Functionalized Surface-Charged SiO2 Nanoparticles Induce Pro-Inflammatory Responses, but Are Not Lethal to Caco-2 Cells

2020 ◽  
Vol 33 (5) ◽  
pp. 1226-1236 ◽  
Author(s):  
Saeko Tada-Oikawa ◽  
Mana Eguchi ◽  
Michiko Yasuda ◽  
Kiyora Izuoka ◽  
Akihiko Ikegami ◽  
...  
Keyword(s):  
Inflammatory Responses ◽  
Sio2 Nanoparticles ◽  
Functionalized Surface

scholarly journals A CYTOLOGICAL STUDY OF IMPRINT SMEARS (TOUCH PREPARATION CYTOLOGY) TO EVALUATE THE TOXICITY OF METAL-CONTAINING NANOPARTICLES IN EXPERIMENTAL ANIMALS

2020 ◽  
Vol 99 (1) ◽  
pp. 120-124
Author(s):  
R. R. Sakhautdinova ◽  
M. P. Sutunkova ◽  
I. A. Minigalieva ◽  
Tatyana V. Bushueva
Keyword(s):  
Inflammatory Responses ◽  
Cytological Study ◽  
Intraperitoneal Administration ◽  
Sio2 Nanoparticles ◽  
Mesenteric Lymph Nodes ◽  
Nickel Oxide Nanoparticles ◽  
Experimental Animals ◽  
Touch Preparation ◽  
Student’S T ◽  
Tissue Specimens

Introduction. Touch preparation cytology is a well-known technique widely used in clinical practice. It can be also applied for an express assessment of cyto-morphological effects of metal-containing nanoparticles in experimental animals. Material and methods. We’ve studied 144 imprint smears (of the liver, kidneys, lungs, tracheobronchial and mesenteric lymph nodes) taken from 52 rats, weighed 280-300 g, aged 3.5 months. This was done following a subchronic intraperitoneal administration of TiO2, Al2O3, and SiO2 nanoparticles, in a range of doses, and a subacute (5-times) inhalational exposure to 1 mg/m3 NiO NPs. Leishman stain was used. Cytological markers were studied at х100/х1000 magnification, using a Carl Zeiss Primo Star microscope, with a USCMOS camera for visualization. The count was done for every 200 cells of lung, liver and kidney specimens and for every 100 cells of lymph node tissue. The differences between the group means (in case of quantitative results) were analyzed using a Student’s t-test. The differences between the group means were considered statistically significant if the probability of those differences being accidental didn’t exceed 5% (р < 0,05). Results. We report the principal results obtained in a cytological study of imprint smears (touch preparations) of rat organs following the exposure to metal-containing nanoparticles. The main types of cellular responses were determined. Degenerative and dystrophic changes were observed in touch preparations of the liver, kidneys, and lungs following administration of nanoparticles in a range of doses and by various routes of exposure. Hyperergic inflammatory responses were seen upon the exposure to nickel oxide nanoparticles. A local cellular immune response was observed as an increase of macrophage percentage in imprint smears of some organs. Conclusion. The use of touch preparation cytology together with histological examination of tissue specimens expand opportunities for a more relevant morphological and quantitative analysis when studying the toxic effects of metal-containing nanoparticles.

Anti-β2 Glycoprotein I Antibodies Cause Inflammation and Recruit Dendritic Cells in Platelet Clearance

2001 ◽  
Vol 86 (11) ◽  
pp. 1257-1263 ◽  
Author(s):  
Attilio Bondanza ◽  
Angelo Manfredi ◽  
Valérie Zimmermann ◽  
Matteo Iannacone ◽  
Angela Tincani ◽  
...  
Keyword(s):  
Dendritic Cells ◽  
Inflammatory Responses ◽  
Glycoprotein I ◽  
Activated Platelets ◽  
Tnf Α ◽  
Per Se ◽  
Antigen Presenting ◽  
Antiinflammatory Cytokine

SummaryScavenger phagocytes are mostly responsible for the in vivo clearance of activated or senescent platelets. In contrast to other particulate substrates, the phagocytosis of platelets does not incite pro-inflammatory responses in vivo. This study assessed the contribution of macrophages and dendritic cells (DCs) to the clearance of activated platelets. Furthermore, we verified whether antibodies against the β2 Glycoprotein I (β2GPI), which bind to activated platelets, influence the phenomenon. DCs did not per se internalise activated platelets. In contrast, macrophages efficiently phagocytosed platelets. In agreement with the uneventful nature of the clearance of platelets in vivo, phagocytosing macrophages did not release IL-1β, TNF-α or IL-10. β2GPI bound to activated platelets and was required for their recognition by anti-ββ2GPI antibodies. DCs internalised platelets opsonised by anti-ββ2GPI antibodies. The phagocytosis of opsonised platelets determined the release of TNF-α and IL-1β by DCs and macrophages. Phagocytosing macrophages, but not DCs, secreted the antiinflammatory cytokine IL-1β0. We conclude that anti-ββ2GPI antibodies cause inflammation during platelet clearance and shuttle platelet antigens to antigen presenting DCs.

Oxidative Stress and Atherosclerosis: Its Relationship to Growth Factors, Thrombus Formation and Therapeutic Approaches

1999 ◽  
Vol 82 (S 01) ◽  
pp. 32-37 ◽  
Author(s):  
Karlheinz Peter ◽  
Wolfgang Kübler ◽  
Johannes Ruef ◽  
Thomas K. Nordt ◽  
Marschall S. Runge ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Growth Factors ◽  
Vessel Wall ◽  
Inflammatory Responses ◽  
Plaque Rupture ◽  
Thrombus Formation ◽  
Vascular Lesion ◽  
Coagulation System ◽  
Therapeutic Approaches ◽  
Causative Relationship

SummaryThe initiating event of atherogenesis is thought to be an injury to the vessel wall resulting in endothelial dysfunction. This is followed by key features of atherosclerotic plaque formation such as inflammatory responses, cell proliferation and remodeling of the vasculature, finally leading to vascular lesion formation, plaque rupture, thrombosis and tissue infarction. A causative relationship exists between these events and oxidative stress in the vessel wall. Besides leukocytes, vascular cells are a potent source of oxygen-derived free radicals. Oxidants exert mitogenic effects that are partially mediated through generation of growth factors. Mitogens, on the other hand, are potent stimulators of oxidant generation, indicating a putative self-perpetuating mechanism of atherogenesis. Oxidants influence the balance of the coagulation system towards platelet aggregation and thrombus formation. Therapeutic approaches by means of antioxidants are promising in both experimental and clinical designs. However, additional clinical trials are necessary to assess the role of antioxidants in cardiovascular disease.

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