Marked reduction of spectrinin hereditary spherocytosis in the common house mouse

Blood. 1978 Jun;51(6):1149-55.

Abstract

In contrast to the disease in humans, hereditary spherocytosis in the common house mouse produces an extreme spherocytosis. The cells show a broad distribution in size ranging from microcytic to macrocytic. Of particular interest is the finding of a substantial reduction in the major membrane polypeptide called spectrin, supporting a critical role for this protein in the control of erythrocyte shape and membrane stability.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Electrophoresis, Polyacrylamide Gel
  • Erythrocyte Membrane
  • Membrane Proteins / deficiency*
  • Mice
  • Peptides
  • Spectrin / deficiency*
  • Spherocytes
  • Spherocytosis, Hereditary / blood*
  • Spherocytosis, Hereditary / genetics

Substances

  • Membrane Proteins
  • Peptides
  • Spectrin