CD44 is dispensable for B lymphopoiesis

Immunol Lett. 2004 Aug 15;95(1):71-5. doi: 10.1016/j.imlet.2004.06.004.

Abstract

Several studies have implicated a role for the cell surface glycoprotein CD44 in lymphocyte differentiation, adhesion to the matrix, homing, activation and apoptosis. However, the requirement of CD44 in B cell maturation remains elusive. To address this point, we analyzed the generation and activation of B lymphocytes in CD44-deficient mice. Unexpectedly, both maturation and autoreconstitution of early bone marrow B cell progenitors after sublethal irradiation as well as frequencies of splenic B cell subsets are indistinguishable in wild-type and CD44-deficient mice. Furthermore, splenic CD44-deficient B lymphocytes show a normal activation pattern after stimulation with LPS, anti-IgM/IL-4 or anti-CD40/IL-4. These results show for the first time that CD44 is clearly dispensable for development, reconstitution and activation of B lymphocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Differentiation, B-Lymphocyte / metabolism
  • B-Lymphocyte Subsets / immunology
  • B-Lymphocytes / immunology*
  • Bone Marrow Cells / cytology
  • Hyaluronan Receptors / physiology*
  • Lymphocyte Activation
  • Lymphopoiesis*
  • Mice
  • Mice, Knockout
  • Spleen / cytology

Substances

  • Antigens, Differentiation, B-Lymphocyte
  • Hyaluronan Receptors