Literature DB >> 1572699

Postnatal maturation of mast cell subpopulations in the rat respiratory tract.

L K Wilkes1, C McMenamin, P G Holt.   

Abstract

The distribution and enumeration of mast cell subpopulations within the respiratory tract of a high- and low-Ige responder rat strain was determined during postnatal development. Mast cells were identified in adjacent sections by the alcian blue (AB)/safranin (SAF) staining sequence, or using immunoperoxidase to detect the rat mast cell proteinases I (RMCPI) or II (RMCPII). At birth both mucosal mast cells (MMC) and connective tissue mast cells (CTMC) were represented in very low numbers at distinct locations throughout the respiratory tract. The total number of mast cells increased with age. MMC (AB+/RMCPII+ mast cells) were the predominant phenotype in the epithelium and lamina propria of the trachea and the major conducting airways of the lung in all age groups. In contrast, CTMC (AB+/RPMCPI+ and SAF+/RMCPI+ mast cells) predominated in the submucosa of the trachea and major conducting airways as well as in the parenchyma and visceral pleura of the peripheral lung. Both phenotypes co-exist in similar proportions in peribronchial adventitial tissue and adventitia surrounding large blood vessels in neonates as well as adults. In rats the tracheal epithelium is densely populated by MMC from around the time of weaning (3 weeks) and a small but generalized increase in the number of MMC at all sites within the respiratory tract is noted from this time. This increase in MMC frequency in tissue sections with increasing age is mirrored by the levels of circulating serum RMCPII. The number of bone marrow-derived MMC also increased with increasing age prior to weaning, with a significant drop (P less than 0.01) at 4 weeks of age before returning to the peak numbers in 3-week-old rats. The high-IgE responder Brown Norwegian (BN) rat strain constitutively produces significantly more IgE than the low-IgE responder White albino Glaxo (WAG) strain (P less than 0.001) at all ages studied. In contrast, only minor differences between the number and distribution of mast cells in the two strains were observed.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1572699      PMCID: PMC1384751     

Source DB:  PubMed          Journal:  Immunology        ISSN: 0019-2805            Impact factor:   7.397


  32 in total

Review 1.  Defence against allergic sensitization in the healthy lung: the role of inhalation tolerance.

Authors:  P G Holt; C McMenamin
Journal:  Clin Exp Allergy       Date:  1989-05       Impact factor: 5.018

Review 2.  The mast cells.

Authors:  L Enerbäck; K Norrby
Journal:  Curr Top Pathol       Date:  1989

3.  Mast cell granules cause proliferation of human microvascular endothelial cells.

Authors:  R M Marks; W R Roche; M Czerniecki; R Penny; D S Nelson
Journal:  Lab Invest       Date:  1986-09       Impact factor: 5.662

4.  Two types of human mast cells that have distinct neutral protease compositions.

Authors:  A A Irani; N M Schechter; S S Craig; G DeBlois; L B Schwartz
Journal:  Proc Natl Acad Sci U S A       Date:  1986-06       Impact factor: 11.205

5.  Rat IL-3 stimulates the growth of rat mucosal mast cells in culture.

Authors:  D M Haig; C McMenamin; J Redmond; D Brown; I G Young; S D Cohen; A J Hapel
Journal:  Immunology       Date:  1988-10       Impact factor: 7.397

6.  Granulated intraepithelial lymphocytes: their relationship to mucosal mast cells and globule leucocytes in the rat.

Authors:  J F Huntley; B McGorum; G F Newlands; H R Miller
Journal:  Immunology       Date:  1984-11       Impact factor: 7.397

7.  Concomitant detection of mucosal mast cells and eosinophils in the intestines of normal and Nippostrongylus-immune rats. A re-evaluation of histochemical and immunocytochemical techniques.

Authors:  G F Newlands; J F Huntley; H R Miller
Journal:  Histochemistry       Date:  1984

8.  Mast cell subsets in the rat distinguished immunohistochemically by their content of serine proteinases.

Authors:  S Gibson; H R Miller
Journal:  Immunology       Date:  1986-05       Impact factor: 7.397

9.  Association of maturation of the small intestine at weaning with mucosal mast cell activation in the rat.

Authors:  A G Cummins; G H Munro; H R Miller; A Ferguson
Journal:  Immunol Cell Biol       Date:  1988 Oct-Dec       Impact factor: 5.126

Review 10.  Mucosal mast cells in the rat and in man.

Authors:  L Enerbäck
Journal:  Int Arch Allergy Appl Immunol       Date:  1987
View more
  6 in total

1.  Mast cells mediate hyperoxia-induced airway hyper-reactivity in newborn rats.

Authors:  Eric D Schultz; Erin N Potts; Stanley N Mason; William M Foster; Richard L Auten
Journal:  Pediatr Res       Date:  2010-07       Impact factor: 3.756

2.  Down-regulation of heat shock protein HSP90ab1 in radiation-damaged lung cells other than mast cells.

Authors:  Michael G Haase; Peter Geyer; Guido Fitze; Gustavo B Baretton
Journal:  J Histochem Cytochem       Date:  2014-03-26       Impact factor: 2.479

3.  Protease phenotype of constitutive connective tissue and of induced mucosal mast cells in mice is regulated by the tissue.

Authors:  Wei Xing; K Frank Austen; Michael F Gurish; Tatiana G Jones
Journal:  Proc Natl Acad Sci U S A       Date:  2011-08-08       Impact factor: 11.205

4.  Distribution and characterisation of rat choroidal mast cells.

Authors:  R J Steptoe; P G McMenamin; C McMenamin
Journal:  Br J Ophthalmol       Date:  1994-03       Impact factor: 4.638

5.  Novel phenotype in beagle dogs characterized by skin response to compound 48/80 focusing on skin mast cell degranulation.

Authors:  Mitsuhiro Uchida; Fumi Ito; Toshiyuki Tsuchiya; Yoko Shoji; Toru Kurosawa
Journal:  Exp Anim       Date:  2015-06-09

6.  Expressions of vascular endothelial growth factor receptors, Flk1 and Flt1, in rat skin mast cells during development.

Authors:  Miki Koh; Syunya Noguchi; Mami Araki; Hirotada Otsuka; Makoto Yokosuka; Satoshi Soeta
Journal:  J Vet Med Sci       Date:  2020-04-22       Impact factor: 1.267

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.