Cargando…

Small-Molecule Ice Recrystallization Inhibitors Improve the Post-Thaw Function of Hematopoietic Stem and Progenitor Cells

[Image: see text] The success of hematopoietic stem cell transplantation depends in part on the number and the quality of cells transplanted. Cryoinjuries during freezing and thawing reduce the ability of hematopoietic stem and progenitor cells (HSPCs) to proliferate and differentiate after thawing....

Descripción completa

Detalles Bibliográficos
Autores principales: Briard, Jennie G., Jahan, Suria, Chandran, Priya, Allan, David, Pineault, Nicolas, Ben, Robert N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2016
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044699/
https://www.ncbi.nlm.nih.gov/pubmed/30023498
http://dx.doi.org/10.1021/acsomega.6b00178
_version_ 1783339524307288064
author Briard, Jennie G.
Jahan, Suria
Chandran, Priya
Allan, David
Pineault, Nicolas
Ben, Robert N.
author_facet Briard, Jennie G.
Jahan, Suria
Chandran, Priya
Allan, David
Pineault, Nicolas
Ben, Robert N.
author_sort Briard, Jennie G.
collection PubMed
description [Image: see text] The success of hematopoietic stem cell transplantation depends in part on the number and the quality of cells transplanted. Cryoinjuries during freezing and thawing reduce the ability of hematopoietic stem and progenitor cells (HSPCs) to proliferate and differentiate after thawing. Up to 20% of the patients undergoing umbilical cord blood (UCB) transplant experience delayed or failed engraftment, likely because of the inadequate hematopoietic potency of the unit. Therefore, the optimization of cryopreservation protocols, with an emphasis on the preservation of HSPCs, is an important issue. Current protocols typically utilize a 10% dimethyl sulfoxide cryoprotectant solution. This solution ensures 70–80% post-thaw cell viability by diluting intracellular solutes and maintaining the cell volume during cryopreservation. However, this solution fails to fully protect HSPCs, resulting in the loss of potency. Therefore, a new class of cryoprotectants (N-aryl-d-aldonamides) was designed and assessed for the ability to inhibit ice recrystallization and to protect HSPCs against cryoinjury. Several highly active ice recrystallization inhibitors were discovered. When used as additives to the conventional cryoprotectant solution, these nontoxic small molecules improved the preservation of functionally divergent hematopoietic progenitors in the colony-forming unit and long-term culture-initiating cell assays. By contrast, structurally similar compounds that did not inhibit ice recrystallization failed to improve the post-thaw recovery of myeloid progenitors. Together, these results demonstrate that the supplementation of cryopreservation solution with compounds capable of controlling ice recrystallization increases the post-thaw function and potency of HSPCs in UCB. This increase may translate into reduced risk of engraftment failure and allow for greater use of cryopreserved cord blood units.
format Online
Article
Text
id pubmed-6044699
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher American Chemical Society
record_format MEDLINE/PubMed
spelling pubmed-60446992018-07-16 Small-Molecule Ice Recrystallization Inhibitors Improve the Post-Thaw Function of Hematopoietic Stem and Progenitor Cells Briard, Jennie G. Jahan, Suria Chandran, Priya Allan, David Pineault, Nicolas Ben, Robert N. ACS Omega [Image: see text] The success of hematopoietic stem cell transplantation depends in part on the number and the quality of cells transplanted. Cryoinjuries during freezing and thawing reduce the ability of hematopoietic stem and progenitor cells (HSPCs) to proliferate and differentiate after thawing. Up to 20% of the patients undergoing umbilical cord blood (UCB) transplant experience delayed or failed engraftment, likely because of the inadequate hematopoietic potency of the unit. Therefore, the optimization of cryopreservation protocols, with an emphasis on the preservation of HSPCs, is an important issue. Current protocols typically utilize a 10% dimethyl sulfoxide cryoprotectant solution. This solution ensures 70–80% post-thaw cell viability by diluting intracellular solutes and maintaining the cell volume during cryopreservation. However, this solution fails to fully protect HSPCs, resulting in the loss of potency. Therefore, a new class of cryoprotectants (N-aryl-d-aldonamides) was designed and assessed for the ability to inhibit ice recrystallization and to protect HSPCs against cryoinjury. Several highly active ice recrystallization inhibitors were discovered. When used as additives to the conventional cryoprotectant solution, these nontoxic small molecules improved the preservation of functionally divergent hematopoietic progenitors in the colony-forming unit and long-term culture-initiating cell assays. By contrast, structurally similar compounds that did not inhibit ice recrystallization failed to improve the post-thaw recovery of myeloid progenitors. Together, these results demonstrate that the supplementation of cryopreservation solution with compounds capable of controlling ice recrystallization increases the post-thaw function and potency of HSPCs in UCB. This increase may translate into reduced risk of engraftment failure and allow for greater use of cryopreserved cord blood units. American Chemical Society 2016-11-28 /pmc/articles/PMC6044699/ /pubmed/30023498 http://dx.doi.org/10.1021/acsomega.6b00178 Text en Copyright © 2016 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Briard, Jennie G.
Jahan, Suria
Chandran, Priya
Allan, David
Pineault, Nicolas
Ben, Robert N.
Small-Molecule Ice Recrystallization Inhibitors Improve the Post-Thaw Function of Hematopoietic Stem and Progenitor Cells
title Small-Molecule Ice Recrystallization Inhibitors Improve the Post-Thaw Function of Hematopoietic Stem and Progenitor Cells
title_full Small-Molecule Ice Recrystallization Inhibitors Improve the Post-Thaw Function of Hematopoietic Stem and Progenitor Cells
title_fullStr Small-Molecule Ice Recrystallization Inhibitors Improve the Post-Thaw Function of Hematopoietic Stem and Progenitor Cells
title_full_unstemmed Small-Molecule Ice Recrystallization Inhibitors Improve the Post-Thaw Function of Hematopoietic Stem and Progenitor Cells
title_short Small-Molecule Ice Recrystallization Inhibitors Improve the Post-Thaw Function of Hematopoietic Stem and Progenitor Cells
title_sort small-molecule ice recrystallization inhibitors improve the post-thaw function of hematopoietic stem and progenitor cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044699/
https://www.ncbi.nlm.nih.gov/pubmed/30023498
http://dx.doi.org/10.1021/acsomega.6b00178
work_keys_str_mv AT briardjennieg smallmoleculeicerecrystallizationinhibitorsimprovethepostthawfunctionofhematopoieticstemandprogenitorcells
AT jahansuria smallmoleculeicerecrystallizationinhibitorsimprovethepostthawfunctionofhematopoieticstemandprogenitorcells
AT chandranpriya smallmoleculeicerecrystallizationinhibitorsimprovethepostthawfunctionofhematopoieticstemandprogenitorcells
AT allandavid smallmoleculeicerecrystallizationinhibitorsimprovethepostthawfunctionofhematopoieticstemandprogenitorcells
AT pineaultnicolas smallmoleculeicerecrystallizationinhibitorsimprovethepostthawfunctionofhematopoieticstemandprogenitorcells
AT benrobertn smallmoleculeicerecrystallizationinhibitorsimprovethepostthawfunctionofhematopoieticstemandprogenitorcells