Multivesicular bodies are an intermediate stage in the formation of platelet alpha-granules

Blood. 1998 Apr 1;91(7):2313-25.

Abstract

We have used ultrathin cryosectioning and immunogold cytochemistry to study the position of alpha-granules in the endocytic and biosynthetic pathways in megakaryocytes and platelets. Morphologically, we distinguished three types of granules; so-called multivesicular bodies type I (MVB I) with internal vesicles only, granules with internal vesicles and an electron dense matrix (MVB II), and the alpha-granules with mainly a dense content and often internal membrane vesicles at their periphery. The MVBs were prominent in cultured megakaryocytes and the megakaryoblastic cell line CHRF-288, but were less numerous in bone marrow megakaryocytes and platelets, whereas alpha-granules were most prominent in mature bone marrow megakaryocytes and in platelets. The internalization kinetics of bovine serum albumin-gold particles and of fibrinogen positioned the MVB subtypes and alpha-granules sequentially in the endocytic pathway. MVBs contained the secretory proteins von Willebrand factor (vWF) and beta-thromboglobulin (beta-TG), the platelet-specific membrane protein P-selectin, and the lysosomal membrane protein CD63. Within the MVBs, endocytosed fibrinogen and endogenous beta-TG were restricted to the matrix, while vWF was predominantly associated with internal vesicles. CD63 was also observed in association with internal membrane vesicles in the alpha-granules. These observations, and the gradual morphologic transition from granules containing vesicles to granules containing predominantly dense material, suggest that MVBs represent a developmental stage in alpha-granule maturation.

MeSH terms

  • Animals
  • Blood Platelets / metabolism
  • Blood Platelets / ultrastructure*
  • Cattle
  • Cells, Cultured
  • Cytoplasmic Granules / metabolism
  • Cytoplasmic Granules / ultrastructure*
  • Endocytosis*
  • Humans
  • Immunohistochemistry
  • Megakaryocytes / metabolism
  • Megakaryocytes / ultrastructure
  • Microscopy, Electron
  • Serum Albumin, Bovine / metabolism

Substances

  • Serum Albumin, Bovine