Heterogeneity of the bone marrow niche

被引:73
作者
Yu, Vionnie W. C. [1 ,2 ,3 ,4 ]
Scadden, David T. [1 ,2 ,3 ]
机构
[1] Massachusetts Gen Hosp, Ctr Regenerat Med, Boston, MA 02114 USA
[2] Harvard Univ, Harvard Stem Cell Inst, Cambridge, MA 02138 USA
[3] Harvard Univ, Dept Stem Cell & Regenerat Biol, Cambridge, MA 02138 USA
[4] Novartis Inst BioMed Res, Cambridge, MA USA
基金
美国国家卫生研究院;
关键词
bone marrow niche; hematopoietic stem cell; megakaryocyte; mesenchymal stem cell; mobilization; osteolineage cell; perivascular cells; quiescence; HEMATOPOIETIC STEM-CELL; PROGENITORS; ERYTHROPOIESIS; QUIESCENCE; RELEASE;
D O I
10.1097/MOH.0000000000000265
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Purpose of review The bone marrow niche is increasingly recognized as heterogeneous with specific subtypes of mesenchymal niche cells governing the development or homeostasis of selective parenchymal hematopoietic subsets. The present review outlines recent efforts in dissecting these microniches regulated by unique cell pairings within the bone marrow and provides an overview of how the bone marrow orchestrates multiple facets of hematopoiesis. Recent findings Recent advancement in technologies has significantly improved our understanding of the cellular and molecular constituents that contribute to regulation of hematopoiesis and to maintenance of the hematopoietic stem cells (HSCs). Transgenic mouse models that enable endogenous cell deletion or lineage tracing, coupled with advanced intravital microscopy has identified several mesenchymal cell types, including the osteolineage cells, megakaryocytes, macrophages, perivascular cells, and Schwann cells, to be indispensible regulators of hematopoiesis. These niche cells, when perturbed, each caused very specific hematopoietic consequences including impairment in B-cell maturation, T lineage development, erythropoiesis, and impact different aspects of HSC behavior such as quiescence, mobilization, and response to acute stress signals. Summary The emerging concept is that the bone marrow environment is composed of multiple microniches, each consisting of unique pairing of distinct supportive stromal cells with distinct hematopoietic subtypes to regulate a particular branch of hematopoietic cell process. The bone marrow can be viewed as a carrier with subcompartments tailored to support different hematopoietic activities.
引用
收藏
页码:331 / 338
页数:8
相关论文
共 29 条
[1]
Bone Marrow Macrophages Contribute to Diabetic Stem Cell Mobilopathy by Producing Oncostatin M [J].
Albiero, Mattia ;
Poncina, Nicol ;
Ciciliot, Stefano ;
Cappellari, Roberta ;
Menegazzo, Lisa ;
Ferraro, Francesca ;
Bolego, Chiara ;
Cignarella, Andrea ;
Avogaro, Angelo ;
Fadini, Gian Paolo .
DIABETES, 2015, 64 (08) :2957-2968
[2]
BESSIS M, 1958, Rev Hematol, V13, P8
[3]
Megakaryocytes regulate hematopoietic stem cell quiescence through CXCL4 secretion [J].
Bruns, Ingmar ;
Lucas, Daniel ;
Pinho, Sandra ;
Ahmed, Jalal ;
Lambert, Michele P. ;
Kunisaki, Yuya ;
Scheiermann, Christoph ;
Schiff, Lauren ;
Poncz, Mortimer ;
Bergman, Aviv ;
Frenette, Paul S. .
NATURE MEDICINE, 2014, 20 (11) :1315-1320
[4]
CD169+ macrophages provide a niche promoting erythropoiesis under homeostasis and stress [J].
Chow, Andrew ;
Huggins, Matthew ;
Ahmed, Jalal ;
Hashimoto, Daigo ;
Lucas, Daniel ;
Kunisaki, Yuya ;
Pinho, Sandra ;
Leboeuf, Marylene ;
Noizat, Clara ;
van Rooijen, Nico ;
Tanaka, Masato ;
Zhao, Zhizhuang Joe ;
Bergman, Aviv ;
Merad, Miriam ;
Frenette, Paul S. .
NATURE MEDICINE, 2013, 19 (04) :429-+
[5]
Bone marrow CD169+ macrophages promote the retention of hematopoietic stem and progenitor cells in the mesenchymal stem cell niche [J].
Chow, Andrew ;
Lucas, Daniel ;
Hidalgo, Andres ;
Mendez-Ferrer, Simon ;
Hashimoto, Daigo ;
Scheiermann, Christoph ;
Battista, Michela ;
Leboeuf, Marylene ;
Prophete, Colette ;
van Rooijen, Nico ;
Tanaka, Masato ;
Merad, Miriam ;
Frenette, Paul S. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2011, 208 (02) :261-271
[6]
Haematopoietic stem cells and early lymphoid progenitors occupy distinct bone marrow niches [J].
Ding, Lei ;
Morrison, Sean J. .
NATURE, 2013, 495 (7440) :231-235
[7]
Restoration and reversible expansion of the osteoblastic hematopoietic stem cell niche after marrow radioablation [J].
Dominici, Massimo ;
Rasini, Valeria ;
Bussolari, Rita ;
Chen, Xiaohua ;
Hofmann, Ted J. ;
Spano, Carlotta ;
Bernabei, Daniela ;
Veronesi, Elena ;
Bertoni, Filippo ;
Paolucci, Paolo ;
Conte, PierFranco ;
Horwitz, Edwin M. .
BLOOD, 2009, 114 (11) :2333-2343
[8]
Diabetes Impairs Hematopoietic Stem Cell Mobilization by Altering Niche Function [J].
Ferraro, Francesca ;
Lymperi, Stefania ;
Mendez-Ferrer, Simon ;
Saez, Borja ;
Spencer, Joel A. ;
Yeap, Beow Y. ;
Masselli, Elena ;
Graiani, Gallia ;
Prezioso, Lucia ;
Rizzini, Elisa Lodi ;
Mangoni, Marcellina ;
Rizzoli, Vittorio ;
Sykes, Stephen M. ;
Lin, Charles P. ;
Frenette, Paul S. ;
Quaini, Federico ;
Scadden, David T. .
SCIENCE TRANSLATIONAL MEDICINE, 2011, 3 (104)
[9]
CXCL12 in early mesenchymal progenitors is. required for haematopoietic stem-cell maintenance [J].
Greenbaum, Adam ;
Hsu, Yen-Michael S. ;
Day, Ryan B. ;
Schuettpelz, Laura G. ;
Christopher, Matthew J. ;
Borgerding, Joshua N. ;
Nagasawa, Takashi ;
Link, Daniel C. .
NATURE, 2013, 495 (7440) :227-230
[10]
Megakaryocytes co-localise with hemopoietic stem cells and release cytokines that up-regulate stem cell proliferation [J].
Heazlewood, Shen Y. ;
Neaves, Rebecca J. ;
Williams, Brenda ;
Haylock, David N. ;
Adams, Timothy E. ;
Nilsson, Susan K. .
STEM CELL RESEARCH, 2013, 11 (02) :782-792