Matrix metalloproteinases in stem cell mobilization

Matrix Biol. 2015 May-Jul:44-46:175-83. doi: 10.1016/j.matbio.2015.01.011. Epub 2015 Jan 21.

Abstract

Hematopoietic stem cells (HSCs) have the capability to migrate back and forth between their preferred microenvironment in bone marrow niches and the peripheral blood, but under steady-state conditions only a marginal number of stem cells can be found in the circulation. Different mobilizing agents, however, which create a highly proteolytic milieu in the bone marrow, can drastically increase the number of circulating HSCs. Among other proteases secreted and membrane-bound matrix metalloproteinases (MMPs) are known to be involved in the induced mobilization process and can digest niche-specific extracellular matrix components and cytokines responsible for stem cell retention to the niches. Iatrogenic stem cell mobilization and stem cell homing to their niches are clinically employed on a routine basis, although the exact mechanisms of both processes are still not fully understood. In this review we provide an overview on the various roles of MMPs in the induced release of HSCs from the bone marrow.

Keywords: extracellular matrix; hematopoietic stem cells; proteolytic microenvironment; stem cell homing; stem cell niche.

Publication types

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

MeSH terms

  • Animals
  • Cytokines / metabolism
  • Extracellular Matrix Proteins
  • Hematopoietic Stem Cell Mobilization*
  • Hematopoietic Stem Cells / cytology
  • Hematopoietic Stem Cells / physiology*
  • Humans
  • Matrix Metalloproteinases / metabolism*
  • Stem Cell Niche

Substances

  • Cytokines
  • Extracellular Matrix Proteins
  • Matrix Metalloproteinases