Comparison and correlation among in vitro and in vivo assays to assess cord blood quality according to delivery temperature and time after collection

Transfus Apher Sci. 2019 Aug;58(4):475-483. doi: 10.1016/j.transci.2019.05.006. Epub 2019 May 22.

Abstract

Cord blood (CB) has been used as an alternative source for unrelated allogeneic hematopoietic stem cell transplantation. To determine which assay was useful for predicting the successful outcome of CB transplantation, CBs were grouped according to the temperature (4 °C, 24 °C, and 37 °C) and time (24, 48, and 72 h) after collection. The viability, early apoptosis, and colony forming units (CFUs) were ascertained for the total nucleated cells (TNCs) and CD34+ cells; in addition, the engraftment of infused CD34+ cells in NSG mice was determined. The viability of the TNCs and CD34+ cells and total CFUs were significantly decreased whereas the early apoptosis was significantly increased in the 72 h group at 37 °C compared to that of the 24 h group at 24 °C. The viability and early apoptosis of the TNCs correlated with those of CD34+ cells. In addition, the viability and early apoptosis correlated with the number of granulocyte/monocyte progenitor CFUs. In transplanted NSG mice, the frequency of human CD45+ cells decreased in the 72 h group at 24 °C compared to that of the 24 h group at 24 °C and was negatively correlated with early apoptosis of TNCs and CD34+ cells. This study demonstrated that the early apoptosis of TNCs and CD34+ cells constitutes a useful marker for predicting the engraftment of HSCs and may provide helpful data for standard assessment regarding CB quality by analyzing the correlation between in vitro and in vivo assays using NSG mice.

Keywords: Colony forming unit; Cord blood; Early apoptosis; Hematopoietic stem cell; Viability.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Apoptosis
  • Biological Assay*
  • Cord Blood Stem Cell Transplantation
  • Fetal Blood* / cytology
  • Fetal Blood* / metabolism
  • Hematopoietic Stem Cells* / cytology
  • Hematopoietic Stem Cells* / metabolism
  • Heterografts
  • Humans
  • Mice
  • Mice, Knockout