Cited by 23

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Roles of angiopoietin-like proteins in regulation of stem cell activity

Kadomatsu, Tsuyoshi, Oike, Yuichi·2019·The Journal of Biochemistry

Abstract

Various types of stem cells reside in the body and self-renew throughout an organism’s lifetime. Such self-renewal is essential for maintenance of tissue homeostasis and is co-ordinately regulated by stem cell-intrinsic signals and signals from stem cell niche. Angiopoietin is a niche-derived signalling molecule well known to contribute to maintenance of haematopoietic stem cells (HSCs). Angiopoietin-like proteins (ANGPTLs) are structurally similar to angiopoietin, and recent studies reveal that they function in angiogenesis, lipid and energy metabolism and regulation of inflammation. However, unlike angiopoietins, activities of ANGPTLs in stem cell maintenance have remained unclear. Recently, several studies have reported an association of ANGPTL signalling with stem cell maintenance. Here, we summarize those findings with a focus on HSCs, intestinal stem cells, neural stem cells and cancer stem cells and discuss mechanisms underlying ANGPTL-mediated stem cell maintenance.

Overview

Integrity signals

Registry

Crossref · 10.1093/jb/mvz005

Cites

2 of 2 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Verification

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Citations

Cites

Show all 2 references

Research works printed but not linked: 52

  1. Zon, 2008, Intrinsic and extrinsic control of haematopoietic stem-cell self-renewal, Nature, 453, 306, 10.1038/nature07038 · DOI
  2. Chen, 2013, Adhesion in the stem cell niche: biological roles and regulation, Development, 140, 255, 10.1242/dev.083139 · DOI
  3. Yu, 2013, Structural basis for angiopoietin-1-mediated signaling initiation, Proc. Natl. Acad. Sci. USA, 110, 7205, 10.1073/pnas.1216890110 · DOI
  4. Mendelson, 2014, Hematopoietic stem cell niche maintenance during homeostasis and regeneration, Nat. Med., 20, 833, 10.1038/nm.3647 · DOI
  5. Kim, 1999, Molecular cloning, expression, and characterization of angiopoietin-related protein. Angiopoietin-related protein induces endothelial cell sprouting, J. Biol. Chem., 274, 26523, 10.1074/jbc.274.37.26523 · DOI
  6. Kadomatsu, 2014, Diverse roles of ANGPTL2 in physiology and pathophysiology, Trends Endocrinol. Metab., 25, 245, 10.1016/j.tem.2014.03.012 · DOI
  7. Oike, 2003, Angiopoietin-related growth factor (AGF) promotes epidermal proliferation, remodeling, and regeneration, Proc. Natl. Acad. Sci. USA, 100, 9494, 10.1073/pnas.1531901100 · DOI
  8. Oike, 2004, Angiopoietin-related growth factor (AGF) promotes angiogenesis, Blood, 103, 3760, 10.1182/blood-2003-04-1272 · DOI
  9. Oike, 2005, Angiopoietin-related growth factor antagonizes obesity and insulin resistance, Nat. Med., 11, 400, 10.1038/nm1214 · DOI · Paper page
  10. Quagliarini, 2012, Atypical angiopoietin-like protein that regulates ANGPTL3, Proc. Natl. Acad. Sci. USA, 109, 19751, 10.1073/pnas.1217552109 · DOI · Paper page
  11. Arai, 2004, Tie2/angiopoietin-1 signaling regulates hematopoietic stem cell quiescence in the bone marrow niche, Cell, 118, 149, 10.1016/j.cell.2004.07.004 · DOI
  12. Takakura, 1998, Critical role of the TIE2 endothelial cell receptor in the development of definitive hematopoiesis, Immunity, 9, 677, 10.1016/S1074-7613(00)80665-2 · DOI
  13. Zhang, 2006, Angiopoietin-like proteins stimulate ex vivo expansion of hematopoietic stem cells, Nat. Med., 12, 240, 10.1038/nm1342 · DOI
  14. Blank, 2012, Angptl4 maintains in vivo repopulation capacity of CD34+ human cord blood cells, Eur. J. Haematol., 89, 198, 10.1111/j.1600-0609.2012.01812.x · DOI
  15. Zhang, 2008, Angiopoietin-like 5 and IGFBP2 stimulate ex vivo expansion of human cord blood hematopoietic stem cells as assayed by NOD/SCID transplantation, Blood, 111, 3415, 10.1182/blood-2007-11-122119 · DOI
  16. Xiao, 2015, ANGPTL7 regulates the expansion and repopulation of human hematopoietic stem and progenitor cells, Haematologica, 100, 585, 10.3324/haematol.2014.118612 · DOI
  17. Akhter, 2013, Dynamic roles of angiopoietin-like proteins 1, 2, 3, 4, 6 and 7 in the survival and enhancement of ex vivo expansion of bone-marrow hematopoietic stem cells, Protein Cell., 4, 220, 10.1007/s13238-013-2066-5 · DOI
  18. Fan, 2014, Low-dose insulin-like growth factor binding proteins 1 and 2 and angiopoietin-like protein 3 co-ordinately stimulate ex vivo expansion of human umbilical cord blood hematopoietic stem cells as assayed in NOD/SCID gamma null mice, Stem Cell Res. Ther., 5, 71, 10.1186/scrt460 · DOI
  19. Zheng, 2012, Inhibitory receptors bind ANGPTLs and support blood stem cells and leukaemia development, Nature, 485, 656, 10.1038/nature11095 · DOI
  20. Kitsos, 2005, Calmodulin-dependent protein kinase IV regulates hematopoietic stem cell maintenance, J. Biol. Chem., 280, 33101, 10.1074/jbc.M505208200 · DOI
  21. Chan, 2006, Shp-2 heterozygous hematopoietic stem cells have deficient repopulating ability due to diminished self-renewal, Exp. Hematol, 34, 1230, 10.1016/j.exphem.2006.04.017 · DOI
  22. Lin, 2015, Angiopoietin-like proteins stimulate HSPC development through interaction with notch receptor signaling, Elife, 4, e05544, 10.7554/eLife.05544 · DOI
  23. Zheng, 2011, Angiopoietin-like protein 3 supports the activity of hematopoietic stem cells in the bone marrow niche, Blood, 117, 470, 10.1182/blood-2010-06-291716 · DOI
  24. Ng, 2007, Ikaros and chromatin regulation in early hematopoiesis, Curr. Opin. Immunol., 19, 116, 10.1016/j.coi.2007.02.014 · DOI
  25. Chou, 2010, Fetal liver hepatic progenitors are supportive stromal cells for hematopoietic stem cells, Proc. Natl. Acad. Sci. USA, 107, 7799, 10.1073/pnas.1003586107 · DOI
  26. Xiao, 2015, Loss of Angiopoietin-like 7 diminishes the regeneration capacity of hematopoietic stem and progenitor cells, J. Hematol. Oncol, 8, 7, 10.1186/s13045-014-0102-4 · DOI
  27. Smith-Berdan, 2011, Robo4 cooperates with CXCR4 to specify hematopoietic stem cell localization to bone marrow niches, Cell Stem Cell, 8, 72, 10.1016/j.stem.2010.11.030 · DOI
  28. Jackson, 2012, HOXB4 can enhance the differentiation of embryonic stem cells by modulating the hematopoietic niche, Stem Cells, 30, 150, 10.1002/stem.782 · DOI
  29. Reya, 2003, A role for Wnt signalling in self-renewal of haematopoietic stem cells, Nature, 423, 409, 10.1038/nature01593 · DOI · Paper page
  30. Gu, 2016, Sorting protein VPS33B regulates exosomal autocrine signaling to mediate hematopoiesis and leukemogenesis, J. Clin. Invest, 126, 4537, 10.1172/JCI87105 · DOI
  31. Tabata, 2009, Angiopoietin-like protein 2 promotes chronic adipose tissue inflammation and obesity-related systemic insulin resistance, Cell Metab, 10, 178, 10.1016/j.cmet.2009.08.003 · DOI
  32. Odagiri, 2014, The secreted protein ANGPTL2 promotes metastasis of osteosarcoma cells through integrin a5b1, p38 MAPK, and matrix metalloproteinases, Sci. Signal, 7, ra7, 10.1126/scisignal.2004612 · DOI
  33. Horiguchi, 2017, ANGPTL2 expression in the intestinal stem cell niche controls epithelial regeneration and homeostasis, Embo. J., 36, 409, 10.15252/embj.201695690 · DOI
  34. Horiguchi, 2014, Angiopoietin-like protein 2 renders colorectal cancer cells resistant to chemotherapy by activating spleen tyrosine kinase-phosphoinositide 3-kinase-dependent anti-apoptotic signaling, Cancer Sci., 105, 1550, 10.1111/cas.12554 · DOI
  35. Camenisch, 2002, ANGPTL3 stimulates endothelial cell adhesion and migration via integrin avb3 and induces blood vessel formation in vivo, J. Biol. Chem, 277, 17281, 10.1074/jbc.M109768200 · DOI
  36. Goh, 2010, Angiopoietin-like 4 interacts with integrins b1 and b5 to modulate keratinocyte migration, Am. J. Pathol, 177, 2791, 10.2353/ajpath.2010.100129 · DOI
  37. van der Loo, 1998, VLA-5 is expressed by mouse and human long-term repopulating hematopoietic cells and mediates adhesion to extracellular matrix protein fibronectin, J. Clin. Invest., 102, 1051, 10.1172/JCI3687 · DOI
  38. Vermeulen, 2014, Stem cell dynamics in homeostasis and cancer of the intestine, Nat. Rev. Cancer, 14, 468, 10.1038/nrc3744 · DOI
  39. Milne, 2017, Mouse models of MLL leukemia: recapitulating the human disease, Blood, 129, 2217, 10.1182/blood-2016-10-691428 · DOI
  40. Kang, 2018, CAMKs support development of acute myeloid leukemia, J. Hematol. Oncol, 11, 30, 10.1186/s13045-018-0574-8 · DOI
  41. Aoi, 2011, Angiopoietin-like protein 2 is an important facilitator of inflammatory carcinogenesis and metastasis, Cancer Res, 71, 7502, 10.1158/0008-5472.CAN-11-1758 · DOI
  42. Endo, 2012, Tumor cell-derived angiopoietin-like protein ANGPTL2 is a critical driver of metastasis, Cancer Res, 72, 1784, 10.1158/0008-5472.CAN-11-3878 · DOI
  43. Batlle, 2017, Cancer stem cells revisited, Nat. Med., 23, 1124, 10.1038/nm.4409 · DOI · Paper page
  44. Androutsellis-Theotokis, 2010, Angiogenic factors stimulate growth of adult neural stem cells, PLoS One, 5, e9414, 10.1371/journal.pone.0009414 · DOI
  45. Androutsellis-Theotokis, 2006, Notch signalling regulates stem cell numbers in vitro and in vivo, Nature, 442, 823, 10.1038/nature04940 · DOI
  46. Ramasamy, 2014, NogoR1 and PirB signaling stimulates neural stem cell survival and proliferation, Stem Cells, 32, 1636, 10.1002/stem.1645 · DOI
  47. Temple, 2001, The development of neural stem cells, Nature, 414, 112, 10.1038/35102174 · DOI
  48. Oh, 2014, Stem cell aging: mechanisms, regulators and therapeutic opportunities, Nat. Med., 20, 870, 10.1038/nm.3651 · DOI · Paper page
  49. Tian, 2016, ANGPTL2 activity in cardiac pathologies accelerates heart failure by perturbing cardiac function and energy metabolism, Nat. Commun, 7, 13016, 10.1038/ncomms13016 · DOI
  50. Horio, 2014, Role of endothelial cell-derived angptl2 in vascular inflammation leading to endothelial dysfunction and atherosclerosis progression, Arterioscler. Thromb. Vasc. Biol., 34, 790, 10.1161/ATVBAHA.113.303116 · DOI
  51. Zhao, 2018, Age-dependent increase in angiopoietin-like protein 2 accelerates skeletal muscle loss in mice, J. Biol. Chem., 293, 1596, 10.1074/jbc.M117.814996 · DOI
  52. Shimatani, 2009, PD-1+ memory phenotype CD4+ T cells expressing C/EBPalpha underlie T cell immunodepression in senescence and leukemia, Proc. Natl. Acad. Sci. USA, 106, 15807, 10.1073/pnas.0908805106 · DOI

Cited by

Sorted by citations

See all 23

Metadata

Authors
Kadomatsu, T., & Oike, Y.
Affiliations
Department of Molecular Genetics, Graduate School of Medical Sciences, Kumamoto University, 1-1-1 Honjo, Chuo-ku, Kumamoto, Japan
Venue
The Journal of Biochemistry
Published
2019-01-23
Volume
165
Issue
4
Pages
309-315
ISSN
  • 0021-924X
  • 1756-2651
Cited by
23
References
2
Language
en
Funders
  • Ministry of Education, Culture, Sports, Science and Technology
  • MEXT (17H05652, 18K07236)
  • Core Research for Evolutional Science and Technology
  • CREST
  • Japan Science and Technology Agency (13417915)
  • CREST program of the Japan Agency (JP18gm0610007)

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: Roles of angiopoietin-like proteins in regulation of stem cell activity. https://app.cochat.ai/papers/10.1093/jb/mvz005
The paper
Kadomatsu, T., & Oike, Y. (2019). Roles of angiopoietin-like proteins in regulation of stem cell activity. The Journal of Biochemistry. https://doi.org/10.1093/jb/mvz005