Literature DB >> 2354054

Bromodeoxyuridine labeling studies on the proliferation of intestinal mucosal mast cells in normal and athymic rats.

N Arizono1, T Shiota, M Yamada, Y Matsumoto, H Yoshikawa, S Matsuda, T Tegoshi.   

Abstract

The proliferation of mucosal-type mast cells (MMC) in rat small intestine was studied using a bromodeoxyuridine (BrdU)-labeling method. After 24-h cumulative injections of BrdU into adult SD rats, 3.5% of MMC were labeled, while only 0.3% and 0.1% of mast cells were labeled in back skin and ear respectively. From the results, it was concluded that MMC division occurred more than 10 times as frequently as the division of skin mast cells. Similar results were obtained in athymic adult rats (F344/N Jcl-rnu) in which the number of MMC was similar to that in heterologous animals. Thus, thymic factor(s) or T cells may not have an important role in MMC division in normal states. When SD rats were infected with Nippostrongylus brasiliensis, vigorous proliferation of MMC was brought about 13 to 15 days after infection. At that period, 40% of MMC were labeled by a single injection of BrdU, and 85% of MMC were labeled by 9-h cumulative injections of BrdU, with the result that most MMC rapidly proliferated in the intestinal mucosa during this period. Mitotic figures of MMC were sometimes observed. On the contrary, hyperplasia of MMC was not observed in athymic rats infected with nematodes. Therefore, MMC hyperplasia after nematode infection is dependent on thymic factor or T cells, and its mechanism is different from that of MMC division in normal states, in which thymic factor(s) or T cells are not essential.

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Year:  1990        PMID: 2354054     DOI: 10.1111/j.1699-0463.1990.tb01046.x

Source DB:  PubMed          Journal:  APMIS        ISSN: 0903-4641            Impact factor:   3.205


  6 in total

1.  GPR30 decreases cardiac chymase/angiotensin II by inhibiting local mast cell number.

Authors:  Zhuo Zhao; Hao Wang; Marina Lin; Leanne Groban
Journal:  Biochem Biophys Res Commun       Date:  2015-02-21       Impact factor: 3.575

2.  Dissociation of specific and total IgE antibody responses following repeated low-level infections with Nippostrongylus brasiliensis in rats.

Authors:  M Yamada; R Uchikawa; M Nakazawa; M Oda; N Arizono
Journal:  Clin Exp Immunol       Date:  1993-07       Impact factor: 4.330

3.  Low-level infection with the nematode Nippostrongylus brasiliensis induces significant and sustained specific and non-specific IgE antibody responses in rats.

Authors:  M Yamada; M Nakazawa; I Kamata; N Arizono
Journal:  Immunology       Date:  1992-01       Impact factor: 7.397

4.  The c-kit ligand, stem cell factor, promotes mast cell survival by suppressing apoptosis.

Authors:  A Iemura; M Tsai; A Ando; B K Wershil; S J Galli
Journal:  Am J Pathol       Date:  1994-02       Impact factor: 4.307

5.  Mast cells can amplify airway reactivity and features of chronic inflammation in an asthma model in mice.

Authors:  C M Williams; S J Galli
Journal:  J Exp Med       Date:  2000-08-07       Impact factor: 14.307

6.  The rat c-kit ligand, stem cell factor, induces the development of connective tissue-type and mucosal mast cells in vivo. Analysis by anatomical distribution, histochemistry, and protease phenotype.

Authors:  M Tsai; L S Shih; G F Newlands; T Takeishi; K E Langley; K M Zsebo; H R Miller; E N Geissler; S J Galli
Journal:  J Exp Med       Date:  1991-07-01       Impact factor: 14.307

  6 in total

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