The azurocyte: a new kind of leukocyte from wild voles (Microtus)

1987 ◽  
Vol 65 (1) ◽  
pp. 54-62 ◽  
Author(s):  
Steve Mihok ◽  
Jean-Paul Descôteaux ◽  
Todd Lawton ◽  
Anya Lobreau ◽  
Bill Schwartz

We have identified a new mammalian leukocyte from voles (Cricetidae, Microtus). This "azurocyte" is a large mononuclear cell with numerous cytoplasmic inclusions that stain purple with azure dyes. The cell resembles a young lymphocyte with numerous mitochondria, a prominent Golgi complex, and modest amounts of rough endoplasmic reticulum. The inclusions are homogeneous, membrane-bound, electron-dense bodies that contain a highly acidic, sulphated glycosaminoglycan, glycoprotein, nonspecific esterase, β-glucuronidase, and an aminopeptidase. Azurocytes are common in adult voles, particularly pregnant females, and can be induced artificially with progesterone. In humans (large granular lymphocyte) and in guinea pigs (Kurloff cell), morphologically distinct cells with azurophilic inclusions have been associated with natural killer activity. The vole azurocyte may therefore be a similar leukocyte with special functions during pregnancy.

Blood ◽  
1983 ◽  
Vol 62 (3) ◽  
pp. 627-634 ◽  
Author(s):  
M Palutke ◽  
L Eisenberg ◽  
J Kaplan ◽  
M Hussain ◽  
K Kithier ◽  
...  

Abstract A patient with low-grade lymphocytosis, splenomegaly, and neutropenia, but adequate myeloid leukogenesis, was found to have chronic lymphocytic leukemia, which represented a clonal proliferation of a distinct T-lymphocyte subset. The lymphocytes did not form E rosettes but had an OKT3+, OKT4+, OKT6+, OKT8+, OKT11+, HNK-1+, HNK-36+, OKIa1+, OKM1+ phenotype and functionally had suppressor and natural killer activity. Morphologically, they were large granular lymphocytes, which were strongly acid phosphatase positive and nonspecific esterase negative. They did not respond to mitogens, or to allogeneic cells. Initially, the spleen appeared to be the most involved organ and, judging from the high proportion of leukemic splenic lymphocytes in the S and G2/M phases of the cell cycle, was also the organ of origin of the leukemic cells. Only a few leukemic cells in the blood and bone marrow were in S and G2/M phases. After splenectomy, the lymphocyte count rose considerably and the bone marrow became progressively more infiltrated by tumor nodules. One year after diagnosis, the patient was started on chemotherapy because of progressive anemia. He responded to the chemotherapy by normalization of the hemoglobin and neutrophil count and had a moderate decrease in the bone marrow involvement and peripheral lymphocytosis.


Blood ◽  
1983 ◽  
Vol 62 (3) ◽  
pp. 627-634
Author(s):  
M Palutke ◽  
L Eisenberg ◽  
J Kaplan ◽  
M Hussain ◽  
K Kithier ◽  
...  

A patient with low-grade lymphocytosis, splenomegaly, and neutropenia, but adequate myeloid leukogenesis, was found to have chronic lymphocytic leukemia, which represented a clonal proliferation of a distinct T-lymphocyte subset. The lymphocytes did not form E rosettes but had an OKT3+, OKT4+, OKT6+, OKT8+, OKT11+, HNK-1+, HNK-36+, OKIa1+, OKM1+ phenotype and functionally had suppressor and natural killer activity. Morphologically, they were large granular lymphocytes, which were strongly acid phosphatase positive and nonspecific esterase negative. They did not respond to mitogens, or to allogeneic cells. Initially, the spleen appeared to be the most involved organ and, judging from the high proportion of leukemic splenic lymphocytes in the S and G2/M phases of the cell cycle, was also the organ of origin of the leukemic cells. Only a few leukemic cells in the blood and bone marrow were in S and G2/M phases. After splenectomy, the lymphocyte count rose considerably and the bone marrow became progressively more infiltrated by tumor nodules. One year after diagnosis, the patient was started on chemotherapy because of progressive anemia. He responded to the chemotherapy by normalization of the hemoglobin and neutrophil count and had a moderate decrease in the bone marrow involvement and peripheral lymphocytosis.


Cytometry ◽  
1998 ◽  
Vol 32 (4) ◽  
pp. 280-285 ◽  
Author(s):  
Loris Zamai ◽  
Adriana R. Mariani ◽  
Giorgio Zauli ◽  
Luigi Rodella ◽  
Rita Rezzani ◽  
...  

1989 ◽  
Vol 15 ◽  
pp. 194
Author(s):  
H.S. Wang ◽  
M. Kariya ◽  
H. Kanzaki ◽  
M. Yoshida ◽  
M. Tokushige ◽  
...  

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