|
|
Previous Article | Table of Contents | Next Article 
Phorbol 12-myristate 13-acetate-induced development of functionally active
mast cells in W/Wv but not Sl/Sld genetically mast cell- deficient mice
JR Gordon and SJ Galli
Department of Pathology, Beth Israel Hospital, Boston, MA 02215.
The normal skin and other tissues of adult genetically mast cell- deficient
WBB6F1-W/Wv or WCB6F1-Sl/Sld mice contain less than 1.0% the number of mast
cells present in the corresponding tissues of the congenic normal (+/+)
mice. We previously reported that mature dermal mast cells developed
locally in the skin of W/Wv, but not Sl/Sld, mice at sites of chronic
idiopathic dermatitis. We now report that the repeated application of
phorbol 12-myristate 13-acetate (PMA) to the ear skin of either W/Wv or +/+
mice induces both dermatitis and a striking and dose-dependent increase in
the number of dermal mast cells. The number of dermal mast cells at sites
treated for 6 weeks with 5 micrograms PMA, three times per week, was 39 +/-
7/mm2 and 305 +/- 34/mm2 for W/Wv and +/+ mice, respectively; the
corresponding values for vehicle-treated skin were 1.5 +/- 1.0/mm2 and 145
+/- 8/mm2, respectively. The PMA-induced dermal mast cells in W/Wv mice
appeared mature by morphology, stained with the heparin-binding fluorescent
dye, berberine sulfate, and were competent to express IgE-dependent passive
cutaneous anaphylaxis responses. The development of mast cells was a local,
not systemic, effect of PMA treatment. PMA treatment also induced
dermatitis in both WCB6F1-Sl/Sld and +/+ mice, but was associated with
increased numbers of dermal mast cells only in the WCB6F1(-)+/+ mice. PMA
treatment had no detectable effect on the ability of bone marrow-derived
cultured mast cells to survive in the skin of Sl/Sld mice. These findings
establish a convenient model system for analyzing factors associated with
the development of endogenous populations of mast cells in genetically mast
cell-deficient W/Wv mice.
Volume 75,
Issue 8,
pp. 1637-1645,
04/15/1990
Copyright © 1990 by The American Society of Hematology

CiteULike Connotea Del.icio.us Digg Reddit Technorati What's this?
This article has been cited by other articles:

|
 |

|
 |
 
G. P. Katsoulotos, M. Qi, J. C. Qi, K. Tanaka, W. E. Hughes, T. J. Molloy, R. Adachi, R. L. Stevens, and S. A. Krilis
The Diacylglycerol-dependent Translocation of Ras Guanine Nucleotide-releasing Protein 4 inside a Human Mast Cell Line Results in Substantial Phenotypic Changes, Including Expression of Interleukin 13 Receptor {alpha}2
J. Biol. Chem.,
January 18, 2008;
283(3):
1610 - 1621.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
C. Waskow, S. Bartels, S. M. Schlenner, C. Costa, and H.-R. Rodewald
Kit is essential for PMA-inflammation-induced mast-cell accumulation in the skin
Blood,
June 15, 2007;
109(12):
5363 - 5370.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
Y. Yang, L. Li, G. W. Wong, S. A. Krilis, M. S. Madhusudhan, A. Sali, and R. L. Stevens
RasGRP4, a New Mast Cell-restricted Ras Guanine Nucleotide-releasing Protein with Calcium- and Diacylglycerol-binding Motifs. IDENTIFICATION OF DEFECTIVE VARIANTS OF THIS SIGNALING PROTEIN IN ASTHMA, MASTOCYTOSIS, AND MAST CELL LEUKEMIA PATIENTS AND DEMONSTRATION OF THE IMPORTANCE OF RasGRP4 IN MAST CELL DEVELOPMENT AND FUNCTION
J. Biol. Chem.,
July 5, 2002;
277(28):
25756 - 25774.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. F. Gurish, H. Tao, J. P. Abonia, A. Arya, D. S. Friend, C. M. Parker, and K. F. Austen
Intestinal Mast Cell Progenitors Require CD49d{beta}7 ({alpha}4{beta}7 Integrin) for Tissue-specific Homing
J. Exp. Med.,
October 29, 2001;
194(9):
1243 - 1252.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|
|