Identification of Human Mononuclear Leukocytes Bearing Receptors for Somatostatin and Glucagon

Author:

Bhathena Sam J1,Louie James2,Schechter Geraldine P3,Redman Robert S4,Wahl Larry2,Recant Lillian1

Affiliation:

1. Diabetes Research Laboratory, Veterans Administration Medical Center Washington, D.C.

2. Laboratory of Microbiology and Immunology, National Institute of Dental Research, National Institutes of Health Bethesda, Maryland

3. Hematology Research Laboratory, Veterans Administration Medical Center Washington, D.C.

4. Oral Pathology Research Laboratory, Veterans Administration Medical Center Washington, D.C.

Abstract

Mononuclear leukocytes (MNL) were isolated from human blood by Ficoll-Hypaque. These cells were further separated into lymphocyte (L) and monocyte (M) enriched fractions. L contained 99% lymphocytes and M contained 74% monocytes, a threefold enrichment over MNL. Specific binding of somatostatin, glucagon, and insulin was measured in the three fractions. Binding of all three hormones in the M fraction was increased by a factor of 3 compared with MNL and was linear with cell number. Binding of glucagon and insulin to the L fraction was very low while, in contrast, somatostatin binding was substantial and linear with lymphocyte number. Autoradiography confirmed the binding of glucagon to monocytes and of somatostatin to both monocytes and lymphocytes. Somatostatin is the first of the peptide hormones shown to bind to both types of circulating mononuclear cells, perhaps complicating quantification of somatostatin binding in disease states in which differential alteration of binding to lymphocytes or monocytes might occur.

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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