Re-entering the pluripotent state from blood lineage: promises and pitfalls of blood reprogramming

FEBS Lett. 2019 Dec;593(23):3244-3252. doi: 10.1002/1873-3468.13659. Epub 2019 Nov 26.

Abstract

Blood reprogramming, in which induced pluripotent stem cells (iPSCs) are derived from haematopoietic lineages, has rapidly advanced over the past decade. Since the first report using human blood, haematopoietic cell types from various sources, such as the peripheral bone marrow and cord blood, have been successfully reprogrammed. The volume of blood required has also decreased, from around tens of millilitres to a single finger-prick drop. Besides, while early studies were limited to reprogramming methods relying on viral integration, nonintegrating reprogramming systems for blood lineages have been subsequently established. Together, these improvements have made feasible the future clinical applications of blood-derived iPSCs. Here, we review the progress in blood reprogramming from various perspectives, including the starting materials and subsequent reprogramming strategies. We also discuss the downstream applications of blood-derived iPSCs, highlighting their clinical value in terms of disease modelling and therapeutic development.

Keywords: blood; cord blood; iPSC derivation; integrating reprogramming strategies; nonintegrating reprogramming strategies; peripheral blood; pluripotency; reprogramming; translational applications.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Blood Cells / metabolism*
  • Bone Marrow Cells / metabolism
  • Cell Differentiation / genetics
  • Cell Lineage / genetics
  • Cellular Reprogramming / genetics*
  • Fetal Blood / cytology
  • Fetal Blood / metabolism
  • Hematopoietic Stem Cells / cytology
  • Hematopoietic Stem Cells / metabolism*
  • Humans
  • Induced Pluripotent Stem Cells / metabolism*