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Angiopoietin-like proteins stimulate ex vivo expansion of hematopoietic stem cells

Abstract

Successful ex vivo expansion of hematopoietic stem cells (HSCs) would greatly benefit the treatment of disease and the understanding of crucial questions of stem cell biology. Here we show, using microarray studies, that the HSC-supportive mouse fetal liver CD3+ cells specifically express the proteins angiopoietin-like 2 (Angptl2) and angiopoietin-like 3 (Angptl3). We observed a 24- or 30-fold net expansion of long-term HSCs by reconstitution analysis when we cultured highly enriched HSCs for 10 days in the presence of Angptl2 or Angptl3 together with saturating levels of other growth factors. The coiled-coil domain of Angptl2 was capable of stimulating expansion of HSCs. Furthermore, angiopoietin-like 5, angiopoietin-like 7 and microfibril-associated glycoprotein 4 also supported expansion of HSCs in culture.

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Figure 1: Angptl2 substantially stimulates ex vivo expansion of HSCs.
Figure 2: Immunoaffinity purification of Angptl2 from conditioned medium of transfected 293T cells.
Figure 3: Purified Angptl2 or Angptl3 stimulates ex vivo expansion of HSCs, measured by a limiting dilution assay.
Figure 4: Mammalian cell-specific post-translational modifications and the coiled-coil domain of Angptl2 are important for stimulation of ex vivo expansion of HSCs.
Figure 5: Purified mouse Angptl3, human Angptl5, human Angptl7 or human Mfap4 stimulated ex vivo expansion of HSCs.

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References

  1. Shizuru, J.A., Negrin, R.S. & Weissman, I.L. Hematopoietic stem and progenitor cells: clinical and preclinical regeneration of the hematolymphoid system. Annu. Rev. Med. 56, 509–538 (2005).

    Article  CAS  Google Scholar 

  2. Verma, I.M. & Weitzman, M.D. Gene therapy: twenty-first century medicine. Annu. Rev. Biochem 74, 711–738 (2005).

    Article  CAS  Google Scholar 

  3. Sauvageau, G., Iscove, N.N. & Humphries, R.K. In vitro and in vivo expansion of hematopoietic stem cells. Oncogene 23, 7223–7232 (2004).

    Article  CAS  Google Scholar 

  4. Sorrentino, B.P. Clinical strategies for expansion of haematopoietic stem cells. Nat. Rev. Immunol. 4, 878–888 (2004).

    Article  CAS  Google Scholar 

  5. Krosl, J. et al. In vitro expansion of hematopoietic stem cells by recombinant TAT-HOXB4 protein. Nat. Med. 9, 1428–1432 (2003).

    Article  CAS  Google Scholar 

  6. Willert, K. et al. Wnt proteins are lipid-modified and can act as stem cell growth factors. Nature 423, 448–452 (2003).

    Article  CAS  Google Scholar 

  7. Moore, K.A., Ema, H. & Lemischka, I.R. In vitro maintenance of highly purified, transplantable hematopoietic stem cells. Blood 89, 4337–4347 (1997).

    CAS  PubMed  Google Scholar 

  8. Fraser, C.C., Eaves, C.J., Szilvassy, S.J. & Humphries, R.K. Expansion in vitro of retrovirally marked totipotent hematopoietic stem cells. Blood 76, 1071–1076 (1990).

    CAS  PubMed  Google Scholar 

  9. Miller, C.L. & Eaves, C.J. Expansion in vitro of adult murine hematopoietic stem cells with transplantable lympho-myeloid reconstituting ability. Proc. Natl. Acad. Sci. USA 94, 13648–13653 (1997).

    Article  CAS  Google Scholar 

  10. Varnum-Finney, B. et al. Pluripotent, cytokine-dependent, hematopoietic stem cells are immortalized by constitutive Notch1 signaling. Nat. Med. 6, 1278–1281 (2000).

    Article  CAS  Google Scholar 

  11. Antonchuk, J., Sauvageau, G. & Humphries, R.K. HOXB4-induced expansion of adult hematopoietic stem cells ex vivo. Cell 109, 39–45 (2002).

    Article  CAS  Google Scholar 

  12. Reya, T. et al. A role for Wnt signalling in self-renewal of haematopoietic stem cells. Nature 423, 409–414 (2003).

    Article  CAS  Google Scholar 

  13. Zhang, C.C. & Lodish, H.F. Insulin-like growth factor 2 expressed in a novel fetal liver cell population is a growth factor for hematopoietic stem cells. Blood 103, 2513–2521 (2004).

    Article  CAS  Google Scholar 

  14. Zhang, C.C. & Lodish, H.F. Murine hematopoietic stem cells change their surface phenotype during ex vivo expansion. Blood 105, 4314–4320 (2005).

    Article  CAS  Google Scholar 

  15. Kim, I. et al. Molecular cloning, expression, and characterization of angiopoietin-related protein. angiopoietin-related protein induces endothelial cell sprouting. J. Biol. Chem. 274, 26523–26528 (1999).

    Article  CAS  Google Scholar 

  16. Conklin, D. et al. Identification of a mammalian angiopoietin-related protein expressed specifically in liver. Genomics 62, 477–482 (1999).

    Article  CAS  Google Scholar 

  17. Camargo, F.D., Green, R., Capetanaki, Y., Jackson, K.A. & Goodell, M.A. Single hematopoietic stem cells generate skeletal muscle through myeloid intermediates. Nat. Med. 9, 1520–1527 (2003).

    Article  CAS  Google Scholar 

  18. Oike, Y., Yasunaga, K. & Suda, T. Angiopoietin-related/angiopoietin-like proteins regulate angiogenesis. Int. J. Hematol. 80, 21–28 (2004).

    Article  CAS  Google Scholar 

  19. Yoon, J.C. et al. Peroxisome proliferator-activated receptor gamma target gene encoding a novel angiopoietin-related protein associated with adipose differentiation. Mol. Cell. Biol. 20, 5343–5349 (2000).

    Article  CAS  Google Scholar 

  20. Zeng, L. et al. Identification of a novel human angiopoietin-like gene expressed mainly in heart. J. Hum. Genet. 48, 159–162 (2003).

    Article  CAS  Google Scholar 

  21. Peek, R., van Gelderen, B.E., Bruinenberg, M. & Kijlstra, A. Molecular cloning of a new angiopoietinlike factor from the human cornea. Invest. Ophthalmol. Vis. Sci. 39, 1782–1788 (1998).

    CAS  PubMed  Google Scholar 

  22. Zhao, Z. et al. The gene for a human microfibril-associated glycoprotein is commonly deleted in Smith-Magenis syndrome patients. Hum. Mol. Genet. 4, 589–597 (1995).

    Article  CAS  Google Scholar 

  23. Yamamoto, T. et al. Molecular cloning and initial characterization of a novel fibrinogen-related gene, HFREP-1. Biochem. Biophys. Res. Commun. 193, 681–687 (1993).

    Article  CAS  Google Scholar 

  24. Arai, F. et al. Tie2/Angiopoietin-1 signaling regulates hematopoietic stem cell quiescence in the bone marrow niche. Cell 118, 149–161 (2004).

    Article  CAS  Google Scholar 

  25. Oike, Y. et al. Angiopoietin-related growth factor antagonizes obesity and insulin resistance. Nat. Med. 11, 400–408 (2005).

    Article  CAS  Google Scholar 

  26. Li, C.L. & Johnson, G.R. Stem cell factor enhances the survival but not the self-renewal of murine hematopoietic long-term repopulating cells. Blood 84, 408–414 (1994).

    CAS  PubMed  Google Scholar 

  27. de Haan, G. et al. In vitro generation of long-term repopulating hematopoietic stem cells by fibroblast growth factor-1. Dev. Cell 4, 241–251 (2003).

    Article  CAS  Google Scholar 

  28. Sitnicka, E. et al. The effect of thrombopoietin on the proliferation and differentiation of murine hematopoietic stem cells. Blood 87, 4998–5005 (1996).

    CAS  PubMed  Google Scholar 

  29. Nielsen, H., Engelbrecht, J., Brunak, S. & von Heijne, G. Identification of prokaryotic and eukaryotic signal peptides and prediction of their cleavage sites. Protein Eng. 10, 1–6 (1997).

    Article  CAS  Google Scholar 

  30. Bendtsen, J.D., Nielsen, H., von Heijne, G. & Brunak, S. Improved prediction of signal peptides: SignalP 3.0. J. Mol. Biol. 340, 783–795 (2004).

    Article  Google Scholar 

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Acknowledgements

We thank R&D Systems Inc. for providing purified bacterially expressed Angptl2, insect-expressed Angptl3 and bacterially expressed Angptl7, as well as monoclonal antibodies against human Angptl2. We are grateful to B. Zhou for help in protein expression, G. Paradis and M. Jennings in Massachusetts Institute of Technology flow cytometry core facility for cell sorting, and A. Babic for critically reading the manuscript. C.C.Z. is a Leukemia and Lymphoma Society Fellow. H.F.L. was supported by US National Institutes of Health grant R01 DK 067356 and from the Engineering Research Centers Program of the National Science Foundation under National Science Foundation Award Number EEC 9843342 through the Biotechnology Process Engineering Center at the Massachusetts Institute of Technology.

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Correspondence to Harvey F Lodish.

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Supplementary information

Supplementary Fig. 1

Analysis of Angptl2 mRNA expression in hematopoietic cells from mouse day 15 fetal liver or adult bone marrow cells by real-time PCR. (PDF 80 kb)

Supplementary Fig. 2

The majority of freshly isolated BM HSCs and all cultured BM HSCs bind to Angptl2. (PDF 51 kb)

Supplementary Table 1

List of transcripts encoding secreted and membrane proteins that are abundant in fetal liver CD3+ cells and low in adult splenic CD3+ cells and fetal liver Gr-1+ cells, identified from Affymetrix U74Bv2 and U74Cv2 mouse chips. (PDF 29 kb)

Supplementary Methods (PDF 0 kb)

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Zhang, C., Kaba, M., Ge, G. et al. Angiopoietin-like proteins stimulate ex vivo expansion of hematopoietic stem cells. Nat Med 12, 240–245 (2006). https://doi.org/10.1038/nm1342

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