Helen M. Blau


Data di nascita 8/5/1948
Luogo Londra (Inghilterra)
Nomina 10/10/2017
Disciplina Biologia delle cellule staminali e Medicina rigenerativa
Titolo Donald E. and Delia B. Baxter Foundation Professor for Stem Cell Biology

Principali premi, riconoscimenti e accademie
Elected Fellow, American Association for the Advancement of Science (AAAS) (1991), Senior Career Recognition Award of WICB, American Society of Cell Biology (1992), President, Society for Developmental Biology (1994-1995), Elected to National Academy of Medicine (formally Institute of Medicine) (1995), Elected to American Academy of Arts and Sciences (1996), FASEB Excellence in Science Award (1999), Donald E. and Delia B. Baxter Endowed Professorship (1999), McKnight Technological Innovations for Neuroscience Award (2001), Honorary Doctorate, University of Nijmegen, Holland (2003), Rolf-Sammet Fonds Visiting Professorship, University of Frankfurt (2003), Elected, Harvard Board of Overseers (2004-2010), President, International Society for Differentiation (2002-2004), Fulbright Senior Specialist Award (lnstitut Pasteur) (2007), AACR-Irving Weinstein Foundation Distinguished Lectureship and Award for Outstanding Innovations in Science (2011), NIH Director's Transformative Research Award (2011-2017), Stanford Office of Technology Licensing Outstanding Inventor Award and Hall of Fame (2015), Glenn Award for Research in Biological Mechanisms of Aging (2015), Elected to the National Academy of Sciences (2016), Elected to Pontifical Academy of Sciences (2017), Li Ka Shing Research Award (2017).

Riassunto dell'attività scientifica
Research in Dr. Blau's laboratory is focused on understanding principles of regenerative medicine. Her laboratory established that the differentiated state of specialized tissue-specific cells is not fixed and irreversible, but can be changed. This demonstration of cellular plasticity constituted a paradigm shift in our understanding of mammalian cell differentiation. Using muscle as a model, Blau's work provided the first definitive evidence that diverse cell types could be reprogrammed using non-dividing cell fusions. Her studies demonstrated that cell differentiation requires continuous regulation and that a shift in the stoichiometry of trans-acting regulators induces nuclear reprogramming. This body of work provided the scientific underpinnings for the induction of pluripotent stem cells. Blau applied this discovery to adult stem cell biology. She led the field with novel approaches to the isolation of muscle stem cells, maintenance of stem cell function on bioengineered platforms, and strategies for rejuvenating aged stem cell function. Her work provides the foundation for innovative stem cell based strategies to treat skeletal and cardiac disorders due to injury, disease or aging. Blau's research is at the crux of stem cell biology and regenerative medicine.

Pubblicazioni principali
Blau, H.M., Chiu, C.-P. and Webster, C. (1983) Cytoplasmic activation of human nuclear genes in stable heterokaryons. Cell 32:1171-1180; Blau, H.M., Pavlath, G.K., Hardeman, E.C., Chiu, C.-P., Si lberstein, L., Webster, S.G., Miller, S.C. and Webster, C. (1985) Plasticity of the differentiated state. Science 230:758-766; Dhawan, J., Pan, L.C., Pavlath, G.K., Travis, M.A., Lanctot, A.M. and Blau, H.M. (1991) Systemic delivery of human growth hormone by injection of genetically engineered myoblasts. Science 254:1509-1512; Gussoni, E., Pavlath, G.K., Lanctot, A.M., Sharma, K., Miller, R.G., Steinman, L. and Blau, H.M. (1992) Normal dystrophin transcripts detected in DMD patients after myoblast transplantation. Nature 356:435-438; Rastinejad, F. and Blau, H.M. (1993) Genetic complementation reveals novel regulatory role for 3' untranslated regions in growth and differentiation. Cell 72:903-917; Sacco, A., Doyonnas, R., Kraft, P., Vitorovic, S. and Blau H.M. (2008) Self-renewal and expansion of single transplanted muscle stem cells. Nature 456:502-506; Bhutani, N., Brady, J.J., Damian, M., Sacco, A., Corbel, S.Y. and Blau, H.M. (2010) Reprogramming towards pluripotency requires AID-dependent DNA demethylation. Nature 463(7284):1042-1047; Gilbert, P.M., Havenstrite, K.L., Magnusson, K.E.G., Sacco, A., Leonardi, N.A., Kraft, P., Nguyen, N.K., Thrun, S., Lutolf, M.P. and Blau, H.M. (2010) Substrate elasticity regulates skeletal muscle stem cell self-renewal in culture. Science 329(5995):1078-1081; Sacco, A., Mourkioti, F., Tran, R., Choi, J., Llewellyn, M., Kraft, P., Shkreli, M., Delp, S., Pomerantz, J.H., Artandi, S.E. and Blau, H.M. (2010) Short telomeres and stem cell exhaustion model Duchenne muscular dystrophy in mdx/mTR mice. Cell 143(7):1059-71; Cosgrove, B.D., Gilbert, P.M., Porpiglia, E., Mourkioti, F., Lee, S.P., Corbel, S.Y., Llewellyn, M.E., Delp, S.L. and Blau, H.M. (2014) Rejuvenation of the aged muscle stem cell population restores strength to injured aged muscles. Nature Medicine 20(3):255-264.

Indirizzo professionale

Stanford University School of Medicine
Microbiology and Immunology Department
269 Campus Drive
CCSR building room 4215
Stanford, California
94305 USA