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1.
PLoS One ; 17(1): e0263256, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-35100296

RESUMEN

Metamorphosis in the insect larva is associated with disintegration, engulf and digestion of larval tissues. These processes are accompanied by a significant shift in physiological parameters like high activity of hydrolytic enzymes and decrease of pH. In the way, the metamorphosing larva resembles the processes occurring in the wound at the stage of inflammation. Based on this thesis, we put forward the idea of the possibility of using insect phagocytes in the wound treatment. The search for a suitable insect cell line and the study of its properties were the purpose of the work. The abilities of insect phagocytes to retain viability and functional activity under conditions physiological for humans were also investigated. We found that blue blowfly Calliphora vicina larvae had histolysocytes, a specialized population of professional phagocytes involved in the histolysis. In vitro, histolysocytes possess high phagocytic activity to fragments of vertebrate soft tissues and debris. These cells retain viability and functional activity for a long time under conditions that are physiological for vertebrate cells. Moreover histolysocytes can realize the humoral control over the bacteria through the synthesis of antimicrobial peptides. So histolysocytes have the potential to be used as xenogeneic phagocytes in the wound treatment. The data obtained allow proceeding to experiments on laboratory animals for studying the effect of such therapy on the wound healing process.


Asunto(s)
Fagocitos/fisiología , Cicatrización de Heridas , Animales , Antiinfecciosos/farmacología , Diferenciación Celular/efectos de los fármacos , Pollos , Dípteros , Hemocitos/efectos de los fármacos , Hemocitos/fisiología , Cuerpos de Inclusión/efectos de los fármacos , Cuerpos de Inclusión/ultraestructura , Modelos Biológicos , Fagocitos/ultraestructura , Fagocitosis/efectos de los fármacos , Pupa/efectos de los fármacos , Pupa/fisiología , Porcinos , Cicatrización de Heridas/efectos de los fármacos
2.
PLoS One ; 12(3): e0173559, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28278280

RESUMEN

Biofilms, sedimented microbial communities embedded in a biopolymer matrix cause vast majority of human bacterial infections and many severe complications such as chronic inflammatory diseases and cancer. Biofilms' resistance to the host immunity and antibiotics makes this kind of infection particularly intractable. Antimicrobial peptides (AMPs) are a ubiquitous facet of innate immunity in animals. However, AMPs activity was studied mainly on planktonic bacteria and little is known about their effects on biofilms. We studied structure and anti-biofilm activity of AMP complex produced by the maggots of blowfly Calliphora vicina living in environments extremely contaminated by biofilm-forming germs. The complex exhibits strong cell killing and matrix destroying activity against human pathogenic antibiotic resistant Escherichia coli, Staphylococcus aureus and Acinetobacter baumannii biofilms as well as non-toxicity to human immune cells. The complex was found to contain AMPs from defensin, cecropin, diptericin and proline-rich peptide families simultaneously expressed in response to bacterial infection and encoded by hundreds mRNA isoforms. All the families combine cell killing and matrix destruction mechanisms, but the ratio of these effects and antibacterial activity spectrum are specific to each family. These molecules dramatically extend the list of known anti-biofilm AMPs. However, pharmacological development of the complex as a whole can provide significant advantages compared with a conventional one-component approach. In particular, a similar level of activity against biofilm and planktonic bacteria (MBEC/MIC ratio) provides the complex advantage over conventional antibiotics. Available methods of the complex in situ and in vitro biosynthesis make this idea practicable.


Asunto(s)
Antibacterianos/farmacología , Péptidos Catiónicos Antimicrobianos/farmacología , Bacterias/efectos de los fármacos , Biopelículas/efectos de los fármacos , Dípteros/fisiología , Farmacorresistencia Bacteriana/efectos de los fármacos , Larva/fisiología , Animales , Biopelículas/crecimiento & desarrollo , Productos Biológicos , Pruebas de Sensibilidad Microbiana
3.
In Vitro Cell Dev Biol Anim ; 53(1): 33-42, 2017 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-27586266

RESUMEN

Antimicrobial peptides accumulated in the hemolymph in response to infection are a key element of insect innate immunity. The involvement of the fat body and hemocytes in the antimicrobial peptide synthesis is widely acknowledged, although release of the peptides present in the hemolymph from the immune cells was not directly verified so far. Here, we studied the presence of antimicrobial peptides in the culture medium of fat body cells and hemocytes isolated from the blue blowfly Calliphora vicina using complex of liquid chromatography, mass spectrometry, and antimicrobial activity assays. Both fat body and hemocytes are shown to synthesize and release to culture medium defensin, cecropin, diptericins, and proline-rich peptides. The spectra of peptide antibiotics released by the fat body and hemocytes partially overlap. Thus, the results suggest that insect fat body and blood cells are capable of releasing mature antimicrobial peptides to the hemolymph. It is notable that the data obtained demonstrate dramatic difference in the functioning of insect antimicrobial peptides and their mammalian counterparts localized into blood cells' phagosomes where they exert their antibacterial activity.


Asunto(s)
Péptidos Catiónicos Antimicrobianos/biosíntesis , Péptidos Catiónicos Antimicrobianos/farmacología , Dípteros/citología , Cuerpo Adiposo/citología , Hemocitos/citología , Secuencia de Aminoácidos , Animales , Péptidos Catiónicos Antimicrobianos/química , Células Cultivadas , Fraccionamiento Químico , Cromatografía Líquida de Alta Presión , Medios de Cultivo/farmacología , Larva/citología , Larva/efectos de los fármacos , Linfocitos/citología , Linfocitos/efectos de los fármacos , Peso Molecular
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