IN VITRO GLUCOCORTICOID-SENSITIVITY OF LECTIN-DRIVEN LYMPHOCYTE DNA-SYNTHESIS AFTER RECOVERY FROM SEVERE MAJOR DEPRESSION.

1992 ◽  
Vol 15 ◽  
pp. 128B
Author(s):  
N Wodarz ◽  
R Rupprecht ◽  
J Kornhuber ◽  
B Schmitz ◽  
K Wild ◽  
...  
Nature ◽  
1969 ◽  
Vol 224 (5225) ◽  
pp. 1207-1208 ◽  
Author(s):  
J. F. MOORHEAD ◽  
E. PARASKOVA-TCHERNOZENSKA ◽  
A. J. PIRRIE ◽  
C. HAYES

1983 ◽  
Vol 39 (2) ◽  
pp. 630-637 ◽  
Author(s):  
H R Rubin ◽  
R U Sorensen ◽  
P A Chase ◽  
J D Klinger

1983 ◽  
Vol 71 (1) ◽  
pp. 126
Author(s):  
C SERIO ◽  
R FREDERICK ◽  
L MANSFIELD ◽  
L PENNEY ◽  
G LECHUGA

Dermatology ◽  
1984 ◽  
Vol 169 (1) ◽  
pp. 18-22
Author(s):  
A.L. Claudy ◽  
O. de Bouteiller ◽  
J.L. Touraine

Blood ◽  
1969 ◽  
Vol 33 (2) ◽  
pp. 300-312 ◽  
Author(s):  
SYDNEY E. SALMON ◽  
H. HUGH FUDENBERG

Abstract Twenty-six patients with multiple myeloma and macroglobulinemia of Waldenström were studied clinically and immunologically with characterization of their paraproteins and normal immunoglobulins, as well as by in vitro culture of their peripheral lymphocytes for evaluation of DNA and RNA synthesis after phytohemagglutinin stimulation. The lymphocytes of the patients were found to be significantly deficient in response to PHA as compared to normals and patients with benign hypergammaglobulinemia. Levels of normal immunoglobulins were reduced in almost all of the paraproteinemic patients, but there was not a direct correlation between lymphocyte unresponsiveness and immunoglobulin deficiency. The defect in lymphocyte function appeared to be cellular inasmuch as normal lymphocytes had normal DNA synthesis when cultured in myeloma plasma. The decrease in lymphocyte nucleic acid synthesis appeared to be unrelated to immunoglobulin class, quantitative levels or antigenic characteristics of the patients’ paraproteins. Untreated myeloma patients with a past history of infection had lower levels of lymphocyte DNA synthesis than those patients who lacked such a history, suggesting a relationship between the in vitro lymphocyte response to PHA and the in vivo response to the antigenic challenge of bacterial infection.


2001 ◽  
Vol 59 (3) ◽  
pp. 905-912
Author(s):  
William G. Couser ◽  
Jeffrey W. Pippin ◽  
Stuart J. Shankland

1979 ◽  
Author(s):  
K. L. Kellar ◽  
B. L. Evatt ◽  
C. R. McGrath ◽  
R. B. Ramsey

Liquid cultures of bone marrow cells enriched for megakaryocytes were assayed for incorporation of 3H-thymidine (3H-TdR) into acid-precipitable cell digests to determine the effect of thrombopoietin on DNA synthesis. As previously described, thrombopoietin was prepared by ammonium sulfate fractionation of pooled plasma obtained from thrombocytopenic rabbits. A control fraction was prepared from normal rabbit plasma. The thrombopoietic activity of these fractions was determined in vivo with normal rabbits as assay animals and the rate of incorporation of 75Se-selenomethionine into newly formed platelets as an index of thrombopoietic activity of the infused material. Guinea pig megakaryocytes were purified using bovine serum albumin gradients. Bone marrow cultures containing 1.5-3.0x104 cells and 31%-71% megakaryocytes were incubated 18 h in modified Dulbecco’s MEM containing 10% of the concentrated plasma fractions from either thrombocytopenic or normal rabbits. In other control cultures, 0.9% NaCl was substituted for the plasma fractions. 3H-TdR incorporation was measured after cells were incubated for 3 h with 1 μCi/ml. The protein fraction containing thrombopoietin-stimulating activity caused a 25%-31% increase in 3H-TdR incorporation over that in cultures which were incubated with the similar fraction from normal plasma and a 29% increase over the activity in control cultures to which 0.9% NaCl had been added. These data suggest that thrombopoietin stimulates DNA synthesis in megakaryocytes and that this tecnique may be useful in assaying thrombopoietin in vitro.


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