Literature DB >> 1460116

Transient expression of GABA immunoreactivity in the developing rat spinal cord.

W Ma1, T Behar, J L Barker.   

Abstract

The development of GABAergic neurons in the spinal cord of the rat has been investigated by immunocytochemical staining of frozen sections with anti-gamma-aminobutyric acid (GABA) antiserum. In the cervical cord, GABA-immunoreactive fibers first appeared at embryonic day (E) 13 in the presumptive white matter within the ventral commissure, ventral funiculus, and dorsal root entrance zone, and in the ventral roots. There were no GABA-immunoreactive cell bodies detected at this age. By E14, motoneurons, the earliest generated spinal cells, were the first cell population to become GABA-immunoreactive at the cell body level. Thereafter, GABA-immunoreactive neurons increased progressively in number and extended from ventral to dorsal regions. GABA-immunoreactive relay neurons within lamina I of the dorsal horn were initially detected at E17. Interneurons in the substantia gelatinosa, the latest generated cells in the spinal cord, were also the last to express the GABA immunoreactivity at E18. Immunoreactive neurons peaked in intensity and extent at E18 and 19. GABA immunoreactivity was only detectable in neurons within the intermediate and marginal zones 1-3 days after they withdrew from the cell cycle. This contrasts to glutamate decarboxylase immunoreactivity, which is detected in precursor cells in the ventricular zone prior to, or during, withdrawal from the cell cycle. Toward the end of gestation, GABA immunoreactivity declined in intensity and extent. This regression began in the ventral horn of the cervical region and ended in the dorsal horn of the lumbosacral region. During the first week after birth, immunoreactivity in motoneurons and in many other neurons within the ventral horn, intermediate gray, and deeper layers of the dorsal horn disappeared, and only in those neurons predominantly within the superficial layers of the dorsal horn did it persist into adulthood. Thus, the expression and regression of GABA immunoreactivity in the spinal cord followed ventral-to-dorsal, rostral-to-caudal, and medial-to-lateral gradients. These observations indicate that the majority of embryonic spinal neurons pass through a stage of transient expression of GABA immunoreactivity. The functional significance of this transient expression is unknown, but it coincides with the period of intense neurite growth of motoneurons, sensory neurons, and interneurons, and of neuromuscular junction formation, suggesting that the transient presence of GABA may play an important role in the differentiation of sensorimotor neuronal circuits.

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Year:  1992        PMID: 1460116     DOI: 10.1002/cne.903250210

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  16 in total

1.  Postnatal phenotype and localization of spinal cord V1 derived interneurons.

Authors:  Francisco J Alvarez; Philip C Jonas; Tamar Sapir; Robert Hartley; Maria C Berrocal; Eric J Geiman; Andrew J Todd; Martyn Goulding
Journal:  J Comp Neurol       Date:  2005-12-12       Impact factor: 3.215

2.  Segmental, synaptic actions of commissural interneurons in the mouse spinal cord.

Authors:  Katharina A Quinlan; Ole Kiehn
Journal:  J Neurosci       Date:  2007-06-13       Impact factor: 6.167

3.  Embryonically expressed GABA and glutamate drive electrical activity regulating neurotransmitter specification.

Authors:  Cory M Root; Norma A Velázquez-Ulloa; Gabriela C Monsalve; Elena Minakova; Nicholas C Spitzer
Journal:  J Neurosci       Date:  2008-04-30       Impact factor: 6.167

4.  Prominent expression of two forms of glutamate decarboxylase in the embryonic and early postnatal rat hippocampal formation.

Authors:  S T Dupuy; C R Houser
Journal:  J Neurosci       Date:  1996-11-01       Impact factor: 6.167

5.  Differential response of cortical plate and ventricular zone cells to GABA as a migration stimulus.

Authors:  T N Behar; A E Schaffner; C A Scott; C O'Connell; J L Barker
Journal:  J Neurosci       Date:  1998-08-15       Impact factor: 6.167

Review 6.  Synaptic control of motoneuronal excitability.

Authors:  J C Rekling; G D Funk; D A Bayliss; X W Dong; J L Feldman
Journal:  Physiol Rev       Date:  2000-04       Impact factor: 37.312

7.  Co-localization of serotonin and GABA in neurons of the Xenopus laevis retina.

Authors:  B S Zhu; C Straznicky
Journal:  Anat Embryol (Berl)       Date:  1993-06

8.  Motoneuron replacement for reinnervation of skeletal muscle in adult rats.

Authors:  Robert M Grumbles; Vania W Almeida; Gizelda T B Casella; Patrick M Wood; Kamondanai Hemstapat; Christine K Thomas
Journal:  J Neuropathol Exp Neurol       Date:  2012-10       Impact factor: 3.685

9.  Mechanisms of GABA and glycine depolarization-induced calcium transients in rat dorsal horn neurons.

Authors:  D B Reichling; A Kyrozis; J Wang; A B MacDermott
Journal:  J Physiol       Date:  1994-05-01       Impact factor: 5.182

10.  A developmental shift from GABAergic to glycinergic transmission in the central auditory system.

Authors:  V C Kotak; S Korada; I R Schwartz; D H Sanes
Journal:  J Neurosci       Date:  1998-06-15       Impact factor: 6.167

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