Stimulation of aryl sulfatase in rat peritoneal macrophages exposed to bone in vitro

1981 ◽  
Vol 33 (1) ◽  
pp. 181-184 ◽  
Author(s):  
J. P. Gies ◽  
C. K. Dorey
Keyword(s):  
Peritoneal Macrophages ◽  
Aryl Sulfatase ◽  
Stimulation Of

scholarly journals Immunomodulatory Action of Triterpene Glycosides Isolated from the Sea Cucumber Actinocucumis typica. Structure-Activity Relationships

2014 ◽  
Vol 9 (6) ◽  
pp. 1934578X1400900 ◽  
Author(s):  
Evgeny A. Pislyagin ◽  
Dmitry L. Aminin ◽  
Alexandra S. Silchenko ◽  
Sergey A. Avilov ◽  
Pelageya V. Andryjashchenko ◽  
...  
Keyword(s):  
Peritoneal Macrophages ◽  
Triterpene Glycosides ◽  
Cytotoxic Activities ◽  
Ros Formation ◽  
Low Toxicity ◽  
Low Cytotoxicity ◽  
Immunomodulatory Action ◽  
Mouse Peritoneal Macrophages ◽  
Stimulation Of

Stimulation of lysosomal activity and ROS formation in mouse peritoneal macrophages by five triterpene glycosides, typicosides A1 (1), A2 (2), B1 (3), C1 (4) and C2 (5) has been studied and compared with their cytotoxic activities. Glycosides 1–3 possess moderate activities, but the most cytotoxic glycoside 5 is not active. Typicoside C1 (4), with low toxicity, was proved to be the most active concerning stimulation of ROS formation. This is the first example of a triterpene glycoside from sea cucumbers with low cytotoxicity, but which demonstrates a strong immunostimulatory effect on mouse peritoneal macrophages in vitro.

scholarly journals Immunomodulatory Activities of Dendrophthoe falcata (L.f) Ettingsh in Experimental Animals: In vitro and In vivo Investigations

2011 ◽  
Vol 3 (3) ◽  
pp. 619-630 ◽  
Author(s):  
S. P. Pattanayak ◽  
P. M. Mazumder
Keyword(s):  
Antibody Titer ◽  
Phagocytic Activity ◽  
Reticuloendothelial System ◽  
Peritoneal Macrophages ◽  
Immunomodulatory Activity ◽  
Hydroalcoholic Extract ◽  
Dendrophthoe Falcata ◽  
Stimulation Of

In the present study, an attempt was made to screen immunomodulatory activity of the hydroalcoholic extract (HEDF) of Dendrophthoe falcata (L.f.) Ettingsh (Loranthaceae), an Indian Ayurvedic plant, on different arms of the immune system. HEDF was evaluated for immunological function by studying delayed type hypersensitivity (DTH) to sheep RBCs, nitric oxide (NO) release from murine peritoneal macrophages, phagocytic activity of polymorphonuclear (PMN) cells in vitro and reticuloendothelial system in vivo, plaque forming cell response of splenic lymphocytes to sheep erythrocytes, haemagglutination antibody titer and neutrophil adhesion test. Significant increase in NO production by mouse peritoneal macrophages was detected in culture supernatants indicated increased phagocytic activity of macrophages. After post oral administration of HEDF in three doses of 250, 475 and 950 mg/kg body weight, a significant increase in phagocytic activity of PMN cells/reticuloendothelial system, stimulation of neutrophil function and splenic antibody secreting cells, were also noticed. Stimulation of humoral immune response was further observed with elevation in haemagglutination antibody titer. Heightened DTH reaction suggested convincing evidence for activation of cellular immune system. Present study thus confirms the immunomodulatory activity of the hydroalcoholic extract of D. falcata and the immunomodulatory responses were found to be dose dependent manner.Keywords: Dendrophthoe falcata; Antibody titer; Neutrophil adhesion; Phagocytic activity.© 2011 JSR Publications. ISSN: 2070-0237 (Print); 2070-0245 (Online). All rights reserved.doi:10.3329/jsr.v3i3.7655               J. Sci. Res. 3 (3), 629-640 (2011)

Effect of a Mixture of Lactobacillus casei and Lactobacillus acidophilus Administered Orally on the Immune System in Mice

1986 ◽  
Vol 49 (12) ◽  
pp. 986-989 ◽  
Author(s):  
GABRIELA PERDIGON ◽  
MARIA ELENA NADER de MACIAS ◽  
SUSANA ALVAREZ ◽  
MARTA MEDICI ◽  
GUILLERMO OLIVER ◽  
...  
Keyword(s):  
Immune System ◽  
Lactobacillus Acidophilus ◽  
Lactobacillus Casei ◽  
Lymphocyte Activation ◽  
Fermented Milk ◽  
Peritoneal Macrophages ◽  
Oral Route ◽  
Carbon Clearance ◽  
Stimulation Of

The effects of an orally-administered mixture of Lactobacillus casei and Lactobacillus acidophilus on the immune system in Swiss albino mice were studied. Non-fermented milk containing viable cultures of both microorganisms was fed for different consecutive days to the animals, the effect of such feeding on their immune system was evinced by macrophage and lymphocyte activation. An increase both in the in vitro phagocytic activity of peritoneal macrophages and in the carbon clearance activity was observed. As regard the lymphocytic activity, the mixture produced a higher activation than that in the control mice. The enhanced macrophage and lymphocytic activity by administering cultures via the oral route, suggest the advisability of using the mixture of bacteria for a more efficient stimulation of the host immune response.

scholarly journals Granulocyte-macrophage colony-stimulating factor enhances selective effector functions of tissue-derived macrophages

Blood ◽  
1988 ◽  
Vol 72 (2) ◽  
pp. 573-578
Author(s):  
DL Coleman ◽  
JA Chodakewitz ◽  
AH Bartiss ◽  
JW Mellors
Keyword(s):  
Peritoneal Macrophages ◽  
Colony Stimulating Factor ◽  
Murine Peritoneal Macrophage ◽  
Effector Functions ◽  
Gm Csf ◽  
Macrophage Colony Stimulating Factor ◽  
Macrophage Colony ◽  
Stimulating Factor ◽  
Stimulation Of

Granulocyte-macrophage colony-stimulating factor (GM-CSF) is produced by a variety of cells at sites of exposure to antigens. GM-CSF has a stimulatory effect on a number of neutrophil functions, but the effect on macrophage function is less clear. We investigated the effect of purified murine recombinant GM-CSF on murine peritoneal macrophage oxidative metabolism, Fc-dependent phagocytosis, anti-Toxoplasma activity, and expression of class II major histocompatibility antigen (Iad). GM-CSF significantly increased phorbol myristate acetate- and zymosan-elicited H2O2 release by resident and thioglycollate-elicited macrophages after 48 hours in vitro. The effect of recombinant GM-CSF was blocked by polyclonal anti-GM-CSF antibody and was not altered by lipopolysaccharide (0.01 to 1.0 microgram/mL). GM-CSF also stimulated Fc-dependent phagocytosis by peritoneal macrophages, although the stimulation of resident macrophages (1.4-fold) was less dramatic than that of thioglycollate-elicited cells (2.1-fold). GM-CSF (at doses up to 100 U/mL) had no effect on macrophage anti-Toxoplasma activity or on expression of Iad. In addition to stimulating macrophage growth, GM-CSF selectively promotes the functional capacity of tissue-derived macrophages.

scholarly journals Granulocyte-macrophage colony-stimulating factor enhances selective effector functions of tissue-derived macrophages

Blood ◽  
1988 ◽  
Vol 72 (2) ◽  
pp. 573-578 ◽  
Author(s):  
DL Coleman ◽  
JA Chodakewitz ◽  
AH Bartiss ◽  
JW Mellors
Keyword(s):  
Peritoneal Macrophages ◽  
Colony Stimulating Factor ◽  
Murine Peritoneal Macrophage ◽  
Effector Functions ◽  
Gm Csf ◽  
Macrophage Colony Stimulating Factor ◽  
Macrophage Colony ◽  
Stimulating Factor ◽  
Stimulation Of

Abstract Granulocyte-macrophage colony-stimulating factor (GM-CSF) is produced by a variety of cells at sites of exposure to antigens. GM-CSF has a stimulatory effect on a number of neutrophil functions, but the effect on macrophage function is less clear. We investigated the effect of purified murine recombinant GM-CSF on murine peritoneal macrophage oxidative metabolism, Fc-dependent phagocytosis, anti-Toxoplasma activity, and expression of class II major histocompatibility antigen (Iad). GM-CSF significantly increased phorbol myristate acetate- and zymosan-elicited H2O2 release by resident and thioglycollate-elicited macrophages after 48 hours in vitro. The effect of recombinant GM-CSF was blocked by polyclonal anti-GM-CSF antibody and was not altered by lipopolysaccharide (0.01 to 1.0 microgram/mL). GM-CSF also stimulated Fc-dependent phagocytosis by peritoneal macrophages, although the stimulation of resident macrophages (1.4-fold) was less dramatic than that of thioglycollate-elicited cells (2.1-fold). GM-CSF (at doses up to 100 U/mL) had no effect on macrophage anti-Toxoplasma activity or on expression of Iad. In addition to stimulating macrophage growth, GM-CSF selectively promotes the functional capacity of tissue-derived macrophages.

scholarly journals Differential stimulation of murine lymphoma growth in vitro by normal and BCG-activated macrophages.

1975 ◽  
Vol 142 (4) ◽  
pp. 887-902 ◽  
Author(s):  
C F Nathan ◽  
W D Terry
Keyword(s):  
Tumor Cell ◽  
Peritoneal Macrophages ◽  
Similar Degree ◽  
Thymidine Uptake ◽  
Tumor Cell Growth ◽  
Bacille Calmette Guerin ◽  
Fibroblast Line ◽  
Murine Fibroblast ◽  
Stimulation Of

Peritoneal macrophages from mice infected with Bacille Calmette-Guérin (BCG) and from normal mice were examined for their effects in vitro on thymidine uptake by 10 murine lymphomas, a murine fibroblast line, and a guinea pig hepatoma. Only the murine fibroblast line showed growth inhibition in the presence of BCG macrophages. For the majority of tumors, normal macrophages were profoundly stimulatory to tumor cell DNA synthesis, while BCG macrophages were much less stimulatory, without being frankly inhibitory. The effect of 2-mercaptoethanol on tumor cell growth was also studied. All lymphomas stimulated to grow more rapidly in vitro by normal macrophages were stimulated to a similar degree by 2-mercaptoethanol.

scholarly journals A quantitative study of pinocytosis and intracellular proteolysis in rat peritoneal macrophages

1977 ◽  
Vol 168 (3) ◽  
pp. 365-372 ◽  
Author(s):  
M K Pratten ◽  
K E Williams ◽  
J B Lloyd
Keyword(s):  
Plasma Membrane ◽  
Binding Sites ◽  
Culture Medium ◽  
Peritoneal Macrophages ◽  
The Other ◽  
High Rate ◽  
Intracellular Proteolysis ◽  
Pinocytic Vesicles ◽  
Stimulation Of

A method for the culture of rat peritoneal macrophages in vitro is described, in which pinocytic uptake of colloidal [198 Au]gold, 125I--labelled poly(vinylpyrrolidone) and [14C]sucrose proceeds at contant and fairly reproducible rates for several hours. The rat of uptake of colloidal [198 Au]gold, which wxhibited some inter-batch variation, was approx. 100 times that of the other two substrates. Colloidal gold did not affect the rate of uptake of 125I-labelled poly(vinylpyrrolidone) and therefore its own high rate of uptake could not be attributed to a stimulation of the formation of pinocytic vesicles. It conclude that uptake of collodial gold is highly dependent on adsorption on binding sites on the plasma membrane. Uptake of formaldehyde-treated 125I-labelled bovine serum albumin was followed by the release of [125I]iodo-L-tyrosine into the culture medium and took place at a rate intermediate between those of collodial [198Au]gold and the other two non-digestible substrates, 125I-labelled poly(vinylpyrrolidone) and [14C]sucrose.

Lipophilic derivative of muramyl dipeptide is more active than muramyl dipeptide in priming macrophages to release superoxide anion

1980 ◽  
Vol 29 (2) ◽  
pp. 617-622 ◽  
Author(s):  
M J Pabst ◽  
N P Cummings ◽  
T Shiba ◽  
S Kusumoto ◽  
S Kotani
Keyword(s):  
Superoxide Anion ◽  
Alternative Pathway ◽  
Muramyl Dipeptide ◽  
Peritoneal Macrophages ◽  
Systemic Effect ◽  
Parent Molecule ◽  
Lipophilic Derivative ◽  
Stimulation Of

Mouse peritoneal macrophages, when treated with a lipophilic derivative of muramyl dipeptide either in vitro or in vivo by intraperitoneal injection, showed a more than fivefold increase in their ability to generate superoxide anion after stimulation of the macrophages with phorbol myristate acetate. This response was more than twice that observed with the parent molecule, muramyl dipeptide (MDP). Unlike MDP, which has a systemic effect, the lipophilic derivative, [B30]-MDP, did not alter the response of peritoneal macrophages when given subcutaneously in the flank, suggesting that [B30]-MDP remains localized at the site of injection. The enhanced effect of [B30]-MDP over MDP appeared to be due to the inherent lipophilicity of the molecule, and was probably not due to either stimulation of T lymphocytes or activation of the alternative pathway of complement.

Exercise-induced stimulation of murine macrophage phagocytosis may be mediated by thyroxine

1996 ◽  
Vol 80 (3) ◽  
pp. 899-903 ◽  
Author(s):  
M. A. Forner ◽  
C. Barriga ◽  
E. Ortega
Keyword(s):  
Plasma Concentrations ◽  
Peritoneal Macrophages ◽  
Phagocytic Function ◽  
Physiological Concentration ◽  
Phagocytic Capacity ◽  
Macrophage Phagocytosis ◽  
Exercise Induced ◽  
Previous Training ◽  
Stimulation Of

The present study was designed to test the hypothesis that changes in plasma concentrations of hormones may be responsible for the exercise-induced macrophage phagocytic stimulation. The effect of 30-min incubation of macrophages with plasma from mice previously exposed to swimming until exhaustion (with or without previous training) was studied, and the results showed a similar stimulation of the phagocytic capacity (attachment and ingestion) of these cells to that found in previous studies after exercise. Also, changes in plasma concentration of both thyroxine (T4) and 3,3′,5-triiodo-L-thyronine (T3) after exercise were measured, and their effect on phagocytic capacity after in vitro incubation with peritoneal macrophages was investigated. Results indicated that, after exercise, plasma concentrations of T3 and T4 increased. Incubation of peritoneal macrophages for 30 min with a concentration of T3 similar to that observed in the plasma immediately after exercise (1.5 ng/ml) induced no modifications in the phagocytic capacity. However, a physiological concentration of T4 after exercise (75 ng/ml) stimulated the phagocytic capacity of peritoneal macrophages. In addition, a 10,000-fold greater concentration of these thyroid hormones did not modify the macrophage function. It is concluded that physiological concentration of T4 may be a mediator of the stimulation of the phagocytic function in macrophages induced by exercise.

Sign in / Sign up

Export Citation Format

Share Document