Literature DB >> 1409711

Membrane and synaptic properties of developing lateral geniculate nucleus neurons during retinogeniculate axon segregation.

C A White1, M Sur.   

Abstract

During the first postnatal month in the ferret (Mustela putorius furo), the projections from the retina to the lateral geniculate nucleus (LGN) become segregated into eye-specific layers and ON and OFF sublayers, a process that is thought to depend in part on neuronal activity. Remarkably, virtually nothing is known about the physiological features of LGN neurons during this period. We have recorded intracellularly from 46 A-layer neurons in slices of the ferret LGN between the ages of postnatal days 7 and 33. The passive membrane properties and current-voltage relationships of the developing neurons were similar in many, though not all, respects to those of adult LGN neurons. Action potentials in younger animals were smaller in amplitude and longer in duration than in older animals, but cells at all ages were capable of producing spike trains whose latency and spike number varied with stimulus intensity. In addition, cells at all ages responded with low-threshold potentials upon release from hyperpolarization. Slightly more than half of the LGN neurons responded to optic tract stimulation with excitatory postsynaptic potentials (EPSPs), inhibitory postsynaptic potentials (IPSPs), or EPSP-IPSP pairs, beginning with the youngest ages. Thus, as early as the second postnatal week, and much before the onset of pattern vision, LGN neurons have many of the membrane and synaptic properties of adult thalamic neurons. These data are consistent with LGN cells playing a significant role in activity-dependent reshaping of the retinogeniculate pathway.

Entities:  

Mesh:

Year:  1992        PMID: 1409711      PMCID: PMC50231          DOI: 10.1073/pnas.89.20.9850

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  26 in total

1.  Retinogeniculate EPSPs recorded intracellularly in the ferret lateral geniculate nucleus in vitro: role of NMDA receptors.

Authors:  M Esguerra; Y H Kwon; M Sur
Journal:  Vis Neurosci       Date:  1992-06       Impact factor: 3.241

2.  Ontogenesis of receptive field characteristics in the dorsal lateral geniculate nucleus of the rabbit.

Authors:  S C Rapisardi; K L Chow; L H Mathers
Journal:  Exp Brain Res       Date:  1975-03-27       Impact factor: 1.972

3.  Synapses formed by identified retinogeniculate axons during the segregation of eye input.

Authors:  G Campbell; C J Shatz
Journal:  J Neurosci       Date:  1992-05       Impact factor: 6.167

4.  Disruption of retinogeniculate afferent segregation by antagonists to NMDA receptors.

Authors:  J O Hahm; R B Langdon; M Sur
Journal:  Nature       Date:  1991-06-13       Impact factor: 49.962

5.  A Golgi study of dendritic development in the dorsal lateral geniculate nucleus of normal ferrets.

Authors:  J K Sutton; J K Brunso-Bechtold
Journal:  J Comp Neurol       Date:  1991-07-01       Impact factor: 3.215

6.  A fast transient potassium current in thalamic relay neurons: kinetics of activation and inactivation.

Authors:  J R Huguenard; D A Coulter; D A Prince
Journal:  J Neurophysiol       Date:  1991-10       Impact factor: 2.714

7.  Properties of a hyperpolarization-activated cation current and its role in rhythmic oscillation in thalamic relay neurones.

Authors:  D A McCormick; H C Pape
Journal:  J Physiol       Date:  1990-12       Impact factor: 5.182

8.  Slow inactivation of a TEA-sensitive K current in acutely isolated rat thalamic relay neurons.

Authors:  J R Huguenard; D A Prince
Journal:  J Neurophysiol       Date:  1991-10       Impact factor: 2.714

9.  Functional properties of a slowly inactivating potassium current in guinea pig dorsal lateral geniculate relay neurons.

Authors:  D A McCormick
Journal:  J Neurophysiol       Date:  1991-10       Impact factor: 2.714

10.  The dorsal lateral geniculate nucleus of the normal ferret and its postnatal development.

Authors:  D C Linden; R W Guillery; J Cucchiaro
Journal:  J Comp Neurol       Date:  1981-12-01       Impact factor: 3.215

View more
  8 in total

1.  Activity-dependent patterning of retinogeniculate axons proceeds with a constant contribution from AMPA and NMDA receptors.

Authors:  C D Hohnke; S Oray; M Sur
Journal:  J Neurosci       Date:  2000-11-01       Impact factor: 6.167

2.  T-type Ca2+ channels encode prior neuronal activity as modulated recovery rates.

Authors:  M Uebachs; C Schaub; E Perez-Reyes; H Beck
Journal:  J Physiol       Date:  2006-01-19       Impact factor: 5.182

3.  Postnatal development of membrane properties and delta oscillations in thalamocortical neurons of the cat dorsal lateral geniculate nucleus.

Authors:  M Pirchio; J P Turner; S R Williams; E Asprodini; V Crunelli
Journal:  J Neurosci       Date:  1997-07-15       Impact factor: 6.167

4.  Maturation of neuronal form and function in a mouse thalamo-cortical circuit.

Authors:  R A Warren; E G Jones
Journal:  J Neurosci       Date:  1997-01-01       Impact factor: 6.167

5.  Rapid acquisition of dendritic spines by visual thalamic neurons after blockade of N-methyl-D-aspartate receptors.

Authors:  M Rocha; M Sur
Journal:  Proc Natl Acad Sci U S A       Date:  1995-08-15       Impact factor: 11.205

6.  Stable properties of spontaneous EPSCs and miniature retinal EPSCs during the development of ON/OFF sublamination in the ferret lateral geniculate nucleus.

Authors:  C D Hohnke; M Sur
Journal:  J Neurosci       Date:  1999-01-01       Impact factor: 6.167

Review 7.  Emergence of order in visual system development.

Authors:  C J Shatz
Journal:  Proc Natl Acad Sci U S A       Date:  1996-01-23       Impact factor: 11.205

8.  The Thalamus as a Low Pass Filter: Filtering at the Cellular Level does Not Equate with Filtering at the Network Level.

Authors:  William M Connelly; Michael Laing; Adam C Errington; Vincenzo Crunelli
Journal:  Front Neural Circuits       Date:  2016-01-14       Impact factor: 3.492

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.