Chan Eunice Ching, Bai Yun, Kirshenbaum Arnold S, Fischer Elizabeth R, Simakova Olga, Bandara Geethani, Scott Linda M, Wisch Laura B, Cantave Daly, Carter Melody C, Lewis John C, Noel Pierre, Maric Irina, Gilfillan Alasdair M, Metcalfe Dean D, Wilson Todd M
Mast Cell Biology Section, Laboratory of Allergic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Md.
Research Technologies Section, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Mont.
J Allergy Clin Immunol. 2014 Jul;134(1):178-87. doi: 10.1016/j.jaci.2013.12.1090. Epub 2014 Feb 28.
Mastocytosis associated with germline KIT activating mutations is exceedingly rare. We report the unique clinicopathologic features of a patient with systemic mastocytosis caused by a de novo germline KIT K509I mutation.
We sought to investigate the effect of the germline KIT K509I mutation on human mast cell development and function.
Primary human mast cells derived from CD34(+) peripheral blood progenitors were examined for growth, development, survival, and IgE-mediated activation. In addition, a mast cell transduction system that stably expressed the KIT K509I mutation was established.
KIT K509I biopsied mast cells were round, CD25(-), and well differentiated. KIT K509I progenitors cultured in stem cell factor (SCF) demonstrated a 10-fold expansion compared with progenitors from healthy subjects and developed into mature hypergranular mast cells with enhanced antigen-mediated degranulation. KIT K509I progenitors cultured in the absence of SCF survived but lacked expansion and developed into hypogranular mast cells. A KIT K509I mast cell transduction system revealed SCF-independent survival to be reliant on the preferential splicing of KIT at the adjacent exonic junction.
Germline KIT mutations associated with mastocytosis drive a well-differentiated mast cell phenotype distinct to that of somatic KIT D816V disease, the oncogenic potential of which might be influenced by SCF and selective KIT splicing.
与种系KIT激活突变相关的肥大细胞增多症极为罕见。我们报告了一名由新发种系KIT K509I突变引起的系统性肥大细胞增多症患者独特的临床病理特征。
我们试图研究种系KIT K509I突变对人肥大细胞发育和功能的影响。
对源自CD34(+)外周血祖细胞的原代人肥大细胞进行生长、发育、存活及IgE介导的激活检测。此外,建立了稳定表达KIT K509I突变的肥大细胞转导系统。
KIT K509I活检的肥大细胞呈圆形,CD25(-),且分化良好。与健康受试者的祖细胞相比,在干细胞因子(SCF)中培养的KIT K509I祖细胞扩增了10倍,并发育为成熟的高颗粒肥大细胞,其抗原介导的脱颗粒增强。在无SCF的情况下培养的KIT K509I祖细胞存活,但缺乏扩增,发育为低颗粒肥大细胞。一个KIT K509I肥大细胞转导系统显示,不依赖SCF的存活依赖于KIT在相邻外显子连接处的优先剪接。
与肥大细胞增多症相关的种系KIT突变驱动了一种分化良好的肥大细胞表型,与体细胞KIT D816V疾病不同,其致癌潜力可能受SCF和选择性KIT剪接的影响。