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Differential endocytosis of fluorescein iso-thiocyanate-concanavalin A by normal and chronic myeloid leukemic granulocytes.

Abstract
Isolated granulocytes from normal individuals and patients suffering from chronic myeloid leukemia (CML) displayed different fluorescent patterns on treatment with fluorescein isothiocyanate concanavalin A (Fl-Con A). The ligand was internalized by 86% of the normal granulocytes, while 80% of the leukemic granulocytes exhibited Fl-Con A localized on the cell periphery. In further experiments, pretreatment of the normal granulocytes with cytochalasin B, iodoacetamide, 2-deoxyglucose and sodium fluoride (but not with sodium azide or dinitrophenol) was found to drastically inhibit internalization of the ligand. However, pretreatment of granulocytes from CML patients with cytochalasin B and 2-deoxyglucose, caused only a little alteration in the pattern of Fl-Con A labelling relative to untreated cells. These results indicate that CML granulocytes are defective in their ability to endocytose Fl-Con A. We suggest that this differential interaction between Fl-Con A and normal and leukemic granulocytes is a convenient system to study the initial steps in receptor mediated endocytosis of Concanavalin A.
AuthorsS M Zingde, P N Anklesaria, S H Advani, A N Bhisey, B P Gothoskar
JournalBlut (Blut) Vol. 55 Issue 2 Pg. 81-8 (Aug 1987) ISSN: 0006-5242 [Print] Germany
PMID3475138 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Azides
  • Fluoresceins
  • fluorescein isothiocyanate-concanavalin A
  • Concanavalin A
  • Cytochalasin B
  • Sodium Fluoride
  • Sodium Azide
  • Fluorescein-5-isothiocyanate
  • Colchicine
  • Iodoacetamide
Topics
  • Azides (pharmacology)
  • Cell Differentiation
  • Cell Membrane (metabolism)
  • Colchicine (pharmacology)
  • Concanavalin A (analogs & derivatives, metabolism)
  • Cytochalasin B (pharmacology)
  • Endocytosis (drug effects)
  • Fluorescein-5-isothiocyanate (analogs & derivatives)
  • Fluoresceins (metabolism)
  • Granulocytes (cytology, drug effects, metabolism)
  • Histocytochemistry
  • Humans
  • Iodoacetamide (pharmacology)
  • Kinetics
  • Leukemia, Myeloid (blood, metabolism, physiopathology)
  • Sodium Azide
  • Sodium Fluoride (pharmacology)
  • Time Factors

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