The human chorion contains definitive hematopoietic stem cells from the fifteenth week of gestation

Development. 2017 Apr 15;144(8):1399-1411. doi: 10.1242/dev.138438. Epub 2017 Mar 2.

Abstract

We examined the contribution of the fetal membranes, amnion and chorion, to human embryonic and fetal hematopoiesis. A population of cells displaying a hematopoietic progenitor phenotype (CD34++ CD45low) of fetal origin was present in the chorion at all gestational ages, associated with stromal cells or near blood vessels, but was absent in the amnion. Prior to 15 weeks of gestation, these cells lacked hematopoietic in vivo engraftment potential. Differences in the chemokine receptor and β1 integrin expression profiles of progenitors between the first and second trimesters suggest that these cells had gestationally regulated responses to homing signals and/or adhesion mechanisms that influenced their ability to colonize the stem cell niche. Definitive hematopoietic stem cells, capable of multilineage and long-term reconstitution when transplanted in immunodeficient mice, were present in the chorion from 15-24 weeks gestation, but were absent at term. The second trimester cells also engrafted secondary recipients in serial transplantation experiments. Thus, the human chorion contains functionally mature hematopoietic stem cells at mid-gestation.

Keywords: Chorion; Extraembryonic development; Hematopoietic development; Human hematopoietic stem cells.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / metabolism
  • Cell Adhesion Molecules / metabolism
  • Cell Count
  • Cell Lineage
  • Chorion / cytology*
  • Chorion / transplantation
  • Chorionic Villi / metabolism
  • Collagenases / metabolism
  • Female
  • Fetus / cytology
  • Hematopoietic Stem Cells / cytology*
  • Humans
  • Integrin beta1 / metabolism
  • Mice, SCID
  • Phenotype
  • Pregnancy
  • Pregnancy Trimesters / metabolism
  • Receptors, Chemokine / metabolism
  • Trypsin / metabolism

Substances

  • Antigens, CD
  • Cell Adhesion Molecules
  • Integrin beta1
  • Receptors, Chemokine
  • Trypsin
  • Collagenases