Common-Lymphoid-Progenitor-Independent Pathways of Innate and T Lymphocyte Development

Cell Rep. 2016 Apr 19;15(3):471-480. doi: 10.1016/j.celrep.2016.03.039. Epub 2016 Apr 7.

Abstract

All lymphocytes are thought to develop from common lymphoid progenitors (CLPs). However, lymphoid-primed multipotent progenitors (LMPPs) are more efficient than CLPs in differentiating into T cells and group 2 innate lymphoid cells (ILC2s). Here, we have divided LMPPs into CD127(-) (LMPP-s) and CD127(+) (LMPP+s) subsets and compared them with Ly6D(-) and Ly6D(+) CLPs. Adult LMPP+s differentiated into T cells and ILCs more rapidly and efficiently than other progenitors in transplantation assays. The development of T cells and ILC2s is highly active in the neonatal period. Neonatal CLPs are rare and, unlike prominent neonatal LMPP+s, do not efficiently differentiate into T cells and ILC2s. ILC2s generated in the neonatal period are long lived and persist in adult tissues. These results suggest that some ILCs and T cells may develop from LMPP+s via CLP-independent pathways.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Bone Marrow / metabolism
  • Cell Lineage
  • Gene Expression Profiling
  • Immunity, Innate*
  • Lung / cytology
  • Lymphocyte Subsets / cytology
  • Lymphocyte Subsets / metabolism
  • Lymphoid Progenitor Cells / metabolism*
  • Mice, Inbred C57BL
  • Signal Transduction*
  • Spleen / cytology
  • T-Lymphocytes / cytology*
  • T-Lymphocytes / metabolism*