Niche Extracellular Matrix Components and Their Influence on HSC

J Cell Biochem. 2017 Aug;118(8):1984-1993. doi: 10.1002/jcb.25905. Epub 2017 Apr 24.

Abstract

Maintenance of hematopoietic stem cells (HSC) takes place in a highly specialized microenvironment within the bone marrow. Technological improvements, especially in the field of in vivo imaging, have helped unravel the complexity of the niche microenvironment and have completely changed the classical concept from what was previously believed to be a static supportive platform, to a dynamic microenvironment tightly regulating HSC homeostasis through the complex interplay between diverse cell types, secreted factors, extracellular matrix molecules, and the expression of different transmembrane receptors. To add to the complexity, non-protein based metabolites have also been recognized as a component of the bone marrow niche. The objective of this review is to discuss the current understanding on how the different extracellular matrix components of the niche regulate HSC fate, both during embryonic development and in adulthood. Special attention will be provided to the description of non-protein metabolites, such as lipids and metal ions, which contribute to the regulation of HSC behavior. J. Cell. Biochem. 118: 1984-1993, 2017. © 2017 Wiley Periodicals, Inc.

Keywords: EXTRACELLULAR MATRIX MOLECULES; HEMATOPOIETIC STEM CELLS; INTEGRINS; LIPIDS; MEGAKARYOCYTES; METAL IONS; MICROENVIRONMENT; NICHE.

Publication types

  • Review

MeSH terms

  • Animals
  • Bone Marrow Cells / cytology
  • Bone Marrow Cells / metabolism*
  • Cellular Microenvironment / genetics*
  • Chemokine CXCL12 / genetics
  • Chemokine CXCL12 / metabolism
  • Dinoprostone / metabolism
  • Embryo, Mammalian
  • Embryonic Development / genetics
  • Extracellular Matrix / chemistry*
  • Extracellular Matrix / genetics
  • Extracellular Matrix / metabolism
  • Extracellular Matrix Proteins / genetics*
  • Extracellular Matrix Proteins / metabolism
  • Gene Expression Regulation
  • Hematopoietic Stem Cells / cytology
  • Hematopoietic Stem Cells / metabolism*
  • Homeostasis
  • Humans
  • Receptors, CXCR4 / genetics
  • Receptors, CXCR4 / metabolism
  • Signal Transduction
  • Stem Cell Niche / genetics*

Substances

  • CXCL12 protein, human
  • CXCR4 protein, human
  • Chemokine CXCL12
  • Extracellular Matrix Proteins
  • Receptors, CXCR4
  • Dinoprostone