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

被引:42
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
相关论文
共 39 条
[1]   Evidence that hematopoiesis may be a stochastic process in vivo [J].
Abkowitz, JL ;
Catlin, SN ;
Guttorp, P .
NATURE MEDICINE, 1996, 2 (02) :190-197
[2]   Upregulation of flt3 expression within the bone marrow Lin-Sca1+c-kit+ stem cell compartment is accompanied by loss of self-renewal capacity [J].
Adolfsson, J ;
Borge, OJ ;
Bryder, D ;
Theilgaard-Mönch, K ;
Åstrand-Grundström, I ;
Sitnicka, E ;
Sasaki, Y ;
Jacobsen, SEW .
IMMUNITY, 2001, 15 (04) :659-669
[3]   Identification of Flt3+ lympho-myeloid stem cells lacking erythro-megakaryocytic potential:: A revised road map for adult blood lineage commitment [J].
Adolfsson, J ;
Månsson, R ;
Buza-Vidas, N ;
Hultquist, A ;
Liuba, K ;
Jensen, CT ;
Bryder, D ;
Yang, LP ;
Borge, OJ ;
Thoren, LAM ;
Anderson, K ;
Sitnicka, E ;
Sasaki, Y ;
Sigvardsson, M ;
Jacobsen, SEW .
CELL, 2005, 121 (02) :295-306
[4]   A new lymphoid-primed progenitor marked byDach1downregulation identified with single cell multi-omics [J].
Amann-Zalcenstein, Daniela ;
Tian, Luyi ;
Schreuder, Jaring ;
Tomei, Sara ;
Lin, Dawn S. ;
Fairfax, Kirsten A. ;
Bolden, Jessica E. ;
McKenzie, Mark D. ;
Jarratt, Andrew ;
Hilton, Adrienne ;
Jackson, Jacob T. ;
Di Rago, Ladina ;
McCormack, Matthew P. ;
de Graaf, Carolyn A. ;
Stonehouse, Olivia ;
Taoudi, Samir ;
Alexander, Warren S. ;
Nutt, Stephen L. ;
Ritchie, Matthew E. ;
Ng, Ashley P. ;
Naik, Shalin H. .
NATURE IMMUNOLOGY, 2020, 21 (12) :1574-+
[5]   CYTOLOGICAL DEMONSTRATION OF CLONAL NATURE OF SPLEEN COLONIES DERIVED FROM TRANSPLANTED MOUSE MARROW CELLS [J].
BECKER, AJ ;
TILL, JE ;
MCCULLOCH, EA .
NATURE, 1963, 197 (486) :452-&
[6]   Intermediate-Term Hematopoietic Stem Cells with Extended but Time-Limited Reconstitution Potential [J].
Benveniste, Patricia ;
Frelin, Catherine ;
Janmohamed, Salima ;
Barbara, Mary ;
Herrington, Robert ;
Hyam, Deborah ;
Iscove, Norman N. .
CELL STEM CELL, 2010, 6 (01) :48-58
[7]   On the origin of hematopoietic stem cells: Progress and controversy [J].
Boisset, Jean-Charles ;
Robin, Catherine .
STEM CELL RESEARCH, 2012, 8 (01) :1-13
[8]   Identification of Regulatory Networks in HSCs and Their Immediate Progeny via Integrated Proteome, Transcriptome, and DNA Methylome Analysis [J].
Cabezas-Wallscheid, Nina ;
Klimmeck, Daniel ;
Hansson, Jenny ;
Lipka, Daniel B. ;
Reyes, Alejandro ;
Wang, Qi ;
Weichenhan, Dieter ;
Lier, Amelie ;
von Paleske, Lisa ;
Renders, Simon ;
Wuensche, Peer ;
Zeisberger, Petra ;
Brocks, David ;
Gu, Lei ;
Herrmann, Carl ;
Haas, Simon ;
Essers, Marieke A. G. ;
Brors, Benedikt ;
Eils, Roland ;
Huber, Wolfgang ;
Milsom, Michael D. ;
Plass, Christoph ;
Krijgsveld, Jeroen ;
Trumpp, Andreas .
CELL STEM CELL, 2014, 15 (04) :507-522
[9]   Flk-2 is a marker in hematopoietic stem cell differentiation: A simple method to isolate long-term stem cells [J].
Christensen, JL ;
Weissman, IL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (25) :14541-14546
[10]   Hematopoietic stem cells need two signals to prevent apoptosis; BCL-2 can provide one of these, Kitl/c-Kit signaling the other [J].
Domen, J ;
Weissman, IL .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (12) :1707-1718