Literature DB >> 8708008

Genesis and fate of the perireticular thalamic nucleus during early development.

K L Earle1, J Mitrofanis.   

Abstract

A striking feature of the internal capsule during early development is that it is full of small neurones. Later, this group of neurones, called the perireticular thalamic nucleus, appears to have reduced in size, and only a few scattered cells are seen. In an effort to understand better the developmental history of the perireticular nucleus this study examines: i) the period of cell generation in the nucleus, ii) the magnitude of cell loss in the nucleus, and iii) the subsequent fate of cells in the nucleus during development. The perireticular cells are generated very early in development, being among the first generated in the thalamus (rats: E13-14; cats: E21-30). In rats, the first perireticular cells are generated at about the same developmental stage as the first subplate cells, which are among the first generated cells of the cortex: in cats, the first perireticular cells are generated well before those in the subplate (E24-30). In rats, the number of perireticular cells during developmental peaks at P5 (approximately 30,000) and then declines sharply (approximately 98%) by P15 (approximately 750), when adult-like patterns are seen. This dramatic loss of perireticular cells is due to both cell death and a migration of cells into the adjacent globus pallidus. The majority of the perireticular cells which migrate into the globus pallidus, however, are likely to die also. The presence of pyknotic profiles (indicators of dying cells) in the rat perireticular nucleus points to cell death as a contributor to the reduction in cell number during development. In this study, a period of relatively high pyknotic profile incidence (number of pyknotic cells per 1,000 "living" cells) is recorded in the perireticular nucleus over a 5 day period, from P2 to P7 (13.5-15.5). Similar values and patterns are recorded in the reticular nucleus and globus pallidus, except that in these structures, a period of relatively high pyknotic profile incidence (15-20) occurs over a shorter period (3 days; P2-5). Previous studies have suggested that some perireticular cells migrate into and settle within the adjacent globus pallidus. This study, with the use of long-term survivals after tracer injections in rats, shows that none (or very few) of these perireticular cells which migrate into the globus pallidus survive into more mature postnatal stages. Tracer (biotinylated dextran) was injected into the sensory nuclei of the dorsal thalamus at early stages (P7) and the rats were allowed to survive for either a day thereafter (to P8) or until well after the period of cell death was complete (to P16 or P21). In the short-term survivals (to P8), there are many dextran-labelled cells seen in the globus pallidus and in the perireticular nucleus. In the long-term survivals (to P16 or P21), by contrast, there are no dextran-labelled cells apparent in the globus pallidus or in the perireticular nucleus. It is likely that these cells in the globus pallidus, as with those in the perireticular nucleus, undergo cell death during development.

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Year:  1996        PMID: 8708008     DOI: 10.1002/(SICI)1096-9861(19960401)367:2<246::AID-CNE7>3.0.CO;2-5

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


  3 in total

1.  Combinatorial expression patterns of LIM-homeodomain and other regulatory genes parcellate developing thalamus.

Authors:  Y Nakagawa; D D O'Leary
Journal:  J Neurosci       Date:  2001-04-15       Impact factor: 6.167

2.  Morphological study of the perireticular nucleus in human fetal brains.

Authors:  Cumhur Murat Tulay; Levent Elevli; Uğur Duman; Ayşe Sarimehmetoğlu; Safiye Cavdar
Journal:  J Anat       Date:  2004-07       Impact factor: 2.610

3.  LacZ-reporter mapping of Dlx5/6 expression and genoarchitectural analysis of the postnatal mouse prethalamus.

Authors:  Luis Puelles; Carmen Diaz; Thorsten Stühmer; José L Ferran; Margaret Martínez-de la Torre; John L R Rubenstein
Journal:  J Comp Neurol       Date:  2020-06-18       Impact factor: 3.215

  3 in total

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