Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1982 Sep;35(9):967-71.
doi: 10.1136/jcp.35.9.967.

Relation of neutrophil alkaline phosphatase activity to Fc IgG receptor development in human blood and bone marrow

Relation of neutrophil alkaline phosphatase activity to Fc IgG receptor development in human blood and bone marrow

C S Scott et al. J Clin Pathol. 1982 Sep.

Abstract

A possible correlation between Fc-IgG receptor expression and neutrophil alkaline phosphatase (NAP) activity was investigated in relation to maturation of granulocytes in human peripheral blood and bone marrow. NAP activity was studied in bone marrow from patients with normal peripheral blood NAP scores (20-100) and compared with those with high NAP scores. Results indicate that NAP activity is confined to segmented neutrophils (SN) in marrow and peripheral blood except when peripheral NAP activity is abnormally high. There is a normal increase of approximately 60% in mean NAP scores of peripheral blood compared to marrow SN. Granulocyte Fc-IgG receptor activity, known to increase with maturation, was studied in relation to NAP activity. A combined assay using a rosetting technique with ox-erythrocyte (oxE) antibody-IgG and subsequent NAP cytochemistry was used. Receptor expression was found to be virtually complete in normal granulocytic maturation before the appearance of detectable NAP activity. This was supported by findings in chronic myeloid leukaemia where no cases of low Fc receptor activity were found despite NAP scores of less than 5. The significance of these findings is discussed in the light of current concepts of the control of NAP activity.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Br J Haematol. 1975 Nov;31(3):371-9 - PubMed
    1. J Lab Clin Med. 1965 Apr;65:698-705 - PubMed
    1. J Clin Pathol. 1980 Jun;33(6):555-61 - PubMed
    1. Proc Soc Exp Biol Med. 1973 May;143(1):212-7 - PubMed
    1. Clin Exp Immunol. 1979 Nov;38(2):300-5 - PubMed