Literature DB >> 11337367

Tissue-dependent alteration of protease expression phenotype in murine peritoneal mast cells that were genetically labeled with green fluorescent protein.

T Jippo1, Y M Lee, Y Ge, D K Kim, M Okabe, Y Kitamura.   

Abstract

The changing process of protease expression phenotype was studied after transplantation of peritoneal mast cells (PMCs). To pursue the fate of the transplanted PMCs, we obtained PMCs from WBB6F(1)-c-kit(+)/c-kit(+) mice with a transgene encoding green fluorescent protein (GFP). A large (n = 10(4)) or small (n = 500) number of PMCs was injected into the stomach wall of genetically mast cell-deficient WBB6F(1)-c-kit(W)/c-kit(Wv) mice without the GFP transgene. The original PMCs expressed messenger (m) RNAs of both mast cell carboxypeptidase A (MC-CPA) and mouse mast cell protease (mMCP)-2. The MC-CPA(+)/mMCP-2(+) phenotype did not change in both the muscularis propria and mucosa when 10(4) PMCs were injected. In contrast, when 500 PMCs were injected, the mast cells that developed in the muscularis propria showed MC-CPA(+)/mMCP-2(-) phenotype and those that appeared in the mucosa showed MC-CPA(-)/mMCP-2(+) phenotype. On day 1 after the injection of 500 PMCs, only approximately 20 GFP(+) cells were detected in the muscularis propria and no GFP(+) cells in the mucosa. The proportion of Alcian blue(+) cells decreased until day 7 and increased thereafter. The GFP(+) but Alcian blue(-) cells were considered as degranulated PMCS: The remarkable decrease or degranulation seemed to be necessary for the alteration of protease expression phenotype.

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Year:  2001        PMID: 11337367      PMCID: PMC1891961          DOI: 10.1016/S0002-9440(10)64125-9

Source DB:  PubMed          Journal:  Am J Pathol        ISSN: 0002-9440            Impact factor:   4.307


  28 in total

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Authors:  Y Kitamura
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Authors:  W E Serafin; D S Reynolds; S Rogelj; W S Lane; G A Conder; S S Johnson; K F Austen; R L Stevens
Journal:  J Biol Chem       Date:  1990-01-05       Impact factor: 5.157

3.  Alteration of protease expression phenotype of mouse peritoneal mast cells by changing the microenvironment as demonstrated by in situ hybridization histochemistry.

Authors:  Y M Lee; T Jippo; D K Kim; Y Katsu; K Tsujino; E Morii; H M Kim; S Adachi; Y Nawa; Y Kitamura
Journal:  Am J Pathol       Date:  1998-09       Impact factor: 4.307

4.  Isolation and molecular cloning of mast cell carboxypeptidase A. A novel member of the carboxypeptidase gene family.

Authors:  D S Reynolds; R L Stevens; D S Gurley; W S Lane; K F Austen; W E Serafin
Journal:  J Biol Chem       Date:  1989-11-25       Impact factor: 5.157

5.  Development of mucosal mast cells after injection of a single connective tissue-type mast cell in the stomach mucosa of genetically mast cell-deficient W/Wv mice.

Authors:  S Sonoda; T Sonoda; T Nakano; Y Kanayama; Y Kanakura; H Asai; T Yonezawa; Y Kitamura
Journal:  J Immunol       Date:  1986-08-15       Impact factor: 5.422

6.  Multiple bidirectional alterations of phenotype and changes in proliferative potential during the in vitro and in vivo passage of clonal mast cell populations derived from mouse peritoneal mast cells.

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7.  Different mouse mast cell populations express various combinations of at least six distinct mast cell serine proteases.

Authors:  D S Reynolds; R L Stevens; W S Lane; M H Carr; K F Austen; W E Serafin
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Authors:  T Nakano; T Sonoda; C Hayashi; A Yamatodani; Y Kanayama; T Yamamura; H Asai; T Yonezawa; Y Kitamura; S J Galli
Journal:  J Exp Med       Date:  1985-09-01       Impact factor: 14.307

10.  Phenotypic changes of bone marrow-derived mast cells after intraperitoneal transfer into W/Wv mice that are genetically deficient in mast cells.

Authors:  K Otsu; T Nakano; Y Kanakura; H Asai; H R Katz; K F Austen; R L Stevens; S J Galli; Y Kitamura
Journal:  J Exp Med       Date:  1987-03-01       Impact factor: 14.307

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