Literature DB >> 19576270

Colocalization of neuropeptides with calcium-binding proteins in the claustral interneurons during postnatal development of the rat.

Przemysław Kowiański1, Jerzy Dziewiatkowski, Joanna M Moryś, Katarzyna Majak, Sławomir Wójcik, Lawrence R Edelstein, Grazyna Lietzau, Janusz Moryś.   

Abstract

The claustrum is a relatively large telencephalic structure, situated close to the border of the neo- and allocortical regions. Its neuronal population consists of glutamatergic, projecting neurons and GABA-ergic interneurons, characterized by occurrence of numerous additional biochemical markers. The postnatal development of these latter neurons has not been extensively studied. Revealing the characteristic patterns of colocalizations between selected markers may shed some light on their function and origin. We investigated the colocalization patterns between three neuropeptides: neuropeptide Y, somatostatin, vasoactive intestinal polypeptide and three calcium-binding proteins: calbindin D28k, calretinin, parvalbumin in the interneurons of the rat claustrum during a four-month postnatal period (P0-P120; P: postnatal day). Our studies revealed the following types of colocalizations: neuropeptide Y with calbindin D28k, calretinin or parvalbumin; somatostatin with calbindin D28k; vasoactive intestinal polypeptide with calretinin. Only vasoactive intestinal polypeptide- and calretinin-containing, double-labeled neurons were present at the day of birth, whereas the other double-labeled neurons appeared at later stages of development. The ratios of colocalizing neurons to single-labeled neurons in each type of colocalization were differentiated and reached the highest value (51%) for vasoactive intestinal polypeptide- and calretinin-double-labeled neurons. In conclusion, the claustral interneurons represent differentiated population in respect to the occurrence of neuropeptides and calcium-binding proteins. The expression of studied substances is changing during the postnatal period.

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Year:  2009        PMID: 19576270     DOI: 10.1016/j.brainresbull.2009.06.020

Source DB:  PubMed          Journal:  Brain Res Bull        ISSN: 0361-9230            Impact factor:   4.077


  7 in total

1.  The catecholaminergic innervation of the claustrum of the pig.

Authors:  Andrea Pirone; Vincenzo Miragliotta; Federica Ciregia; Elisabetta Giannessi; Bruno Cozzi
Journal:  J Anat       Date:  2017-10-01       Impact factor: 2.610

2.  Claustrum circuit components for top-down input processing and cortical broadcast.

Authors:  Michael G White; Brian N Mathur
Journal:  Brain Struct Funct       Date:  2018-08-14       Impact factor: 3.270

3.  Hypotheses relating to the function of the claustrum.

Authors:  John Smythies; Lawrence Edelstein; Vilayanur Ramachandran
Journal:  Front Integr Neurosci       Date:  2012-08-02

4.  Expression of calcium-binding proteins and selected neuropeptides in the human, chimpanzee, and crab-eating macaque claustrum.

Authors:  Andrea Pirone; Maura Castagna; Alberto Granato; Antonella Peruffo; Francesca Quilici; Laura Cavicchioli; Ilaria Piano; Carla Lenzi; Bruno Cozzi
Journal:  Front Syst Neurosci       Date:  2014-05-26

5.  Calretinin immunoreactivity in the claustrum of the rat.

Authors:  Rastislav Druga; Martin Salaj; Filip Barinka; Lawrence Edelstein; Hana Kubová
Journal:  Front Neuroanat       Date:  2015-01-20       Impact factor: 3.856

6.  On the G Protein-Coupled Receptor Neuromodulation of the Claustrum.

Authors:  Dasiel O Borroto-Escuela; Kjell Fuxe
Journal:  Neurochem Res       Date:  2019-06-06       Impact factor: 3.996

7.  Identification of Mouse Claustral Neuron Types Based on Their Intrinsic Electrical Properties.

Authors:  Martin Graf; Aditya Nair; Kelly L L Wong; Yanxia Tang; George J Augustine
Journal:  eNeuro       Date:  2020-07-31
  7 in total

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