Literature DB >> 3446660

Origin and fate of neural macrophages in a stab wound of the brain of the young rat.

C Kaur1, E A Ling, W C Wong.   

Abstract

Colloidal carbon was injected intravenously into young rats to label circulating monocytes before making a stab wound in the brain. The rats were killed 3-16 days after the stab wound. Demonstration of non-specific esterase, thiamine pyrophosphatase and 5'-nucleotidase was carried out on the carbon-labelled macrophages at the site of lesion at various survival times. In rats killed 3-5 days after the injury numerous carbon-labelled macrophages were present in the needle passage as well as in the marginal area of the lesion and they showed a positive reaction for non-specific esterase. The reaction of the enzyme was found in some of the dense bodies in the form of punctate precipitates. The reaction for thiamine pyrophosphatase was seen in the Golgi saccules as well as on the plasma membrane, although in the latter the reaction was weaker. Intense reaction for 5'-nucleotidase was localised over the plasma membrane as well as over the dense bodies. The carbon-labelled macrophages displaying the activities of the above enzymes in the 3-5 days postoperative group were of the round type. However, in the 8-16 postoperative days animals, the cells were either oval or had assumed an elongated outline resembling the microglial cells seen in the tissue taken from the normal side. It is concluded that circulating monocytes are a main source of brain macrophage in traumatic brain lesions. In the healing process of the wound some of the cells regress to become microglial cells as shown by the presence of the carbon particles as well as non-specific esterase, thiamine pyrophosphatase and 5'-nucleotidase activity in the various stages of structural transformation.

Entities:  

Mesh:

Year:  1987        PMID: 3446660      PMCID: PMC1261847     

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


  54 in total

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Authors:  D A Fernando
Journal:  Brain Res       Date:  1971-04-02       Impact factor: 3.252

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

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Journal:  Arch Histol Jpn       Date:  1974-03

3.  Esterases in human leukocytes.

Authors:  C Y Li; K W Lam; L T Yam
Journal:  J Histochem Cytochem       Date:  1973-01       Impact factor: 2.479

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Authors:  G W Kreutzberg
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Authors:  L Rozenszajn; M Leibovich; D Shoham; J Epstein
Journal:  Br J Haematol       Date:  1968-06       Impact factor: 6.998

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.  Light and electron microscopic demonstration of non-specific esterase in amoeboid microglial cells in the corpus callosum in postnatal rats: a cytochemical link to monocytes.

Authors:  E A Ling; C Kaur; W C Wong
Journal:  J Anat       Date:  1982-09       Impact factor: 2.610

8.  5'-Nucleotidase of microglial cells in the facial nucleus during axonal reaction.

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Journal:  J Neurocytol       Date:  1978-10

9.  Thiaminepyrophosphatase activity in the plasma membrane of microglia.

Authors:  Y Murabe; Y Sano
Journal:  Histochemistry       Date:  1981

10.  Non-specific esterase activity in reactive cells in injured nervous tissue labeled with 3H-thymidine or 125iododeoxyuridine injected before injury.

Authors:  R L Schelper; E K Adrian
Journal:  J Comp Neurol       Date:  1980-12-15       Impact factor: 3.215

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  11 in total

1.  Hematopoietic CC-chemokine receptor 2 (CCR2) competent cells are protective for the cognitive impairments and amyloid pathology in a transgenic mouse model of Alzheimer's disease.

Authors:  Gaëlle Naert; Serge Rivest
Journal:  Mol Med       Date:  2012-03-30       Impact factor: 6.354

2.  The fractalkine receptor but not CCR2 is present on microglia from embryonic development throughout adulthood.

Authors:  Makiko Mizutani; Paula A Pino; Noah Saederup; Israel F Charo; Richard M Ransohoff; Astrid E Cardona
Journal:  J Immunol       Date:  2011-11-11       Impact factor: 5.422

3.  Response of intraventricular macrophages to crotoxin-coated microcarrier beads injected into the lateral ventricle of postnatal rats.

Authors:  C Kaur; E A Ling; P Gopalakrishnakone; W C Wong
Journal:  J Anat       Date:  1990-02       Impact factor: 2.610

Review 4.  Mechanisms and significance of microglia-axon interactions in physiological and pathophysiological conditions.

Authors:  Yuki Fujita; Toshihide Yamashita
Journal:  Cell Mol Life Sci       Date:  2021-01-28       Impact factor: 9.261

5.  Ultrastructural organization of the medial preoptic region of the hypothalamus and its alterations under the influence of pyrogens.

Authors:  L I Archakova; E M Belyavskii; V N Gurin
Journal:  Neurosci Behav Physiol       Date:  1990 Mar-Apr

6.  Intracerebral inflammatory response to experimental brain contusion.

Authors:  S Holmin; T Mathiesen; J Shetye; P Biberfeld
Journal:  Acta Neurochir (Wien)       Date:  1995       Impact factor: 2.216

7.  Infiltration of carbon-labelled monocytes into the dorsal motor nucleus following an intraneural injection of ricinus communis agglutinin-60 into the vagus nerve in rats.

Authors:  E A Ling; S K Leong
Journal:  J Anat       Date:  1988-08       Impact factor: 2.610

8.  Induction of cytosolic NADPH-diaphorase/nitric oxide synthase in reactive microglia/macrophages after quinolinic acid lesions in the rat striatum: an electron and light microscopical study.

Authors:  J Calka; G Wolf; W Schmidt
Journal:  Histochem Cell Biol       Date:  1996-01       Impact factor: 4.304

9.  CXCL1 contributes to β-amyloid-induced transendothelial migration of monocytes in Alzheimer's disease.

Authors:  Ke Zhang; Li Tian; Li Liu; Yu Feng; Yan-Bin Dong; Bo Li; De-Shu Shang; Wen-Gang Fang; Yun-Peng Cao; Yu-Hua Chen
Journal:  PLoS One       Date:  2013-08-14       Impact factor: 3.240

10.  Characterization of brain-infiltrating mononuclear cells during infection with mouse hepatitis virus strain JHM.

Authors:  J S Williamson; K C Sykes; S A Stohlman
Journal:  J Neuroimmunol       Date:  1991-06       Impact factor: 3.478

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