Simplified murine multipotent progenitor isolation scheme: Establishing a consensus approach for multipotent progenitor identification

被引:41
作者
Challen, Grant A. [1 ]
Pietras, Eric M. [2 ]
Wallscheid, Nina Cabezas [3 ]
Signer, Robert A. J. [4 ]
机构
[1] Washington Univ, Sch Med, Dept Med, Div Oncol, St Louis, MO 63110 USA
[2] Univ Colorado, Dept Microbiol & Immunol, Div Hematol, Dept Med, Anschutz Med Campus, Aurora, CO USA
[3] Max Planck Inst Immunobiol & Epigenet, Freiburg, Germany
[4] Univ Calif San Diego, Moores Canc Ctr, Dept Med, Div Regenerat Med, La Jolla, CA 92093 USA
关键词
HEMATOPOIETIC STEM-CELLS; SLAM FAMILY MARKERS; BONE-MARROW; LINEAGE COMMITMENT; SELF-RENEWAL; RECONSTITUTION; PURIFICATION; EXPRESSION; SUBSETS; KIT;
D O I
10.1016/j.exphem.2021.09.007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The mouse hematopoietic system has served as a paradigm for analysis of developmental fate decisions in tissue homeostasis and regeneration. However, multiple immunophenotypic definitions of, and sometimes divergent nomenclatures used to classify, murine multipotent progenitors (MPPs) have emerged in the field over time. This has created significant confusion and inconsistency in the hematology field. To facilitate easier comparison of murine MPP phenotypes between research laboratories, a working group of four International Society for Experimental Hematology (ISEH) members with extensive experience studying the functional activities associated with different MPP phenotypic definitions reviewed the current state of the field with the goal of developing a position statement toward a simplified and unified immunophenotypic definition of MPP populations. In November of 2020, this position statement was presented as a webinar to the ISEH community for discussion and feedback. Hence, the Simplified MPP Identification Scheme presented here is the result of curation of existing literature, consultation with leaders in the field, and crowdsourcing from the wider experimental hematology community. Adoption of a unified definition and nomenclature, while still leaving room for individual investigator customization, will benefit scientists at all levels trying to compare these populations between experimental settings. (c) 2021 ISEH - Society for Hematology and Stem Cells. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:55 / 63
页数:9
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