Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Technical Report
  • Published:

In situ genetic analysis of cellular chimerism

Abstract

Copy number variants are a recently discovered source of large-scale genomic diversity present in all individuals. We capitalize on these inherent genomic differences, focusing on deletion polymorphisms, to develop informative fluorescence in situ hybridization probes with the ability to unequivocally distinguish between donor and recipient cells in situ. These probes are accurate, specific, highly polymorphic and, notably, can be used to assign genetic identity in situ in a completely gender-independent fashion. We anticipate that these polymorphic deletion probes will be useful in further understanding the dynamics of cellular chimerism after transplantation, including the details of chronic organ rejection, post-transplant lymphoproliferative disorder and graft-versus-host disease, and in optimizing future tissue engineering and pluripotent stem cell therapies.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1: Assessment of variable copy number states with polymorphic deletion probes.
Figure 2: FISH with PDPs in clinical bone marrow chimerism specimens.
Figure 3: In situ FISH using PDPs for assessment of chimerism in organ transplantation.
Figure 4: Informative potential of polymorphic deletion probes under Hardy-Weinberg equilibrium.
Figure 5: Experimental assessment of the informative potential of identified PDPs in 50 random individuals.

Similar content being viewed by others

References

  1. Krause, D.S. et al. Multi-organ, multi-lineage engraftment by a single bone marrow–derived stem cell. Cell 105, 369–377 (2001).

    Article  CAS  Google Scholar 

  2. Tran, S.D. et al. Differentiation of human bone marrow–derived cells into buccal epithelial cells in vivo: a molecular analytical study. Lancet 361, 1084–1088 (2003).

    Article  Google Scholar 

  3. Korbling, M. et al. Hepatocytes and epithelial cells of donor origin in recipients of peripheral-blood stem cells. N. Engl. J. Med. 346, 738–746 (2002).

    Article  Google Scholar 

  4. Jiang, S. et al. Transplanted human bone marrow contributes to vascular endothelium. Proc. Natl. Acad. Sci. USA 101, 16891–16896 (2004).

    Article  CAS  Google Scholar 

  5. Minami, E., Laflamme, M.A., Saffitz, J.E. & Murry, C.E. Extracardiac progenitor cells repopulate most major cell types in the transplanted human heart. Circulation 112, 2951–2958 (2005).

    Article  Google Scholar 

  6. Grimm, P.C. et al. Neointimal and tubulointerstitial infiltration by recipient mesenchymal cells in chronic renal-allograft rejection. N. Engl. J. Med. 345, 93–97 (2001).

    Article  CAS  Google Scholar 

  7. Iafrate, A.J. et al. Detection of large-scale variation in the human genome. Nat. Genet. 36, 949–951 (2004).

    Article  CAS  Google Scholar 

  8. Sebat, J. et al. Large-scale copy number polymorphism in the human genome. Science 305, 525–528 (2004).

    Article  CAS  Google Scholar 

  9. Conrad, D.F., Andrews, T.D., Carter, N.P., Hurles, M.E. & Pritchard, J.K. A high-resolution survey of deletion polymorphism in the human genome. Nat. Genet. 38, 75–81 (2006).

    Article  CAS  Google Scholar 

  10. Hinds, D.A., Kloek, A.P., Jen, M., Chen, X. & Frazer, K.A. Common deletions and SNPs are in linkage disequilibrium in the human genome. Nat. Genet. 38, 82–85 (2006).

    Article  CAS  Google Scholar 

  11. McCarroll, S.A. et al. Common deletion polymorphisms in the human genome. Nat. Genet. 38, 86–92 (2006).

    Article  CAS  Google Scholar 

  12. Oliver, D.H., Thompson, R.E., Griffin, C.A. & Eshleman, J.R. Use of single nucleotide polymorphisms (SNP) and real-time polymerase chain reaction for bone marrow engraftment analysis. J. Mol. Diagn. 2, 202–208 (2000).

    Article  CAS  Google Scholar 

  13. Mullally, A. & Ritz, J. Beyond HLA: the significance of genomic variation for allogeneic hematopoietic stem cell transplantation. Blood 109, 1355–1362 (2007).

    Article  CAS  Google Scholar 

  14. Hochberg, E.P. et al. A novel rapid single nucleotide polymorphism (SNP)-based method for assessment of hematopoietic chimerism after allogeneic stem cell transplantation. Blood 101, 363–369 (2003).

    Article  CAS  Google Scholar 

  15. Weber, J.L. & May, P.E. Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction. Am. J. Hum. Genet. 44, 388–396 (1989).

    CAS  PubMed  PubMed Central  Google Scholar 

  16. Jeffreys, A.J. Genetic fingerprinting. Nat. Med. 11, 1035–1039 (2005).

    Article  CAS  Google Scholar 

  17. Litt, M. & Luty, J.A. A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene. Am. J. Hum. Genet. 44, 397–401 (1989).

    CAS  PubMed  PubMed Central  Google Scholar 

  18. Sermon, K., Van Steirteghem, A. & Liebaers, I. Preimplantation genetic diagnosis. Lancet 363, 1633–1641 (2004).

    Article  Google Scholar 

  19. Buckle, V.J. & Kearney, L. New methods in cytogenetics. Curr. Opin. Genet. Dev. 4, 374–382 (1994).

    Article  CAS  Google Scholar 

  20. Laflamme, M.A. & Murry, C.E. Regenerating the heart. Nat. Biotechnol. 23, 845–856 (2005).

    Article  CAS  Google Scholar 

  21. Rando, T.A. Stem cells, ageing and the quest for immortality. Nature 441, 1080–1086 (2006).

    Article  CAS  Google Scholar 

  22. Lindvall, O. & Kokaia, Z. Stem cells for the treatment of neurological disorders. Nature 441, 1094–1096 (2006).

    Article  CAS  Google Scholar 

  23. Koike, N. et al. Tissue engineering: creation of long-lasting blood vessels. Nature 428, 138–139 (2004).

    Article  CAS  Google Scholar 

  24. Braak, H. & Del Tredici, K. Assessing fetal nerve cell grafts in Parkinson's disease. Nat. Med. 14, 483–485 (2008).

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We thank M. Han, J. Miller-Batten and J. Reid for excellent technical assistance. We thank C. Lee (Brigham and Women's Hospital) and S. Kantarci (Beth Israel Deaconess Medical Center) for helpful discussions and reagents. We thank S. Ogino for helpful discussions. This work was supported in part by intramural funding from the Department of Pathology, Massachusetts General Hospital to A.J.I.

Author information

Authors and Affiliations

Authors

Contributions

D.W. and A.J.I. conceived of the project idea, designed and performed experiments, and wrote the manuscript. L.M.S. designed and performed experiments. Q.V., A.N., H.S. and G.K. performed FISH assays. J.R.S. contributed the autopsy cardiac transplant case and provided helpful discussions. All contributed to the editing of the manuscript.

Corresponding author

Correspondence to A John Iafrate.

Ethics declarations

Competing interests

A provisional application by D.W. and A.J.I. for a patent with the US Patent Office for the use of polymorphic deletion probes is pending and has not yet been licensed.

Supplementary information

Supplementary Text and Figures

Supplementary Methods, Supplementary Figs. 1–4 and Supplementary Table 1 (PDF 403 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Wu, D., Vu, Q., Nguyen, A. et al. In situ genetic analysis of cellular chimerism. Nat Med 15, 215–219 (2009). https://doi.org/10.1038/nm.1862

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nm.1862

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing