Literature DB >> 8226295

A quantitative study of the differentiation of microglial cells in the developing cerebral cortex in rats.

C H Wu1, C Y Wen, J Y Shieh, E A Ling.   

Abstract

The distribution of various morphological forms of microglia stained with lectin in different regions of postnatal rat brain was examined in 2 planes of section, coronal and sagittal. In the coronal sections (mediolateral plane) taken at the level of the optic chiasma, the lectin-labelled cells were examined in the gustatory (GU), lateral somatosensory (LSS), medial somatosensory (MSS), motor (MO) and cingulate (CI) cortex. In the sagittal sections (rostrocaudal plane), the lectin-labelled cells in the medial orbital (MOA), motor (MO) and primary visual area (PVA) were studied. The cells in the motor area in coronal plane were further analysed with reference to their distribution in each of the laminae (layers). Based on the variation of their external morphology which represents different degrees of differentiation, all lectin-labelled microglial cells of the above-mentioned regions in newborn (P0) and rats aged 4 d (P4) and 8 d (P8) postnatum were classified and quantified. In the mediolateral plane of any given age group, the most differentiated ramified cells were located in GU except in P8 rats where the cells were also concentrated in CI. Of the 3 regions in the rostrocaudal plane the majority of the more differentiated ramified cells at P0 were found in the PVA but were the major cell type in MO in P4 and P8 rats. For the distribution of cells in MO, the most differentiated cells were located in the intermediate zones. It was concluded from this study that microglial cells in the developing cerebrum showed a gradient of differentiation in relation to different regions of the cerebral cortex but this appeared to vary with age. Thus in the mediolateral plane in P0 and P4 rats, the gradient extended from GU to CI in a lateromedial fashion but in P8, in the direction towards MSS from GU and CI. In the sagittal section, the gradient was directed caudorostrally in P0 rats. In P4 and P8 rats, however, the gradient was from MO to both poles (MOA, PVA). In the motor cortex, the gradient was from the intermediate zone towards the superficial and deep laminae. The gradient of differentiation of microglia may be related to the growth of the respective regions in the cerebral hemisphere but inherent genetic factors were also considered.

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Year:  1993        PMID: 8226295      PMCID: PMC1259813     

Source DB:  PubMed          Journal:  J Anat        ISSN: 0021-8782            Impact factor:   2.610


  28 in total

1.  Synapses in newborn rat cerebral cortex: a quantitative ultrastructural study.

Authors:  D A Kristt; M E Molliver
Journal:  Brain Res       Date:  1976-05-21       Impact factor: 3.252

2.  The appearance and distribution of microglia in the developing retina of the rat.

Authors:  K W Ashwell; H Holländer; W Streit; J Stone
Journal:  Vis Neurosci       Date:  1989       Impact factor: 3.241

3.  Amoeboid microglial cells in the corpus callosum of neonatal rats.

Authors:  E A Ling; C K Tan
Journal:  Arch Histol Jpn       Date:  1974-03

4.  Cell migrations to the isocortex in the rat.

Authors:  S P Hicks; C J D'Amato
Journal:  Anat Rec       Date:  1968-03

5.  Patterns of vascular sprouting in the postnatal development of the cerebral cortex of the rat.

Authors:  R A Rowan; D S Maxwell
Journal:  Am J Anat       Date:  1981-03

6.  Transitory macrophages in the white matter of the developing visual cortex. II. Development and relations with axonal pathways.

Authors:  G M Innocenti; S Clarke; H Koppel
Journal:  Brain Res       Date:  1983-12       Impact factor: 3.252

7.  New expression of myelomonocytic antigens by microglia and perivascular cells following lethal motor neuron injury.

Authors:  M B Graeber; W J Streit; R Kiefer; S W Schoen; G W Kreutzberg
Journal:  J Neuroimmunol       Date:  1990-05       Impact factor: 3.478

8.  Neuronal differentiation in somatosensory cortex of the rat. I. Relationship to synaptogenesis in the first postnatal week.

Authors:  D A Kristt
Journal:  Brain Res       Date:  1978-07-21       Impact factor: 3.252

9.  Inosine diphosphatase as a histochemical marker of retinal microvasculature, with special reference to transformation of microglia.

Authors:  S Sanyal; A De Ruiter
Journal:  Cell Tissue Res       Date:  1985       Impact factor: 5.249

10.  Immunohistochemical localization of a macrophage-specific antigen in developing mouse retina: phagocytosis of dying neurons and differentiation of microglial cells to form a regular array in the plexiform layers.

Authors:  D A Hume; V H Perry; S Gordon
Journal:  J Cell Biol       Date:  1983-07       Impact factor: 10.539

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  6 in total

1.  A Kv1.5 to Kv1.3 switch in endogenous hippocampal microglia and a role in proliferation.

Authors:  S A Kotecha; L C Schlichter
Journal:  J Neurosci       Date:  1999-12-15       Impact factor: 6.167

2.  Microglia enhance neurogenesis and oligodendrogenesis in the early postnatal subventricular zone.

Authors:  Yukari Shigemoto-Mogami; Kazue Hoshikawa; James E Goldman; Yuko Sekino; Kaoru Sato
Journal:  J Neurosci       Date:  2014-02-05       Impact factor: 6.167

3.  Sex differences in microglial colonization of the developing rat brain.

Authors:  Jaclyn M Schwarz; Paige W Sholar; Staci D Bilbo
Journal:  J Neurochem       Date:  2012-02-09       Impact factor: 5.372

4.  Transcriptome analysis of amoeboid and ramified microglia isolated from the corpus callosum of rat brain.

Authors:  Rangarajan Parakalan; Boran Jiang; Baby Nimmi; Manivannan Janani; Manikandan Jayapal; Jia Lu; Samuel S W Tay; Eng-Ang Ling; S Thameem Dheen
Journal:  BMC Neurosci       Date:  2012-06-14       Impact factor: 3.288

5.  Gestational Exposure to Air Pollution Alters Cortical Volume, Microglial Morphology, and Microglia-Neuron Interactions in a Sex-Specific Manner.

Authors:  Jessica L Bolton; Steven Marinero; Tania Hassanzadeh; Divya Natesan; Dominic Le; Christine Belliveau; S N Mason; Richard L Auten; Staci D Bilbo
Journal:  Front Synaptic Neurosci       Date:  2017-05-31

6.  Reduction of astrogliosis and microgliosis by cerebrospinal fluid shunting in experimental hydrocephalus.

Authors:  Janet M Miller; James P McAllister
Journal:  Cerebrospinal Fluid Res       Date:  2007-06-07
  6 in total

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