TY - JOUR
T1 - Advances in preclinical hematopoietic stem cell models and possible implications for improving therapeutic transplantation
AU - Fraint, Ellen
AU - Ulloa, Bianca A.
AU - Feliz Norberto, María
AU - Potts, Kathryn S.
AU - Bowman, Teresa V.
N1 - Funding Information:
B.A.U. was supported by the MSTP training grant T32GM007288‐45. M.F.N. was supported by the NIH Postbaccalaureate Research Education Program (PREP) at Albert Einstein College of Medicine (R25‐GM104547). K.S.P. was supported by American Australian Association Sir Rupert Murdoch Postdoctoral Fellowship and the Einstein Training Program in Stem Cell Research funded by the Empire State Stem Cell Fund through New York State Department of Health Contract C30292GG. T.V.B. was supported by American Cancer Society RSG‐129527‐DDC, the Evans MDS Foundation, DOD BM180109, and 1R56DK121738‐01.
Funding Information:
DOD, Grant/Award Numbers: 1R56DK121738‐01, BM180109; Evans MDS Foundation; American Cancer Society, Grant/Award Number: RSG‐129527‐DDC; NYSTEM Empire State Stem Cell Fund, Grant/Award Number: C30292GG; American Australian Association Sir Rupert Murdoch Postdoctoral Fellowship; NIH Postbaccalaureate Research Education Program (PREP) at Albert Einstein College of Medicine, Grant/Award Number: R25‐GM104547; MSTP, Grant/Award Number: T32GM007288‐45 Funding information
Funding Information:
B.A.U. was supported by the MSTP training grant T32GM007288-45. M.F.N. was supported by the NIH Postbaccalaureate Research Education Program (PREP) at Albert Einstein College of Medicine (R25-GM104547). K.S.P. was supported by American Australian Association Sir Rupert Murdoch Postdoctoral Fellowship and the Einstein Training Program in Stem Cell Research funded by the Empire State Stem Cell Fund through New York State Department of Health Contract C30292GG. T.V.B. was supported by American Cancer Society RSG-129527-DDC, the Evans MDS Foundation, DOD BM180109, and 1R56DK121738-01.
Publisher Copyright:
© 2020 The Authors. STEM CELLS TRANSLATIONAL MEDICINE published by Wiley Periodicals LLC on behalf of AlphaMed Press.
PY - 2021/3
Y1 - 2021/3
N2 - Hematopoietic stem cell transplantation (HSCT) is a treatment for many malignant, congenital, and acquired hematologic diseases. Some outstanding challenges in the HSCT field include the paucity of immunologically-matched donors, our inability to effectively expand hematopoeitic stem cells (HSCs) ex vivo, and the high infection risk during engraftment. Scientists are striving to develop protocols to generate, expand, and maintain HSCs ex vivo, however these are not yet ready for clinical application. Given these problems, advancing our understanding of HSC specification, regulation, and differentiation in preclinical models is essential to improve the therapeutic utility of HSCT. In this review, we link biomedical researchers and transplantation clinicians by discussing the potential therapeutic implications of recent fundamental HSC research in model organisms. We consider deficiencies in current HSCT practice, such as problems achieving adequate cell dose for successful and rapid engraftment, immense inflammatory cascade activation after myeloablation, and graft-vs-host disease. Furthermore, we discuss recent advances in the field of HSC biology and transplantation made in preclinical models of zebrafish, mouse, and nonhuman primates that could inform emerging practice for clinical application.
AB - Hematopoietic stem cell transplantation (HSCT) is a treatment for many malignant, congenital, and acquired hematologic diseases. Some outstanding challenges in the HSCT field include the paucity of immunologically-matched donors, our inability to effectively expand hematopoeitic stem cells (HSCs) ex vivo, and the high infection risk during engraftment. Scientists are striving to develop protocols to generate, expand, and maintain HSCs ex vivo, however these are not yet ready for clinical application. Given these problems, advancing our understanding of HSC specification, regulation, and differentiation in preclinical models is essential to improve the therapeutic utility of HSCT. In this review, we link biomedical researchers and transplantation clinicians by discussing the potential therapeutic implications of recent fundamental HSC research in model organisms. We consider deficiencies in current HSCT practice, such as problems achieving adequate cell dose for successful and rapid engraftment, immense inflammatory cascade activation after myeloablation, and graft-vs-host disease. Furthermore, we discuss recent advances in the field of HSC biology and transplantation made in preclinical models of zebrafish, mouse, and nonhuman primates that could inform emerging practice for clinical application.
KW - graft-vs-host disease
KW - hematopoietic stem cells
KW - lineage tracing
KW - preclinical models
KW - transplantation
UR - http://www.scopus.com/inward/record.url?scp=85092474698&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85092474698&partnerID=8YFLogxK
U2 - 10.1002/sctm.20-0294
DO - 10.1002/sctm.20-0294
M3 - Review article
C2 - 33058566
AN - SCOPUS:85092474698
SN - 2157-6564
VL - 10
SP - 337
EP - 345
JO - Stem cells translational medicine
JF - Stem cells translational medicine
IS - 3
ER -