The Bioactive Peptide SL-13R Expands Human Umbilical Cord Blood Hematopoietic Stem and Progenitor Cells In Vitro.
Animals
Antigens, CD34
/ metabolism
Biomarkers
Carrier Proteins
Cell Culture Techniques
Cell Differentiation
Cell Self Renewal
Cells, Cultured
Fetal Blood
/ cytology
Fluorescent Antibody Technique
Hematopoietic Stem Cell Transplantation
Hematopoietic Stem Cells
/ cytology
Humans
Immunophenotyping
Mice
Peptides
/ pharmacology
Protein Binding
cell culture
hematopoietic stem/progenitor cell
peptide
umbilical cord blood
Journal
Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009
Informations de publication
Date de publication:
01 Apr 2021
01 Apr 2021
Historique:
received:
05
02
2021
revised:
27
02
2021
accepted:
02
03
2021
entrez:
30
4
2021
pubmed:
1
5
2021
medline:
25
5
2021
Statut:
epublish
Résumé
Hematopoietic stem and progenitor cell (HSPC) transplantation is a curative treatment of hematological disorders that has been utilized for several decades. Although umbilical cord blood (UCB) is a promising source of HSPCs, the low dose of HSPCs in these preparations limits their use, prompting need for ex vivo HSPC expansion. To establish a more efficient method to expand UCB HSPCs, we developed the bioactive peptide named SL-13R and cultured UCB HSPCs (CD34+ cells) with SL-13R in animal component-free medium containing a cytokine cocktail. Following 9 days of culture with SL-13R, the numbers of total cells, CD34+, CD38- cells, and hematopoietic stem cell (HSC)-enriched cells were significantly increased relative to control. Transplantation of cells cultured with SL-13R into immunodeficient NOD/Shi-scid/IL-2Rγ knockout mice confirmed that they possess long-term reconstitution and self-renewal ability. AHNAK, ANXA2, and PLEC all interact with SL-13R. Knockdown of these genes in UCB CD34+ cells resulted in reduced numbers of hematopoietic colonies relative to SL-13R-treated and non-knockdown controls. In summary, we have identified a novel bioactive peptide SL-13R promoting expansion of UCB CD34+ cells with long-term reconstitution and self-renewal ability, suggesting its clinical use in the future.
Identifiants
pubmed: 33915948
pii: molecules26071995
doi: 10.3390/molecules26071995
pmc: PMC8036704
pii:
doi:
Substances chimiques
Antigens, CD34
0
Biomarkers
0
Carrier Proteins
0
Peptides
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Ministry of Education, Culture, Sports, Science and Technology
ID : 1082328
Organisme : Japan Agency for Medical Research and Development
ID : A188
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