In Vivo Studies of Human Mast Cells

Author(s):  
Ann M. Dvorak
2010 ◽  
Vol 91 (5) ◽  
pp. 1256-1261 ◽  
Author(s):  
S. Guhl ◽  
R. Franke ◽  
A. Schielke ◽  
R. Johne ◽  
D. H. Kruger ◽  
...  
Keyword(s):  

Blood ◽  
2012 ◽  
Vol 119 (12) ◽  
pp. 2768-2777 ◽  
Author(s):  
Shinsuke Takagi ◽  
Yoriko Saito ◽  
Atsushi Hijikata ◽  
Satoshi Tanaka ◽  
Takashi Watanabe ◽  
...  

Abstract In recent years, advances in the humanized mouse system have led to significantly increased levels of human hematopoietic stem cell (HSC) engraftment. The remaining limitations in human HSC engraftment and function include lymphoid-skewed differentiation and inefficient myeloid development in the recipients. Limited human HSC function may partially be attributed to the inability of the host mouse microenvironment to provide sufficient support to human hematopoiesis. To address this problem, we created membrane-bound human stem cell factor (SCF)/KIT ligand (KL)–expressing NOD/SCID/IL2rgKO (hSCF Tg NSG) mice. hSCF Tg NSG recipients of human HSCs showed higher levels of both human CD45+ cell engraftment and human CD45+CD33+ myeloid development compared with NSG recipients. Expression of hSCF/hKL accelerated the differentiation of the human granulocyte lineage cells in the recipient bone marrow. Human mast cells were identified in bone marrow, spleen, and gastrointestinal tissues of the hSCF Tg NSG recipients. This novel in vivo humanized mouse model demonstrates the essential role of membrane-bound hSCF in human myeloid development. Moreover, the hSCF Tg NSG humanized recipients may facilitate investigation of in vivo differentiation, migration, function, and pathology of human mast cells.


1991 ◽  
Vol 97 (2) ◽  
pp. 305-311 ◽  
Author(s):  
Henry W Lim ◽  
Dan He ◽  
Susana Esquenazi-Behar ◽  
Kim B Yancey ◽  
Nicholas A Soter

1999 ◽  
Vol 83 (5) ◽  
pp. 471-475 ◽  
Author(s):  
Martin K. Church ◽  
Geraldine F. Clough

Blood ◽  
1997 ◽  
Vol 90 (8) ◽  
pp. 2893-2900 ◽  
Author(s):  
Ann M. Dvorak ◽  
John J. Costa ◽  
Ellen S. Morgan ◽  
Rita A. Monahan-Earley ◽  
Stephen J. Galli

AbstractStem cell factor (SCF ) has a major role in hematopoiesis and in the regulation of mast cell development and function. For example, recombinant human SCF (rhSCF ) can induce the development of human mast cells from precursor cells in vitro, stimulate mediator release from human skin mast cells in vitro, and promote both the development and functional activation of human skin mast cells in vivo. In the present study, we used a new ultrastructural enzyme-affinity method, employing diamine oxidase (DAO)-conjugated gold particles (DAO-gold), to detect histamine in skin biopsies obtained from patients with breast carcinomas who were receiving daily subcutaneous (SC) injections of rhSCF in a phase I study of this cytokine. We examined control biopsies obtained at sites remote from rhSCF injection as well as biopsies of rhSCF-injected skin that were obtained within 2 hours and 30 minutes of the SC injection of rhSCF at that site. The rhSCF-injected sites (which clinically exhibited a wheal-and-flare response), but not the control sites, contained mast cells undergoing regulated secretion by granule extrusion. The DAO-gold-affinity method detected histamine in electron-dense granules of mast cells in control and injected skin biopsies; however, the altered matrix of membrane-free, extruded mast cell granules was largely unreactive with DAO-gold. Notably, DAO-gold bound strongly to fibrin deposits and collagen fibers that were adjacent to degranulated mast cells. These findings represent the first morphologic evidence of histamine secretion by classical granule exocytosis in human mast cells in vivo.


1994 ◽  
Vol 94 (5) ◽  
pp. 1974-1980 ◽  
Author(s):  
E Masini ◽  
D Bani ◽  
M Bigazzi ◽  
P F Mannaioni ◽  
T Bani-Sacchi

2021 ◽  
Vol 22 (20) ◽  
pp. 10994
Author(s):  
Kuan-Ming Chiu ◽  
Yen-Ling Hung ◽  
Su-Jane Wang ◽  
Yi-Ju Tsai ◽  
Nan-Lin Wu ◽  
...  

Mast cells play a very important role in skin allergy and inflammation, including atopic dermatitis and psoriasis. In the past, it was found that neferine has anti-inflammatory and anti-aging effects on the skin, but its effect on mast cells has not yet been studied in detail. In this study, we used mast cells (RBL-2H3 cells) and mouse models to study the anti-allergic and inflammatory effects of neferine. First, we found that neferine inhibits the degranulation of mast cells and the expression of cytokines. In addition, we observed that when mast cells were stimulated by A23187/phorbol 12-myristate-13-acetate (PMA), the elevation of intracellular calcium was inhibited by neferine. The phosphorylation of the MAPK/NF-κB pathway is also reduced by pretreatment of neferine. The results of in vivo studies show that neferine can improve the appearance of dermatitis and mast cell infiltration caused by dinitrochlorobenzene (DNCB). Moreover, the expressions of barrier proteins in the skin are also restored. Finally, it was found that neferine can reduce the scratching behavior caused by compound 48/80. Taken together, our results indicate that neferine is a very good anti-allergic and anti-inflammatory natural product. Its effect on mast cells contributes to its pharmacological mechanism.


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