observed in the cervical intumescence at postnatal day one (P1), in the mid-thoracic region at day three (P3) and in the lumbar enlargement at day five (P5). Prior to the entrance of the axons, the prospective corticospinal area or the pre-arrival zone is composed of fascicles consisting of unlabelled, unmyelinated fibres surrounded by lucent amorphous structures. During the outgrowth phase of the corticospinal fibres some myelinated axons could be observed within the outgrowth area even before day 14. These axons, however, were never labelled. These findings strongly suggest that the outgrowth area, which is generally denoted as the pyramidal tract, contains other axons besides the corticospinal fibres (and glial cells).(ABSTRACT TRUNCATED AT 250 WORDS)

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2729608     DOI: 10.1007/bf00319587

Source DB:  PubMed          Journal:  Anat Embryol (Berl)        ISSN: 0340-2061


  33 in total

1.  Mechanisms at the axon tip regulate metabolic processes critical to axonal elongation.

Authors:  R J Lasek; M J Katz
Journal:  Prog Brain Res       Date:  1987       Impact factor: 2.453

2.  The development of glio-vascular relationships in the rat spinal cord. An electron microscopic study.

Authors:  C H Phelps
Journal:  Z Zellforsch Mikrosk Anat       Date:  1972

3.  Fine structural relationships between neurites and radial glial processes in developing mouse spinal cord.

Authors:  C K Henrikson; J E Vaughn
Journal:  J Neurocytol       Date:  1974-12

4.  A transient pyramidal tract projection from the visual cortex in the hamster and its removal by selective collateral elimination.

Authors:  D D O'Leary; B B Stanfield
Journal:  Brain Res       Date:  1986-06       Impact factor: 3.252

5.  Selective collateral elimination in early postnatal development restricts cortical distribution of rat pyramidal tract neurones.

Authors:  B B Stanfield; D D O'Leary; C Fricks
Journal:  Nature       Date:  1982-07-22       Impact factor: 49.962

6.  Unmyelinated axons in the pyramidal tract of the cat.

Authors:  A Thomas; L E Westrum; J L Devito; M A Biedenbach
Journal:  Brain Res       Date:  1984-05-28       Impact factor: 3.252

7.  Development of the motor system: hopping rats produced by prenatal irradiation.

Authors:  S P Hicks; C J D'Amato
Journal:  Exp Neurol       Date:  1980-10       Impact factor: 5.330

8.  Growth and maturation of the rat corticospinal tract.

Authors:  E G Jones; D J Schreyer; S P Wise
Journal:  Prog Brain Res       Date:  1982       Impact factor: 2.453

9.  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

10.  Growth cones, dying axons, and developmental fluctuations in the fiber population of the cat's optic nerve.

Authors:  R W Williams; M J Bastiani; B Lia; L M Chalupa
Journal:  J Comp Neurol       Date:  1986-04-01       Impact factor: 3.215

View more
  9 in total

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

Authors:  E A Joosten; D P Bär
Journal:  J Anat       Date:  1999-01       Impact factor: 2.610

2.  Descending Systems Direct Development of Key Spinal Motor Circuits.

Authors:  Calvin C Smith; Julian F R Paton; Samit Chakrabarty; Ronaldo M Ichiyama
Journal:  J Neurosci       Date:  2017-06-02       Impact factor: 6.167

3.  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

4.  Spatially restricted increase in polysialic acid enhances corticospinal axon branching related to target recognition and innervation.

Authors:  M M Daston; M Bastmeyer; U Rutishauser; D D O'Leary
Journal:  J Neurosci       Date:  1996-09-01       Impact factor: 6.167

5.  An ultrastructural double-labelling method: immunohistochemical localization of cell adhesion molecule L1 on HRP-labelled developing corticospinal tract axons in the rat.

Authors:  E A Joosten
Journal:  Histochemistry       Date:  1990

6.  Fetal spinal cord transplants support the development of target reaching and coordinated postural adjustments after neonatal cervical spinal cord injury.

Authors:  P S Diener; B S Bregman
Journal:  J Neurosci       Date:  1998-01-15       Impact factor: 6.167

Review 7.  Rodent Models of Developmental Ischemic Stroke for Translational Research: Strengths and Weaknesses.

Authors:  Mariangela Gennaro; Alessandro Mattiello; Tommaso Pizzorusso
Journal:  Neural Plast       Date:  2019-04-04       Impact factor: 3.599

8.  Strategies for regenerating injured axons after spinal cord injury - insights from brain development.

Authors:  Masaki Ueno; Toshihide Yamashita
Journal:  Biologics       Date:  2008-06

9.  Distinct oligodendrocyte populations have spatial preference and different responses to spinal cord injury.

Authors:  Elisa M Floriddia; Tânia Lourenço; Shupei Zhang; David van Bruggen; Markus M Hilscher; Petra Kukanja; João P Gonçalves Dos Santos; Müge Altınkök; Chika Yokota; Enric Llorens-Bobadilla; Sara B Mulinyawe; Mário Grãos; Lu O Sun; Jonas Frisén; Mats Nilsson; Gonçalo Castelo-Branco
Journal:  Nat Commun       Date:  2020-11-17       Impact factor: 14.919

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.