Inositol 1,4,5-trisphosphate synthesis in mononuclear white blood cells of malignant hyperthermia-susceptible and normal human beings, following in vitro exposure to halothane, caffeine and ryanodine

2000 ◽  
Vol 17 (6) ◽  
pp. 364-372 ◽  
Author(s):  
U. Martens ◽  
T. Krause ◽  
J. Scholz ◽  
F. Wappler ◽  
K. Steinrücke ◽  
...  
1998 ◽  
Vol 95 ◽  
pp. 41
Author(s):  
B. Marczynski ◽  
M. Peel ◽  
P. Rozynek ◽  
J. Elliehausen ◽  
M. Korn ◽  
...  

1974 ◽  
Vol 20 (9) ◽  
pp. 1209-1218 ◽  
Author(s):  
E. Mankiewicz ◽  
V. Kurti ◽  
H. Adomonis

Suspensions of mycobacteriophages added to cultures of white blood cells (WBC's) reduce the phytohaemagglutinin (PHA) stimulated blast responses. Ultraviolet (UV) inactivation of the phages abolishes the inhibitory effect. Buffy coat cells from guinea pigs inoculated with mycobacteriophages and mice inoculated with these phages or with lysogenic mycobacteria show, without prior in vitro exposure to the antigen, significant reductions in the rate of their migration. This "spontaneous" migration inhibition is removed by prior treatment of the cells with trypsin or puromycin.


Blood ◽  
1971 ◽  
Vol 37 (2) ◽  
pp. 136-141 ◽  
Author(s):  
JOHN E. KURNICK ◽  
WILLIAM A. ROBINSON

Abstract Peripheral blood from normal humans and patients with circulating atypical mononuclear cells have been studied for their ability to form granulocytic colonies in vitro in the agar-gel method of hematopoietic cell culture. WBC from patients with chronic lymphocytic leukemia failed to proliferate. Normal human white blood cells gave rise to 0.5-8 colonies per 1 x 106 cells plated, while peripheral blood containing large mononuclear cells gave rise to 15 to 120 colonies per 1 x 106 cells plated, depending upon the number of such cells plated. Colonies averaged 500 cells in size by day 20 of culture and appeared to be granulocytic.


Blood ◽  
1971 ◽  
Vol 38 (4) ◽  
pp. 500-508 ◽  
Author(s):  
WILLIAM A. ROBINSON ◽  
JOHN E. KURNICK ◽  
BEVERLEY L. PIKE

Abstract The colony-forming potential of peripheral white blood cells from patients with acute leukemia on normal human peripheral WBC feeder layers has been studied. White blood cells from 12 of 20 patients with acute granulocytic leukemia gave rise to large numbers of colonies, while WBC from eight patients with AGL, four patients with acute lymphocytic leukemia and three patients with acute stem cell leukemia gave rise to no colonies or only small numbers. Colonies formed from WBC of patients with AGL appear to go through a process of morphologic maturation to segmented granulocyte forms. Leukemic WBC will not serve as feeder layers in this system, but are not inhibitory in this respect. The significance of these findings is discussed.


PEDIATRICS ◽  
1973 ◽  
Vol 51 (2) ◽  
pp. 230-233
Author(s):  
Andrew A. Raubitschek ◽  
Alan S. Levin ◽  
Daniel P. Stites ◽  
Edward B. Shaw ◽  
H. Hugh Fudenberg

An 8-year-old boy with chronic granulomatous disease (CGD) was admitted in moribund condition with aspergillus pneumonia. Because of the gravity of the situation, normal granulocyte infusions were used as adjuncts to the more conventional antimicrobial therapy. White blood cells, derived from a total of 58 units of whole blood obtained by leukophoresis of the father, were given in two separate doses. The first dose, totaling 2.8 x 1010 granulocytes, was coincident with significant improvement, and the second, totaling 3.0 x 1010 granulocytes, was coincident with the onset of clinical improvement and interim recovery. Transient improvement in in vitro granulocyte function was noted in cells taken from the patient's blood immediately after infusion. No adverse effects of the infusions were noted in either the patient or the donor. Although it is impossible to divorce the therapeutic effect of the granulocyte infusions from the more conventional therapy, we conclude that normal granulocyte infusions can be considered a valid adjunct in children with CGD who are suffering from a life-threatening infection.


2017 ◽  
Vol 38 (6) ◽  
pp. 500-508 ◽  
Author(s):  
Edel Noriega-Álvarez ◽  
Guillermo A. Martínez Pimienta ◽  
Ana M. Benítez Segura ◽  
María T. Bajén Lázaro ◽  
Alba Rodríguez-Gasén ◽  
...  

1987 ◽  
Author(s):  
L Mannucci ◽  
R Redaelli ◽  
E Tremoll

To evaluate the effects of blood cells on the response of platelets to aggregating agents using whole blood impedance aggregometer, studies were carried out on whole blood (WB) of normal subjects and of patients with: polycythemia vera (PV), iatrogenic anemia (IA), primary thrombocytosis (PT), idiopathic thrombotic purpura (ITP), myeloid chronic leukemia (MCL), iatrogenic leukopenia (IL). The in vitro effects of red blood cells (RBC) and of white blood cells (WBC) on platelet rich plasma (PRP) aggregation were also evaluated. WB, PRP, WBC and RBC were prepared by conventional methods. Aggregation was performed using the impedance aggregometer (mod. 540, Chrono Log Corp). In normal subjects the concentration of collagen giving 50 % aggregation (AC50 ) found in PRP did not differ from that of WB, indicating that hematocrit values within the normal range did not appreciably affect platelet aggregation. The results obtained in WB of patients are summarized in the table: In vitro data showed that aggregation in prp in wb of normal subjects was related to the number of platelets present in the sample. RBC added to PRP significant reduced aggregation only when the RBC number was greater than 4.101 cells. No effect of WBC on collagen induced aggregation of PRP was observed, whereas significant inhibition was detected after ADP. It is concluded that the aggregation evaluated in WB with impedance method is dependent on the platelet number. Also, in vitro data and studies in WB of patients indicate that aggregation is significantly affected by the presence of cells other than platelets only in conditions of changes of the ratio between platelets and leukocytes and/or red cells.


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