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Evidence for glucocorticoid receptor in human leukocytes
Acta Physiologica Scandinavica
|October 1, 1976
Summary
Human leukocytes show saturable and non-saturable glucocorticoid uptake. The saturable component suggests a specific glucocorticoid receptor, particularly in chronic lymphatic leukemia cells.
Area of Science:
- Biochemistry
- Cell Biology
- Immunology
Background:
- Glucocorticoids are crucial hormones with diverse physiological effects.
- Understanding glucocorticoid uptake mechanisms is vital for pharmacology and disease research.
- Leukocytes play a key role in immune responses and are targets for glucocorticoid therapy.
Purpose of the Study:
- To investigate the in vitro uptake of glucocorticoids by human peripheral leukocytes.
- To characterize the components of glucocorticoid uptake in these cells.
- To determine if human leukocyte glucocorticoid uptake involves specific receptors, similar to those in other species.
Main Methods:
- In vitro incubation of human peripheral leukocytes with glucocorticoids.
- Analysis of uptake kinetics, including saturable and non-saturable components.
- Comparison of human leukocyte uptake with known glucocorticoid receptor characteristics in rabbit granulocytes.
- Study of glucocorticoid uptake in cells from patients with chronic lymphatic leukemia and chronic myeloid leukemia.
Main Results:
- Human peripheral leukocyte glucocorticoid uptake comprises both saturable and non-saturable components.
- The saturable component exhibits characteristics (structural specificity, time course, metabolic sensitivity, half-saturation concentration) consistent with a specific glucocorticoid receptor.
- Cells from chronic lymphatic leukemia demonstrated saturable glucocorticoid uptake, while chronic myeloid leukemia cells did not.
Conclusions:
- Human peripheral leukocytes possess a specific glucocorticoid receptor mediating saturable uptake.
- This receptor shares similarities with the known glucocorticoid receptor in rabbit granulocytes.
- Saturable glucocorticoid uptake is present in chronic lymphatic leukemia cells but not in chronic myeloid leukemia cells, suggesting differential receptor expression or function in these leukemias.