The DOI matches its Crossref record; 17 of the 17 references it cites were found in a registry or an index.
Redox regulation of stem/progenitor cells and bone marrow niche
Open accessAbstract
Bone marrow (BM)-derived stem and progenitor cell functions including self-renewal, differentiation, survival, migration, proliferation and mobilization are regulated by unique cell-intrinsic signals and -extrinsic signals provided by their microenvironment, also termed the ‘niche’. Reactive oxygen species (ROS), especially hydrogen peroxide (H2O2), play important roles in regulating stem and progenitor cell function in various physiologic and pathologic responses. The low level of H2O2 in quiescent hematopoietic stem cells (HSCs) contributes to maintain their stemness, whereas a higher level of H2O2 within HSCs or their niche promotes differentiation, proliferation, migration, and survival of HSCs or stem/progenitor cells. Major sources of ROS are NADPH oxidase and mitochondria. In response to ischemic injury, ROS derived from NADPH oxidase are increased in the BM microenvironment, which is required for hypoxia and HIF1α expression and expansion throughout the BM. This, in turn, promotes progenitor cell expansion and mobilization from BM, leading to reparative neovascularization and tissue repair. In pathophysiological states such as aging, atherosclerosis, heart failure, hypertension and diabetes, excess amounts of ROS create an inflammatory and oxidative microenvironment, which induces cell damage and apoptosis of stem and progenitor cells. Understanding the molecular mechanisms of how ROS regulate the functions of stem and progenitor cells and their niche in physiological and pathological conditions will lead to the development of novel therapeutic strategies.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Isolation of Putative Progenitor Endothelial Cells for Angiogenesis
Asahara, T., Murohara, T., Sullivan, A., Silver, M., van der Zee, R., Li, T., Witzenbichler, B., Schatteman, G., & Isner, J. M. (1997) · Science · doi:10.1126/science.275.5302.964 · Cited by 8,725
Circulating endothelial progenitor cells, vascular function, and cardiovascular risk
Hill, J. M., Zalos, G., Halcox, J. P. J., Schenke, W. H., Waclawiw, M. A., Quyyumi, A. A., & Finkel, T. (2003) · New England Journal of Medicine · doi:10.1056/nejmoa022287 · Cited by 3,423
Signal transduction by reactive oxygen species
Finkel, T. (2011) · Journal of Cell Biology · doi:10.1083/jcb.201102095 · Cited by 2,322 · cited 1×
“In contrast, ROS, especially H2O2, at physiological levels function as signaling molecules to mediate various biological responses such as cell proliferation, migration, survival, differentiation and gene expression [24-27].”
BackgroundFoxOs Are Critical Mediators of Hematopoietic Stem Cell Resistance to Physiologic Oxidative Stress
Tothova, Z., Kollipara, R., Huntly, B. J., Lee, B. H., Castrillon, D. H., Cullen, D. E., McDowell, E. P., Lazo-Kallanian, S., Williams, I. R., Sears, C., et al. (2007) · Cell · doi:10.1016/j.cell.2007.01.003 · Cited by 1,562
Topology of superoxide production from different sites in the mitochondrial electron transport chain
St-Pierre, J., Buckingham, J. A., Roebuck, S. J., & Brand, M. D. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m207217200 · Cited by 1,545
Reactive oxygen species act through p38 MAPK to limit the lifespan of hematopoietic stem cells
Ito, K., Hirao, A., Arai, F., Takubo, K., Matsuoka, S., Miyamoto, K., Ohmura, M., Naka, K., Hosokawa, K., Ikeda, Y., et al. (2006) · Nature Medicine · doi:10.1038/nm1388 · Cited by 1,362
Regulation of oxidative stress by ATM is required for self-renewal of haematopoietic stem cells
Ito, K., Hirao, A., Arai, F., Matsuoka, S., Takubo, K., Hamaguchi, I., Nomiyama, K., Hosokawa, K., Sakurada, K., Nakagata, N., et al. (2004) · Nature · doi:10.1038/nature02989 · Cited by 1,175 · cited 6×
“As described above, mice lacking essential components of the regulatory system that maintains ROS within the physiological levels, show accelerated HSCs senescence and progressive BM failure [17,20].”
BackgroundInfluentialSimsek, T., Kocabas, F., Zheng, J., DeBerardinis, R. J., Mahmoud, A. I., Olson, E. N., Schneider, J. W., Zhang, C. C., & Sadek, H. A. (2010) · Cell Stem Cell · doi:10.1016/j.stem.2010.07.011 · Cited by 1,101
Metabolic Regulation of Hematopoietic Stem Cells in the Hypoxic Niche
Suda, T., Takubo, K., & Semenza, G. L. (2011) · Cell Stem Cell · doi:10.1016/j.stem.2011.09.010 · Cited by 844
Chen, C., Liu, Y., Liu, R., Ikenoue, T., Guan, K.-L., Liu, Y., & Zheng, P. (2008) · The Journal of Experimental Medicine · doi:10.1084/jem.20081297 · Cited by 682
Research works printed but not linked: 172
- Rafii, 2003, Angiogenic factors reconstitute hematopoiesis by recruiting stem cells from bone marrow microenvironment, Ann. N. Y. Acad. Sci, 996, 49, 10.1111/j.1749-6632.2003.tb03232.x · DOI
- Tepper, 2002, Human endothelial progenitor cells from type II diabetics exhibit impaired proliferation, adhesion, and incorporation into vascular structures, Circulation, 106, 2781, 10.1161/01.CIR.0000039526.42991.93 · DOI · Paper page
- Jin, 2006, Cytokine-mediated deployment of SDF-1 induces revascularization through recruitment of CXCR4+ hemangiocytes, Nat. Med, 12, 557, 10.1038/nm1400 · DOI · Paper page
- Goldie, 2008, Embryonic vasculogenesis and hematopoietic specification, Organogenesis, 4, 257, 10.4161/org.4.4.7416 · DOI
- Zape, 2011, Hemogenic endothelium: origins, regulation, and implications for vascular biology, Semin. Cell Dev. Biol., 22, 1036, 10.1016/j.semcdb.2011.10.003 · DOI
- Chao, 2010, Hemato-vascular origins of endothelial progenitor cells?, Microvasc. Res, 79, 169, 10.1016/j.mvr.2010.02.003 · DOI
- Kiel, 2008, Uncertainty in the niches that maintain haematopoietic stem cells, Nat. Rev. Immunol, 8, 290, 10.1038/nri2279 · DOI · Paper page
- Renstrom, 2010, How the niche regulates hematopoietic stem cells, Chem. Biol. Interact., 184, 7, 10.1016/j.cbi.2009.11.012 · DOI
- Takubo, 2008, Stem cell defects in ATM-deficient undifferentiated spermatogonia through DNA damage-induced cell-cycle arrest, Cell Stem Cell, 2, 170, 10.1016/j.stem.2007.10.023 · DOI
- Levesque, 2011, Hierarchy of immature hematopoietic cells related to blood flow and niche, Curr. Opin. Hematol, 18, 220, 10.1097/MOH.0b013e3283475fe7 · DOI
- Weber, 2010, Notch signaling and the bone marrow hematopoietic stem cell niche, Bone, 46, 281, 10.1016/j.bone.2009.08.007 · DOI
- Lilly, 2011, The haematopoietic stem cell niche: new insights into the mechanisms regulating haematopoietic stem cell behaviour, Stem Cells Int., 2011, 274564, 10.4061/2011/274564 · DOI
- Sardina, 2012, Reactive oxygen species: are they important for haematopoiesis?, Crit. Rev. Oncol. Hematol, 81, 257, 10.1016/j.critrevonc.2011.03.005 · DOI
- Eliasson, 2010, Hypoxia mediates low cell-cycle activity and increases the proportion of long-term-reconstituting hematopoietic stem cells during in vitro culture, Exp. Hematol, 38, 301, 10.1016/j.exphem.2010.01.005 · DOI · Paper page
- Case, 2008, Oxidative stress impairs endothelial progenitor cell function, Antioxid. Redox Signaling, 10, 1895, 10.1089/ars.2008.2118 · DOI
- Kobayashi, 2012, Regulation of reactive oxygen species in stem cells and cancer stem cells, J. Cell. Physiol, 227, 421, 10.1002/jcp.22764 · DOI · Paper page
- Jang, 2007, A low level of reactive oxygen species selects for primitive hematopoietic stem cells that may reside in the low-oxygenic niche, Blood, 110, 3056, 10.1182/blood-2007-05-087759 · DOI · Paper page
- Naka, 2008, Regulation of reactive oxygen species and genomic stability in hematopoietic stem cells, Antioxid. Redox Signaling, 10, 1883, 10.1089/ars.2008.2114 · DOI · Paper page
- Urao, 2012, NADPH oxidase 2 regulates bone marrow microenvironment following hindlimb ischemia: role in reparative mobilization of progenitor cells, Stem Cells, 30, 923, 10.1002/stem.1048 · DOI
- Griendling, 2000, NAD(P)H oxidase: role in cardiovascular biology and disease, Circ. Res, 86, 494, 10.1161/01.RES.86.5.494 · DOI · Paper page
- Rhee, 2000, Hydrogen peroxide: a key messenger that modulates protein phosphorylation through cysteine oxidation, Sci. STKE, 2000, pe1, 10.1126/stke.2000.53.pe1 · DOI · Paper page
- Ushio-Fukai, 2006, Redox signaling in angiogenesis: role of NADPH oxidase, Cardiovasc. Res., 71, 226, 10.1016/j.cardiores.2006.04.015 · DOI · Paper page
- Nathan, 2010, SnapShot: reactive oxygen intermediates (ROI), Cell, 140, 951, 10.1016/j.cell.2010.03.008 · DOI · Paper page
- Fukai, 2011, Superoxide dismutases: role in redox signaling, vascular function, and diseases, Antioxid. Redox Signaling, 15, 1583, 10.1089/ars.2011.3999 · DOI · Paper page
- Michiels, 1994, Importance of Se-glutathione peroxidase, catalase, and Cu/Zn-SOD for cell survival against oxidative stress, Free Radic. Biol. Med, 17, 235, 10.1016/0891-5849(94)90079-5 · DOI · Paper page
- Dernbach, 2004, Antioxidative stress-associated genes in circulating progenitor cells: evidence for enhanced resistance against oxidative stress, Blood, 104, 3591, 10.1182/blood-2003-12-4103 · DOI · Paper page
- Lassegue, 2012, Biochemistry, physiology, and pathophysiology of NADPH oxidases in the cardiovascular system, Circ. Res., 110, 1364, 10.1161/CIRCRESAHA.111.243972 · DOI · Paper page
- Ushio-Fukai, 2009, Novel role of NADPH oxidase in angiogenesis and stem/progenitor cell function, Antioxid. Redox Signaling, 11, 2517, 10.1089/ars.2009.2582 · DOI
- Ushio-Fukai, 2009, Compartmentalization of redox signaling through NADPH oxidase-derived ROS, Antioxid. Redox Signaling, 11, 1289, 10.1089/ars.2008.2333 · DOI · Paper page
- Jiang, 2011, NADPH oxidase-mediated redox signaling: roles in cellular stress response, stress tolerance, and tissue repair, Pharmacol. Rev., 63, 218, 10.1124/pr.110.002980 · DOI · Paper page
- Diaz, 2012, Redox signaling at invasive microdomains in cancer cells, Free Radic. Biol. Med, 52, 247, 10.1016/j.freeradbiomed.2011.09.016 · DOI
- Coso, 2012, NADPH oxidases as regulators of tumor angiogenesis: current and emerging concepts, Antioxid. Redox Signaling, 16, 1229, 10.1089/ars.2011.4489 · DOI
- Sareila, 2011, NOX2 complex-derived ROS as immune regulators, Antioxid. Redox Signaling, 15, 2197, 10.1089/ars.2010.3635 · DOI · Paper page
- Lam, 2010, The many roles of NOX2 NADPH oxidase-derived ROS in immunity, Semin. Immunopathol, 32, 415, 10.1007/s00281-010-0221-0 · DOI · Paper page
- Fiorentini, 2004, Contribution of reactive oxygen species to the regulation of Glut1 in two hemopoietic cell lines differing in cytokine sensitivity, Free Radic. Biol. Med, 37, 1402, 10.1016/j.freeradbiomed.2004.07.022 · DOI
- Urao, 2008, Role of nox2-based NADPH oxidase in bone marrow and progenitor cell function involved in neovascularization induced by hindlimb ischemia, Circ. Res, 103, 212, 10.1161/CIRCRESAHA.108.176230 · DOI · Paper page
- Zhang, 2010, NADPH oxidase-4 mediates protection against chronic load-induced stress in mouse hearts by enhancing angiogenesis, Proc. Natl. Acad. Sci. USA, 107, 18121, 10.1073/pnas.1009700107 · DOI · Paper page
- Fadini, 2006, Number and function of endothelial progenitor cells as a marker of severity for diabetic vasculopathy, Arterioscler. Thromb. Vasc. Biol, 26, 2140, 10.1161/01.ATV.0000237750.44469.88 · DOI · Paper page
- Dikalov, 2011, Cross talk between mitochondria and NADPH oxidases, Free Radic. Biol. Med., 51, 1289, 10.1016/j.freeradbiomed.2011.06.033 · DOI · Paper page
- Lee, 2006, Link between mitochondria and NADPH oxidase 1 isozyme for the sustained production of reactive oxygen species and cell death, J. Biol. Chem, 281, 36228, 10.1074/jbc.M606702200 · DOI · Paper page
- Miller, 2009, Molecular regulation of tumor angiogenesis and perfusion via redox signaling, Chem. Rev, 109, 3099, 10.1021/cr8005125 · DOI
- Parmar, 2007, Distribution of hematopoietic stem cells in the bone marrow according to regional hypoxia, Proc. Natl. Acad. Sci. USA, 104, 5431, 10.1073/pnas.0701152104 · DOI · Paper page
- Owusu-Ansah, 2009, Reactive oxygen species prime Drosophila haematopoietic progenitors for differentiation, Nature, 461, 537, 10.1038/nature08313 · DOI · Paper page
- Sattler, 1999, Hematopoietic growth factors signal through the formation of reactive oxygen species, Blood, 93, 2928, 10.1182/blood.V93.9.2928.409k25_2928_2935 · DOI
- Tesio, 2011, Enhanced c-Met activity promotes G-CSF-induced mobilization of hematopoietic progenitor cells via ROS signaling, Blood, 117, 419, 10.1182/blood-2009-06-230359 · DOI
- Milovanova, 2009, Hyperbaric oxygen stimulates vasculogenic stem cell growth and differentiation in vivo, J. Appl. Physiol, 106, 711, 10.1152/japplphysiol.91054.2008 · DOI
- Wang, 2011, Inhibition of p38 mitogen-activated protein kinase promotes ex vivo hematopoietic stem cell expansion, Stem Cells Dev, 20, 1143, 10.1089/scd.2010.0413 · DOI
- Yun, 2009, Redox-dependent mechanisms in coronary collateral growth: the “redox window” hypothesis, Antioxid. Redox Signaling, 11, 1961, 10.1089/ars.2009.2476 · DOI
- Terskikh, 2003, Gene expression analysis of purified hematopoietic stem cells and committed progenitors, Blood, 102, 94, 10.1182/blood-2002-08-2509 · DOI · Paper page
- Piccoli, 2007, Bone-marrow derived hematopoietic stem/progenitor cells express multiple isoforms of NADPH oxidase and produce constitutively reactive oxygen species, Biochem. Biophys. Res. Commun, 353, 965, 10.1016/j.bbrc.2006.12.148 · DOI
- Frassanito, 2008, Topological organization of NADPH-oxidase in haematopoietic stem cell membrane: preliminary study by fluorescence near-field optical microscopy, J. Microsc, 229, 517, 10.1111/j.1365-2818.2008.01937.x · DOI
- Schroder, 2009, NADPH oxidase Nox2 is required for hypoxia-induced mobilization of endothelial progenitor cells, Circ. Res, 105, 537, 10.1161/CIRCRESAHA.109.205138 · DOI
- Schroder, 2011, Hepatocyte growth factor induces a proangiogenic phenotype and mobilizes endothelial progenitor cells by activating Nox2, Antioxid. Redox Signaling, 15, 915, 10.1089/ars.2010.3533 · doi:10.1089/ars.2010.3533
- Sauer, 2000, Role of reactive oxygen species and phosphatidylinositol 3-kinase in cardiomyocyte differentiation of embryonic stem cells, FEBS Lett, 476, 218, 10.1016/S0014-5793(00)01747-6 · DOI · Paper page
- Sauer, 2005, Redox control of angiogenic factors and CD31-positive vessel-like structures in mouse embryonic stem cells after direct current electrical field stimulation, Exp. Cell Res, 304, 380, 10.1016/j.yexcr.2004.11.026 · DOI
- Schmelter, 2006, Embryonic stem cells utilize reactive oxygen species as transducers of mechanical strain-induced cardiovascular differentiation, FASEB J., 20, 1182, 10.1096/fj.05-4723fje · DOI · Paper page
- Xiao, 2009, Embryonic stem cell differentiation into smooth muscle cells is mediated by Nox4-produced H2O2, Am. J. Physiol. Cell Physiol, 296, C711, 10.1152/ajpcell.00442.2008 · DOI · Paper page
- Saretzki, 2004, Stress defense in murine embryonic stem cells is superior to that of various differentiated murine cells, Stem Cells, 22, 962, 10.1634/stemcells.22-6-962 · DOI · Paper page
- Buggisch, 2007, Stimulation of ES-cell-derived cardiomyogenesis and neonatal cardiac cell proliferation by reactive oxygen species and NADPH oxidase, J. Cell Sci, 120, 885, 10.1242/jcs.03386 · DOI · Paper page
- Sauer, 1999, Effects of electrical fields on cardiomyocyte differentiation of embryonic stem cells, J. Cell. Biochem, 75, 710, 10.1002/(SICI)1097-4644(19991215)75:4<710::AID-JCB16>3.0.CO;2-Z · DOI · Paper page
- Serena, 2009, Electrical stimulation of human embryonic stem cells: cardiac differentiation and the generation of reactive oxygen species, Exp. Cell Res, 315, 3611, 10.1016/j.yexcr.2009.08.015 · DOI · Paper page
- Sauer, 2004, Involvement of reactive oxygen species in cardiotrophin-1-induced proliferation of cardiomyocytes differentiated from murine embryonic stem cells, Exp. Cell Res, 294, 313, 10.1016/j.yexcr.2003.10.032 · DOI
- Lange, 2009, Platelet-derived growth factor BB stimulates vasculogenesis of embryonic stem cell-derived endothelial cells by calcium-mediated generation of reactive oxygen species, Cardiovasc. Res, 81, 159, 10.1093/cvr/cvn258 · DOI
- Sharifpanah, 2008, Peroxisome proliferator-activated receptor alpha agonists enhance cardiomyogenesis of mouse ES cells by utilization of a reactive oxygen species-dependent mechanism, Stem Cells, 26, 64, 10.1634/stemcells.2007-0532 · DOI
- Li, 2006, The NADPH oxidase NOX4 drives cardiac differentiation: role in regulating cardiac transcription factors and MAP kinase activation, Mol. Biol. Cell, 17, 3978, 10.1091/mbc.e05-06-0532 · DOI · Paper page
- Hannig, 2010, Control of leucocyte differentiation from embryonic stem cells upon vasculogenesis and confrontation with tumour tissue, J. Cell Mol. Med, 14, 303, 10.1111/j.1582-4934.2008.00424.x · DOI
- Storz, 2011, Forkhead homeobox type O transcription factors in the responses to oxidative stress, Antioxid. Redox Signaling, 14, 593, 10.1089/ars.2010.3405 · DOI · Paper page
- Miyamoto, 2007, Foxo3a is essential for maintenance of the hematopoietic stem cell pool, Cell Stem Cell, 1, 101, 10.1016/j.stem.2007.02.001 · DOI · Paper page
- Miyamoto, 2008, FoxO3a regulates hematopoietic homeostasis through a negative feedback pathway in conditions of stress or aging, Blood, 112, 4485, 10.1182/blood-2008-05-159848 · DOI
- Juntilla, 2010, AKT1 and AKT2 maintain hematopoietic stem cell function by regulating reactive oxygen species, Blood, 115, 4030, 10.1182/blood-2009-09-241000 · DOI · Paper page
- Kharas, 2010, Constitutively active AKT depletes hematopoietic stem cells and induces leukemia in mice, Blood, 115, 1406, 10.1182/blood-2009-06-229443 · DOI · Paper page
- Le Belle, 2011, Proliferative neural stem cells have high endogenous ROS levels that regulate self-renewal and neurogenesis in a PI3K/Akt-dependent manner, Cell Stem Cell, 8, 59, 10.1016/j.stem.2010.11.028 · DOI · Paper page
- Cho, 2004, Redox regulation of PTEN and protein tyrosine phosphatases in H2O2 mediated cell signaling, FEBS Lett, 560, 7, 10.1016/S0014-5793(04)00112-7 · DOI · Paper page
- Salmeen, 2005, Functions and mechanisms of redox regulation of cysteine-based phosphatases, Antioxid. Redox Signaling, 7, 560, 10.1089/ars.2005.7.560 · DOI · Paper page
- Yilmaz, 2006, Pten dependence distinguishes haematopoietic stem cells from leukaemia-initiating cells, Nature, 441, 475, 10.1038/nature04703 · DOI · Paper page
- Lee, 2010, mTOR activation induces tumor suppressors that inhibit leukemogenesis and deplete hematopoietic stem cells after Pten deletion, Cell Stem Cell, 7, 593, 10.1016/j.stem.2010.09.015 · DOI · Paper page
- Li, 2010, Physiological levels of reactive oxygen species are required to maintain genomic stability in stem cells, Stem Cells, 28, 1178, 10.1002/stem.438 · DOI · Paper page
- Rizo, 2009, Repression of BMI1 in normal and leukemic human CD34(+) cells impairs self-renewal and induces apoptosis, Blood, 114, 1498, 10.1182/blood-2009-03-209734 · DOI · Paper page
- Facchino, 2010, BMI1 confers radioresistance to normal and cancerous neural stem cells through recruitment of the DNA damage response machinery, J. Neurosci, 30, 10096, 10.1523/JNEUROSCI.1634-10.2010 · DOI · Paper page
- Chuikov, 2010, Prdm16 promotes stem cell maintenance in multiple tissues, partly by regulating oxidative stress, Nat. Cell Biol, 12, 999, 10.1038/ncb2101 · DOI · Paper page
- Maryanovich, 2012, The ATM–BID pathway regulates quiescence and survival of haematopoietic stem cells, Nat. Cell Biol, 14, 535, 10.1038/ncb2468 · DOI
- Abbas, 2010, Mdm2 is required for survival of hematopoietic stem cells/progenitors via dampening of ROS-induced p53 activity, Cell Stem Cell, 7, 606, 10.1016/j.stem.2010.09.013 · DOI
- Abbas, 2011, The ups and downs of p53 regulation in hematopoietic stem cells, Cell Cycle, 10, 3257, 10.4161/cc.10.19.17721 · DOI
- Wilson, 2006, Bone-marrow haematopoietic-stem-cell niches, Nat. Rev. Immunol., 6, 93, 10.1038/nri1779 · DOI · Paper page
- Yin, 2006, The stem cell niches in bone, J. Clin. Invest., 116, 1195, 10.1172/JCI28568 · DOI · Paper page
- Mansour, 2012, Osteoclasts promote the formation of hematopoietic stem cell niches in the bone marrow, J. Exp. Med, 209, 537, 10.1084/jem.20110994 · DOI · Paper page
- Mendez-Ferrer, 2010, Mesenchymal and haematopoietic stem cells form a unique bone marrow niche, Nature, 466, 829, 10.1038/nature09262 · DOI · Paper page
- Winkler, 2010, Bone marrow macrophages maintain hematopoietic stem cell (HSC) niches and their depletion mobilizes HSCs, Blood, 116, 4815, 10.1182/blood-2009-11-253534 · DOI · Paper page
- Chow, 2011, Bone marrow CD169+ macrophages promote the retention of hematopoietic stem and progenitor cells in the mesenchymal stem cell niche, J. Exp. Med, 208, 261, 10.1084/jem.20101688 · DOI · Paper page
- Fujisaki, 2011, In vivo imaging of Treg cells providing immune privilege to the haematopoietic stem-cell niche, Nature, 474, 216, 10.1038/nature10160 · DOI · Paper page
- Doan, 2012, The vascular niche: home for normal and malignant hematopoietic stem cells, Leukemia, 26, 54, 10.1038/leu.2011.236 · DOI
- Guerrouahen, 2011, Osteoblastic and vascular endothelial niches, their control on normal hematopoietic stem cells, and their consequences on the development of leukemia, Stem Cells Int., 2011, 375857, 10.4061/2011/375857 · DOI
- Hoggatt, 2011, Many mechanisms mediating mobilization: an alliterative review, Curr. Opin. Hematol., 18, 231, 10.1097/MOH.0b013e3283477962 · DOI
- Hoggatt, 2011, Mobilization of hematopoietic stem cells from the bone marrow niche to the blood compartment, Stem Cell Res. Ther, 2, 13, 10.1186/scrt54 · DOI
- Lam, 2010, Hematopoietic stem cell lodgment in the adult bone marrow stem cell niche, Int. J. Lab. Hematol, 32, 551, 10.1111/j.1751-553X.2010.01250.x · doi:10.1111/j.1751-553x.2010.01250.x
- Suarez-Alvarez, 2012, Mobilization and homing of hematopoietic stem cells, Adv. Exp. Med. Biol., 741, 152, 10.1007/978-1-4614-2098-9_11 · DOI
- Ren, 2010, ERK1/2-Akt1 crosstalk regulates arteriogenesis in mice and zebrafish, J. Clin. Invest, 120, 1217, 10.1172/JCI39837 · DOI
- Cipolleschi, 1993, The role of hypoxia in the maintenance of hematopoietic stem cells, Blood, 82, 2031, 10.1182/blood.V82.7.2031.2031 · DOI · Paper page
- Danet, 2003, Expansion of human SCID-repopulating cells under hypoxic conditions, J. Clin. Invest., 112, 126, 10.1172/JCI17669 · DOI · Paper page
- Ivanovic, 2000, Incubation of murine bone marrow cells in hypoxia ensures the maintenance of marrow-repopulating ability together with the expansion of committed progenitors, Br. J. Haematol, 108, 424, 10.1046/j.1365-2141.2000.01842.x · DOI
- Winkler, 2010, Positioning of bone marrow hematopoietic and stromal cells relative to blood flow in vivo: serially reconstituting hematopoietic stem cells reside in distinct nonperfused niches, Blood, 116, 375, 10.1182/blood-2009-07-233437 · DOI · Paper page
- Takubo, 2010, Regulation of the HIF-1alpha level is essential for hematopoietic stem cells, Cell Stem Cell, 7, 391, 10.1016/j.stem.2010.06.020 · DOI · Paper page
- Bromberg, 2012, Osteoblastic N-cadherin is not required for microenvironmental support and regulation of hematopoietic stem and progenitor cells, Blood, 120, 303, 10.1182/blood-2011-09-377853 · DOI
- Greenbaum, 2012, N-cadherin in osteolineage cells is not required for maintenance of hematopoietic stem cells, Blood, 120, 295, 10.1182/blood-2011-09-377457 · DOI
- Kiel, 2009, Hematopoietic stem cells do not depend on N-cadherin to regulate their maintenance, Cell Stem Cell, 4, 170, 10.1016/j.stem.2008.10.005 · DOI · Paper page
- Lewandowski, 2010, In vivo cellular imaging pinpoints the role of reactive oxygen species in the early steps of adult hematopoietic reconstitution, Blood, 115, 443, 10.1182/blood-2009-05-222711 · DOI
- Kobayashi, 2010, Angiocrine factors from Akt-activated endothelial cells balance self-renewal and differentiation of haematopoietic stem cells, Nat. Cell Biol, 12, 1046, 10.1038/ncb2108 · DOI · Paper page
- Taniguchi Ishikawa, 2012, Connexin-43 prevents hematopoietic stem cell senescence through transfer of reactive oxygen species to bone marrow stromal cells, Proc. Natl. Acad. Sci. USA, 109, 9071, 10.1073/pnas.1120358109 · DOI
- Aicher, 2005, Mobilizing endothelial progenitor cells, Hypertension, 45, 321, 10.1161/01.HYP.0000154789.28695.ea · DOI · Paper page
- Dimmeler, 2010, Regulation of bone marrow-derived vascular progenitor cell mobilization and maintenance, Arterioscler. Thromb. Vasc. Biol, 30, 1088, 10.1161/ATVBAHA.109.191668 · DOI
- Krankel, 2011, Targeting stem cell niches and trafficking for cardiovascular therapy, Pharmacol. Ther, 129, 62, 10.1016/j.pharmthera.2010.10.002 · DOI
- Levesque, 2007, Hematopoietic progenitor cell mobilization results in hypoxia with increased hypoxia-inducible transcription factor-1 alpha and vascular endothelial growth factor A in bone marrow, Stem Cells, 25, 1954, 10.1634/stemcells.2006-0688 · DOI
- van Os, 2000, Respiratory burst of neutrophils is not required for stem cell mobilization in mice, Br. J. Haematol, 111, 695, 10.1111/j.1365-2141.2000.02374.x · doi:10.1111/j.1365-2141.2000.02374.x
- Fan, 2007, Role of the plasma membrane ROS-generating NADPH oxidase in CD34+ progenitor cells preservation by hypoxia, J. Biotechnol, 130, 455, 10.1016/j.jbiotec.2007.05.023 · DOI
- Edlund, 2010, The roles of NADPH-oxidase and nNOS for the increased oxidative stress and the oxygen consumption in the diabetic kidney, Diabetes Metab. Res. Rev, 26, 349, 10.1002/dmrr.1099 · DOI
- Lee, 2010, Inhibition of respiration extends C. elegans life span via reactive oxygen species that increase HIF-1 activity, Curr. Biol, 20, 2131, 10.1016/j.cub.2010.10.057 · DOI · Paper page
- Jiang, 2008, Angiogenesis by transplantation of HIF-1 alpha modified EPCs into ischemic limbs, J. Cell. Biochem., 103, 321, 10.1002/jcb.21416 · DOI
- Rey, 2009, Synergistic effect of HIF-1alpha gene therapy and HIF-1-activated bone marrow-derived angiogenic cells in a mouse model of limb ischemia, Proc. Natl. Acad. Sci. USA, 106, 20399, 10.1073/pnas.0911921106 · DOI
- Kucia, 2004, Cells expressing early cardiac markers reside in the bone marrow and are mobilized into the peripheral blood after myocardial infarction, Circ. Res, 95, 1191, 10.1161/01.RES.0000150856.47324.5b · DOI · Paper page
- Schober, 2008, Chemokines in vascular dysfunction and remodeling, Arterioscler. Thromb. Vasc. Biol., 28, 1950, 10.1161/ATVBAHA.107.161224 · DOI · Paper page
- Pillarisetti, 2001, Cloning and relative expression analysis of rat stromal cell derived factor-1 (SDF-1)1: SDF-1 alpha mRNA is selectively induced in rat model of myocardial infarction, Inflammation, 25, 293, 10.1023/A:1012808525370 · DOI · Paper page
- Cramer, 2003, HIF-1alpha is essential for myeloid cell-mediated inflammation, Cell, 112, 645, 10.1016/S0092-8674(03)00154-5 · DOI · Paper page
- Ceradini, 2004, Progenitor cell trafficking is regulated by hypoxic gradients through HIF-1 induction of SDF-1, Nat. Med, 10, 858, 10.1038/nm1075 · DOI · Paper page
- Golan, 2012, S1P promotes murine progenitor cell egress and mobilization via S1P1-mediated ROS signaling and SDF-1 release, Blood, 119, 2478, 10.1182/blood-2011-06-358614 · DOI · Paper page
- Page-McCaw, 2007, Matrix metalloproteinases and the regulation of tissue remodelling, Nat. Rev. Mol. Cell Biol., 8, 221, 10.1038/nrm2125 · DOI · Paper page
- Masuda, 2011, Methodological development of a clonogenic assay to determine endothelial progenitor cell potential, Circ. Res, 109, 20, 10.1161/CIRCRESAHA.110.231837 · DOI
- Wang, 2010, Proteomic analysis of interstitial fluid in bone marrow identified that peroxiredoxin 2 regulates H2O2 level of bone marrow during aging, J. Proteome Res, 9, 3812, 10.1021/pr901180w · DOI
- Chen, 2004, Number and activity of endothelial progenitor cells from peripheral blood in patients with hypercholesterolaemia, Clin. Sci. (London), 107, 273, 10.1042/CS20030389 · DOI · Paper page
- Fadini, 2005, Circulating endothelial progenitor cells are reduced in peripheral vascular complications of type 2 diabetes mellitus, J. Am. Coll. Cardiol, 45, 1449, 10.1016/j.jacc.2004.11.067 · DOI · Paper page
- Fadini, 2008, Gender differences in endothelial progenitor cells and cardiovascular risk profile: the role of female estrogens, Arterioscler. Thromb. Vasc. Biol, 28, 997, 10.1161/ATVBAHA.107.159558 · DOI · Paper page
- Imanishi, 2005, Angiotensin II accelerates endothelial progenitor cell senescence through induction of oxidative stress, J. Hypertens, 23, 97, 10.1097/00004872-200501000-00018 · DOI · Paper page
- Loomans, 2004, Endothelial progenitor cell dysfunction: a novel concept in the pathogenesis of vascular complications of type 1 diabetes, Diabetes, 53, 195, 10.2337/diabetes.53.1.195 · DOI · Paper page
- Oliveras, 2008, Endothelial progenitor cells are reduced in refractory hypertension, J. Hum. Hypertens, 22, 183, 10.1038/sj.jhh.1002304 · DOI
- Urbich, 2005, Risk factors for coronary artery disease, circulating endothelial progenitor cells, and the role of HMG-CoA reductase inhibitors, Kidney Int, 67, 1672, 10.1111/j.1523-1755.2005.00261.x · DOI
- Valgimigli, 2004, CD34+ and endothelial progenitor cells in patients with various degrees of congestive heart failure, Circulation, 110, 1209, 10.1161/01.CIR.0000136813.89036.21 · DOI · Paper page
- Vasa, 2001, Number and migratory activity of circulating endothelial progenitor cells inversely correlate with risk factors for coronary artery disease, Circ. Res, 89, E1, 10.1161/hh1301.093953 · DOI · Paper page
- Fadini, 2010, Circulating progenitor cell count for cardiovascular risk stratification: a pooled analysis, PLoS One, 5, e11488, 10.1371/journal.pone.0011488 · DOI
- Thum, 2007, Endothelial nitric oxide synthase uncoupling impairs endothelial progenitor cell mobilization and function in diabetes, Diabetes, 56, 666, 10.2337/db06-0699 · DOI · Paper page
- Zhang, 2008, Biphasic response of endothelial progenitor cell proliferation induced by high glucose and its relationship with reactive oxygen species, J. Endocrinol, 197, 463, 10.1677/JOE-08-0036 · DOI
- Di Stefano, 2009, p66ShcA modulates oxidative stress and survival of endothelial progenitor cells in response to high glucose, Cardiovasc. Res, 82, 421, 10.1093/cvr/cvp082 · DOI
- Ceradini, 2008, Decreasing intracellular superoxide corrects defective ischemia-induced new vessel formation in diabetic mice, J. Biol. Chem, 283, 10930, 10.1074/jbc.M707451200 · DOI · Paper page
- Galasso, 2006, Impaired angiogenesis in glutathione peroxidase-1-deficient mice is associated with endothelial progenitor cell dysfunction, Circ. Res, 98, 254, 10.1161/01.RES.0000200740.57764.52 · DOI · Paper page
- Ingram, 2007, Clonogenic endothelial progenitor cells are sensitive to oxidative stress, Stem Cells, 25, 297, 10.1634/stemcells.2006-0340 · DOI
- Dai, 2011, Cleaved high-molecular-weight kininogen accelerates the onset of endothelial progenitor cell senescence by induction of reactive oxygen species, Arterioscler. Thromb. Vasc. Biol, 31, 883, 10.1161/ATVBAHA.110.222430 · DOI
- Tongers, 2011, Stem and progenitor cell-based therapy in ischaemic heart disease: promise, uncertainties, and challenges, Eur. Heart J., 32, 1197, 10.1093/eurheartj/ehr018 · DOI · Paper page
- Ohshima, 2009, Antioxidant therapy attenuates diabetes-related impairment of bone marrow stem cells, Circ. J., 73, 162, 10.1253/circj.CJ-08-0123 · DOI
- Callaghan, 2005, Hyperglycemia-induced reactive oxygen species and impaired endothelial progenitor cell function, Antioxid. Redox Signaling, 7, 1476, 10.1089/ars.2005.7.1476 · DOI
- Yao, 2007, Losartan improves the impaired function of endothelial progenitor cells in hypertension via an antioxidant effect, Hypertens. Res, 30, 1119, 10.1291/hypres.30.1119 · DOI
- Yao, 2008, Effects of the antioxidative beta-blocker celiprolol on endothelial progenitor cells in hypertensive rats, Am. J. Hypertens, 21, 1062, 10.1038/ajh.2008.233 · DOI
- Thum, 2007, Differential effects of organic nitrates on endothelial progenitor cells are determined by oxidative stress. Arterioscler, Thromb. Vasc. Biol, 27, 748, 10.1161/01.ATV.0000258787.18982.73 · DOI
- Thum, 2011, Organic nitrates differentially modulate circulating endothelial progenitor cells and endothelial function in patients with symptomatic coronary artery disease, Antioxid. Redox Signaling, 15, 925, 10.1089/ars.2010.3503 · doi:10.1089/ars.2010.3503
- Song, 2010, Reactive oxygen species inhibit adhesion of mesenchymal stem cells implanted into ischemic myocardium via interference of focal adhesion complex, Stem Cells, 28, 555, 10.1002/stem.302 · DOI · Paper page
- Kubo, 2008, Hypoxic preconditioning increases survival and angiogenic potency of peripheral blood mononuclear cells via oxidative stress resistance, Am. J. Physiol. Heart Circ. Physiol, 294, H590, 10.1152/ajpheart.00856.2007 · DOI
- Kubo, 2007, Short-term pretreatment with low-dose hydrogen peroxide enhances the efficacy of bone marrow cells for therapeutic angiogenesis, Am. J. Physiol. Heart Circ. Physiol, 292, H2582, 10.1152/ajpheart.00786.2006 · DOI
- Carriere, 2009, Preconditioning by mitochondrial reactive oxygen species improves the proangiogenic potential of adipose-derived cells-based therapy, Arterioscler. Thromb. Vasc. Biol, 29, 1093, 10.1161/ATVBAHA.109.188318 · DOI
- Tojo, 2005, Role of gp91phox (Nox2)-containing NAD(P)H oxidase in angiogenesis in response to hindlimb ischemia, Circulation, 111, 2347, 10.1161/01.CIR.0000164261.62586.14 · DOI · Paper page
- Haddad, 2011, Nox2-derived reactive oxygen species contribute to hypercholesterolemia-induced inhibition of neovascularization: effects on endothelial progenitor cells and mature endothelial cells, Atherosclerosis, 217, 340, 10.1016/j.atherosclerosis.2011.03.038 · DOI
- Haddad, 2009, Nox2-containing NADPH oxidase deficiency confers protection from hindlimb ischemia in conditions of increased oxidative stress, Arterioscler. Thromb. Vasc. Biol, 29, 1522, 10.1161/ATVBAHA.109.191437 · DOI
- Turgeon, 2012, Protection against vascular aging in Nox2-deficient mice: impact on endothelial progenitor cells and reparative neovascularization, Atherosclerosis, 223, 122, 10.1016/j.atherosclerosis.2012.05.003 · DOI
- Adams, 2006, Stem cell engraftment at the endosteal niche is specified by the calcium-sensing receptor, Nature, 439, 599, 10.1038/nature04247 · DOI · Paper page
- Walkley, 2007, A microenvironment-induced myeloproliferative syndrome caused by retinoic acid receptor gamma deficiency, Cell, 129, 1097, 10.1016/j.cell.2007.05.014 · DOI · Paper page
- Oikawa, 2010, Diabetes mellitus induces bone marrow microangiopathy, Arterioscler. Thromb. Vasc. Biol., 30, 498, 10.1161/ATVBAHA.109.200154 · DOI · Paper page
- Amrani, 2011, The Paf oncogene is essential for hematopoietic stem cell function and development, J. Exp. Med, 208, 1757, 10.1084/jem.20102170 · DOI
- Wang, 2011, AMP-activated protein kinase rescues the angiogenic functions of endothelial progenitor cells via manganese superoxide dismutase induction in type 1 diabetes, Am. J. Physiol. Endocrinol. Metab, 300, E1135, 10.1152/ajpendo.00001.2011 · DOI
- Hole, 2010, Ras-induced reactive oxygen species promote growth factor-independent proliferation in human CD34+ hematopoietic progenitor cells, Blood, 115, 1238, 10.1182/blood-2009-06-222869 · DOI
- Chen, 2010, Advanced glycation endproducts alter functions and promote apoptosis in endothelial progenitor cells through receptor for advanced glycation endproducts mediated overexpression of cell oxidant stress, Mol. Cell. Biochem, 335, 137, 10.1007/s11010-009-0250-y · DOI
- Wang, 2009, Hemin promotes proliferation and differentiation of endothelial progenitor cells via activation of AKT and ERK, J. Cell Physiol, 219, 617, 10.1002/jcp.21711 · DOI
- Schraml, 2009, Acute adrenergic stress inhibits proliferation of murine hematopoietic progenitor cells via p38/MAPK signaling, Stem Cells Dev, 18, 215, 10.1089/scd.2008.0072 · DOI
- You, 2008, Hypertension impairs postnatal vasculogenesis: role of antihypertensive agents, Hypertension, 51, 1537, 10.1161/HYPERTENSIONAHA.107.109066 · DOI
- Prus, 2007, The effect of the copper chelator tetraethylenepentamine on reactive oxygen species generation by human hematopoietic progenitor cells, Stem Cells Dev, 16, 1053, 10.1089/scd.2007.0052 · DOI
- Zhang, 2007, Inflammatory ROS promote and cooperate with the Fanconi anemia mutation for hematopoietic senescence, J. Cell Sci, 120, 1572, 10.1242/jcs.003152 · DOI
- Iiyama, 2006, Reactive oxygen species generated by hematopoietic cytokines play roles in activation of receptor-mediated signaling and in cell cycle progression, Cell Signalling, 18, 174, 10.1016/j.cellsig.2005.04.002 · DOI
Cited by
Cellular mechanisms and physiological consequences of redox-dependent signalling
Holmström, K. M., & Finkel, T. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3801 · Cited by 2,093
Stem cells and the impact of ROS signaling
Bigarella, C. L., Liang, R., & Ghaffari, S. (2014) · Development · doi:10.1242/dev.107086 · Cited by 632
Chaperone-mediated autophagy sustains haematopoietic stem-cell function
Dong, S., Wang, Q., Kao, Y.-R., Diaz, A., Tasset, I., Kaushik, S., Thiruthuvanathan, V., Zintiridou, A., Nieves, E., Dzieciatkowska, M., et al. (2021) · Nature · doi:10.1038/s41586-020-03129-z · Cited by 275
Oxidative Stress, Bone Marrow Failure, and Genome Instability in Hematopoietic Stem Cells
Richardson, C., Yan, S., & Vestal, C. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms16022366 · Cited by 81
Wlaschek, M., Singh, K., Sindrilaru, A., Crisan, D., & Scharffetter-Kochanek, K. (2019) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2018.09.036 · Cited by 76
“Nevertheless, there is compelling evidence that redox homeostasis and ROS at least regulate stem cell behavior of hematopoietic stem cells and their bone marrow niche [132].”
Background
Metadata
- Authors
- Urao, N., & Ushio-Fukai, M.
- Venue
- Free Radical Biology and Medicine
- Publisher
- Elsevier BV
- Published
- 2013-01
- Volume
- 54
- Pages
- 26-39
- ISSN
- 0891-5849 (ISSN-L)
- OpenAlex
- W2020712259
- Cited by
- 168
- References
- 17
- FWCI
- 10.37
- Type
- journal article
- Language
- en
- Open access
- green
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Funders
- National Institutes of Health (077524, HL077524-S1)
- American Heart Association (0970336N, 09POST2250151, 12SDG12060100)
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Redox regulation of stem/progenitor cells and bone marrow niche. https://app.cochat.ai/papers/10.1016/j.freeradbiomed.2012.10.532
- The paper
- Urao, N., & Ushio-Fukai, M. (2013). Redox regulation of stem/progenitor cells and bone marrow niche. Free Radical Biology and Medicine. https://doi.org/10.1016/j.freeradbiomed.2012.10.532
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.