| 1. The origins, maturation sequence, and traffic patterns
of azurocytes (AZ) were studied in vivo in the meadow vole (Microtus pennsylvanicus)
with the aid of various biological response modifiers. 2. AZ originated from
lymphocyte-like precursors in the bone marrow. These precursors entered into intense
mitotic activity in the bone marrow following progestin treatment. 3. While still in the
bone marrow, AZ precursors differentiated into granulated cells with some of the
histochemical properties of AZ. 4. At this time, maturation could be blocked completely
with cyclophosphamide. Hydroxyurea and cyclosporin A inhibited maturation significantly,
but did not block it. 5. Estradiol, hydrocortisone, prostaglandin E-2, and conditioned
medium had no effect on the numbers of cells induced. 6. Transitional stages between a
granulated bone marrow precursor and an AZ were rarely observed, suggesting rapid
synthesis of AZ inclusions upon terminal differentiation. 7. After release from the bone
marrow, AZ were common in the blood only. Modest numbers of cells were also found in the
red pulp of the spleen, and the thymic cortex. 8. AZ in the thymus were sometimes found in
clusters, and were often associated with septa. Very low numbers of mature AZ were
detected in the bone marrow. 9. AZ were absent from lymph nodes and Peyers patches, and
were never observed in the B-lymphocyte areas of the spleen. 10. Based on experiments with
dextran sulphate, AZ and their precursors never entered the recirculating lymphocyte
population. AZ in the blood or tissues were never observed in mitosis, and were never
observed degranulating. 11. Cyclophosphamide or hydrocortisone had no effect on AZ numbers
when administered at the peak of their occurrence in the blood. 12. Although no clear
function of the AZ was elucidated, experiments confirmed a high degree of similarity
between its properties and those of cytotoxic cells found in other mammals. |