TY - JOUR
T1 - The development of methods for primary mast cells in vitro and ex vivo
T2 - An historical review
AU - Yu, Tianyu
AU - He, Zhigang
AU - Yang, Muqing
AU - Song, Jian
AU - Ma, Cheng
AU - Ma, Sunqiang
AU - Feng, Junlan
AU - Liu, Bin
AU - Wang, Xiaodong
AU - Wei, Zhubo
AU - Li, Jiyu
N1 - Funding Information:
This work was financially supported by a grant from the National Natural Science Foundation of China (Grant no. 81470897, 31741087 ).
Publisher Copyright:
© 2018 Elsevier Inc.
PY - 2018/8/15
Y1 - 2018/8/15
N2 - Mast cells (MCs) are tissue-based stationary effector cells that form the immune system's first-line defense against various challenges. They are developed from the bone marrow-derived progenitors to complete their differentiation and maturation in the tissues where they eventually establish residence. MCs have been implicated in many diseases, such as allergy, parasitic infection, and neoplastic disorders. Immortalized MC lines, such as RBL-2H3, HMC-1, and LAD-2, are useful for investigating the biological functions of MC only to some extents due to the restriction of degranulation evaluation, in vivo injection and other factors. Over the past few decades, technologies for acquiring primarily MCs have been continually optimized, and novel protocols have been proposed. However, no relevant publications have analyzed and summarized these techniques. In this review, the classical approaches for extracting MCs are generalized, and new methods with potential values are introduced. We also evaluate the advantages and applicability of diverse MC models. Since MCs exhibit substantial plasticity and functional diversity due to different origins, it is both necessary and urgent to select a reliable and suitable source of MCs for a particular study.
AB - Mast cells (MCs) are tissue-based stationary effector cells that form the immune system's first-line defense against various challenges. They are developed from the bone marrow-derived progenitors to complete their differentiation and maturation in the tissues where they eventually establish residence. MCs have been implicated in many diseases, such as allergy, parasitic infection, and neoplastic disorders. Immortalized MC lines, such as RBL-2H3, HMC-1, and LAD-2, are useful for investigating the biological functions of MC only to some extents due to the restriction of degranulation evaluation, in vivo injection and other factors. Over the past few decades, technologies for acquiring primarily MCs have been continually optimized, and novel protocols have been proposed. However, no relevant publications have analyzed and summarized these techniques. In this review, the classical approaches for extracting MCs are generalized, and new methods with potential values are introduced. We also evaluate the advantages and applicability of diverse MC models. Since MCs exhibit substantial plasticity and functional diversity due to different origins, it is both necessary and urgent to select a reliable and suitable source of MCs for a particular study.
KW - Bone marrow
KW - Cord blood
KW - IL-3
KW - In vitro culture
KW - Mast cell
KW - SCF
KW - iPS
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U2 - 10.1016/j.yexcr.2018.05.030
DO - 10.1016/j.yexcr.2018.05.030
M3 - Review article
C2 - 29842878
AN - SCOPUS:85049310437
SN - 0014-4827
VL - 369
SP - 179
EP - 186
JO - Experimental Cell Research
JF - Experimental Cell Research
IS - 2
ER -