生物
斑马鱼
脱颗粒
免疫球蛋白E
类胰蛋白酶
受体
分子生物学
先天免疫系统
免疫学
抗体
免疫系统
肥大细胞
细胞生物学
生物化学
基因
作者
Sahar I. Da’as,Evelyn M. Teh,J. Tristan Dobson,Gheyath K. Nasrallah,Eileen McBride,Hao Wang,Donna Neuberg,Jean S. Marshall,Tong‐Jun Lin,Jason N. Berman
标识
DOI:10.1016/j.dci.2010.09.001
摘要
We previously identified a zebrafish mast cell (MC) lineage and now aim to determine if these cells function analogously in innate and adaptive immunity like their mammalian counterparts. Intraperitoneal (IP) injection of compound 48/80 or live Aeromonas salmonicida resulted in significant MC degranulation evident histologically and by increased plasma tryptase compared with saline-injected controls (p = 0.0006, 0.005, respectively). Pre-treatment with ketotifen abrogated these responses (p = 0.0004, 0.005, respectively). Cross-reactivity was observed in zebrafish to anti-human high-affinity IgE receptor gamma (FcɛRIγ) and IgE heavy chain-directed antibodies. Whole mount in situ hybridization on 7-day embryos demonstrated co-localization of cpa5, a MC-specific marker, with myd88, a toll-like receptor adaptor, and zebrafish FcɛRI subunit homologs. Zebrafish injected IP with matched dinitrophenyl-sensitized mouse (anti-DNP) IgE and DNP-BSA or trinitrophenyl-sensitized mouse (anti-TNP) IgE and TNP-BSA demonstrated increased plasma tryptase compared with mismatched controls (p = 0.03, 0.010, respectively). These results confirm functional conservation and validate the zebrafish model as an in vivo screening tool for novel MC modulating agents.
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