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1.
Biol. Res ; 51: 12, 2018. graf
Article in English | LILACS | ID: biblio-950898

ABSTRACT

BACKGROUND: Chemokine (C-C motif) receptor 6 (CCR6) is present in sperm and plays a significant role in sperm motility and chemotaxis acting in the reproductive tracts. However, the expression and functional significance of CCR6 in testis are still poorly understood, especially in the process of spermatogenesis. METHODS AND RESULTS: CCR6 was expressed in spermatogenic cell lines and its expression was shown in an age-dependent upregulation manner from puberty to adulthood in mouse testis. Immunostaining results confirmed the localization of CCR 6 in testis. Further chemotaxis assays demonstrated that spermatogenic cells GC-1 and -2 exhibited a directional movement toward CCR6-specific ligand such as CCL20 or Sertoli cells in vitro. CONCLUSIONS: The present findings indicate that CCR6 is involved in the chemotaxis of spermatogenic cells in vitro and promotes chemotaxis under non-inflammatory conditions during normal spermatogenesis.


Subject(s)
Humans , Animals , Male , Mice , Rabbits , Spermatogenesis/physiology , Chemotaxis/physiology , Cryptorchidism/metabolism , Chemokine CCL20/metabolism , Receptors, CCR6/metabolism , Sertoli Cells , Sperm Motility/physiology , Testis/physiology , Immunohistochemistry , Blotting, Western , Fluorescent Antibody Technique , Mice, Inbred C57BL
2.
Dental press j. orthod. (Impr.) ; 20(2): 16-19, Mar-Apr/2015. graf
Article in English | LILACS | ID: lil-745862

ABSTRACT

Deciduous teeth exfoliate as a result of apoptosis induced by cementoblasts, a process that reveals the mineralized portion of the root while attracting clasts. Root resorption in deciduous teeth is slow due to lack of mediators necessary to speed it up; however, it accelerates and spreads in one single direction whenever a permanent tooth pericoronal follicle, rich in epithelial growth factor (EGF), or other bone resorption mediators come near. The latter are responsible for bone resorption during eruption, and deciduous teeth root resorption and exfoliation. Should deciduous teeth be subjected to orthodontic movement or anchorage, mediators local levels will increase. Thus, one should be fully aware that root resorption in deciduous teeth will speed up and exfoliation will early occur. Treatment planning involving deciduous teeth orthodontic movement and/or anchorage should consider: Are clinical benefits relevant enough as to be worth the risk of undergoing early inconvenient root resorption?.


O dente decíduo é esfoliado graças à apoptose em seus cementoblastos, que desnuda a parte mineralizada da raiz e atrai os clastos. A rizólise é lenta, pois faltam mediadores em quantidade para acelerar o processo, mas ela se acelera e unidireciona quando se aproxima um folículo pericoronário de dente permanente rico em EGF e outros mediadores da reabsorção óssea - os responsáveis pelas reabsorções óssea na erupção e dentária decídua na rizólise e esfoliação. Se houver movimentação ortodôntica ou ancoragem em dentes decíduos, aumenta-se, também, o nível local desses mesmos mediadores, devendo-se estar bem consciente de que haverá uma aceleração da rizólise e, em decorrência, uma antecipação de sua esfoliação. No planejamento de casos em que dentes decíduos estejam envolvidos na movimentação ortodôntica e/ou ancoragem, deve-se ponderar: o benefício clínico para o paciente será relevante, a ponto de valer o risco de uma rizólise abreviada e inconveniente?.


Subject(s)
Humans , Tooth, Deciduous/physiology , Tooth Movement Techniques/methods , Root Resorption/physiopathology , Tooth Eruption/physiology , Tooth Exfoliation/physiopathology , Bone Resorption/physiopathology , Chemotaxis/physiology , Apoptosis/physiology , Intercellular Signaling Peptides and Proteins/physiology , Dental Cementum/physiology , Dental Sac/cytology , Dental Sac/physiology , Epidermal Growth Factor/physiology , Epithelial Cells/physiology , Orthodontic Anchorage Procedures/methods , Odontoblasts/physiology
3.
Braz. j. med. biol. res ; 48(2): 161-166, 02/2015. tab, graf
Article in English | LILACS | ID: lil-735848

ABSTRACT

Our aim was to investigate the role of chemokines in promoting instability of coronary atherosclerotic plaques and the underlying molecular mechanism. Coronary angiography and intravascular ultrasound (IVUS) were performed in 60 stable angina pectoris (SAP) patients and 60 unstable angina pectoris (UAP) patients. The chemotactic activity of monocytes in the 2 groups of patients was examined in Transwell chambers. High-sensitivity C-reactive protein (hs-CRP), monocyte chemoattractant protein-1 (MCP-1), regulated on activation in normal T-cell expressed and secreted (RANTES), and fractalkine in serum were examined with ELISA kits, and expression of MCP-1, RANTES, and fractalkine mRNA was examined with real-time PCR. In the SAP group, 92 plaques were detected with IVUS. In the UAP group, 96 plaques were detected with IVUS. The plaques in the UAP group were mainly lipid 51.04% (49/96) and the plaques in the SAP group were mainly fibrous 52.17% (48/92). Compared with the SAP group, the plaque burden and vascular remodeling index in the UAP group were significantly greater than in the SAP group (P<0.01). Chemotactic activity and the number of mobile monocytes in the UAP group were significantly greater than in the SAP group (P<0.01). Concentrations of hs-CRP, MCP-1, RANTES, and fractalkine in the serum of the UAP group were significantly higher than in the serum of the SAP group (P<0.05 or P<0.01), and expression of MCP-1, RANTES, and fractalkine mRNA was significantly higher than in the SAP group (P<0.05). MCP-1, RANTES, and fractalkine probably promote instability of coronary atherosclerotic plaque.


Subject(s)
Adult , Female , Humans , Male , Middle Aged , Angina Pectoris/metabolism , Chemokines/metabolism , Chemotaxis/physiology , Coronary Artery Disease/metabolism , Monocytes/metabolism , Plaque, Atherosclerotic/physiopathology , Angina Pectoris/physiopathology , C-Reactive Protein/analysis , /blood , /blood , /blood , Coronary Artery Disease/physiopathology , Real-Time Polymerase Chain Reaction , Ultrasonography, Interventional
4.
Biol. Res ; 47: 1-9, 2014. ilus, tab
Article in English | LILACS | ID: biblio-950754

ABSTRACT

Diabetic retinopathy is one of the most important causes of blindness. The underlying mechanisms of this disease include inflammatory changes and remodeling processes of the extracellular-matrix (ECM) leading to pericyte and vascular endothelial cell damage that affects the retinal circulation. In turn, this causes hypoxia leading to release of vascular endothelial growth factor (VEGF) to induce the angiogenesis process. Alpha-1 antitrypsin (AAT) is the most important circulating inhibitor of serine proteases (SERPIN). Its targets include elastase, plasmin, thrombin, trypsin, chymotrypsin, proteinase 3 (PR-3) and plasminogen activator (PAI). AAT modulates the effect of protease-activated receptors (PARs) during inflammatory responses. Plasma levels of AAT can increase 4-fold during acute inflammation then is so-called acute phase protein (APPs). Individuals with low serum levels of AAT could develop disease in lung, liver and pancreas. AAT is involved in extracellular matrix remodeling and inflammation, particularly migration and chemotaxis of neutrophils. It can also suppress nitric oxide (NO) by nitric oxide sintase (NOS) inhibition. AAT binds their targets in an irreversible way resulting in product degradation. The aim of this review is to focus on the points of contact between multiple factors involved in diabetic retinopathy and AAT resembling pleiotropic effects that might be beneficial.


Subject(s)
Humans , Animals , Serine Proteinase Inhibitors/therapeutic use , alpha 1-Antitrypsin/therapeutic use , Diabetic Retinopathy/drug therapy , Cell Hypoxia , Serine Proteinase Inhibitors/metabolism , Cell Movement/physiology , Chemotaxis/physiology , alpha 1-Antitrypsin/metabolism , NF-kappa B/metabolism , Tumor Necrosis Factor-alpha/metabolism , Inflammation Mediators/antagonists & inhibitors , Nitric Oxide Synthase/antagonists & inhibitors , Protective Agents/metabolism , Receptors, Proteinase-Activated/metabolism , Diabetic Retinopathy/physiopathology , Free Radicals , Inflammation/metabolism , Anti-Inflammatory Agents/metabolism , Anti-Inflammatory Agents/therapeutic use , Neutrophils/physiology
6.
Mem. Inst. Oswaldo Cruz ; 106(4): 461-466, June 2011. ilus, graf, tab
Article in English | LILACS | ID: lil-592190

ABSTRACT

Chagas disease is a major public health issue and is mainly spread by Triatominae insects (Hemiptera: Reduviidae). Rhodnius prolixus is the main vector species in Northern South America. Host-seeking behaviour in R. prolixus is mediated by different compounds that are produced by and emanate from the host or microbiota on the host's skin. We tested the behavioural responses of sylvatic first filial generation (F1) and colony insects to extracts of human skin with a dual choice olfactometer. In addition, we compared the antennal phenotypes in both populations. No statistical differences were found between the two populations at the behavioural level. Both showed a preference for face and feet extracts and this effect was abolished for face extracts after treatment with an antibacterial gel. The observation of the antennal phenotype showed that there were differences between both groups in the total length, total surface area and number and density of bristles. However, the number and density of chemoreceptive sensilla (basiconic and thin and thick-walled trichoids) and the total density of sensilla did not show statistically significant differences. These results demonstrate that colony insects, which have only been fed with living hens for the last 30 years, are attracted by human skin extracts in a similar way as F1 sylvatic insects.


Subject(s)
Animals , Female , Humans , Male , Arthropod Antennae/physiology , Behavior, Animal/physiology , Insect Vectors/physiology , Pheromones , Rhodnius/physiology , Skin , Animals, Laboratory , Arthropod Antennae , Arthropod Antennae/ultrastructure , Chemoreceptor Cells/physiology , Chemotaxis/physiology , Face , Foot , Phenotype , Rhodnius , Tissue Extracts
7.
Genet. mol. res. (Online) ; 3(1): 92-101, Mar. 2004.
Article in English | LILACS | ID: lil-417581

ABSTRACT

The availability of the complete genome of the Gram-negative beta-proteobacterium Chromobacterium violaceum has increasingly impacted our understanding of this microorganism. This review focuses on the genomic organization and structural analysis of the deduced proteins of the chemosensory adaptation system of C. violaceum. C. violaceum has multiple homologues of most chemotaxis genes, organized mostly in clusters in the bacterial genome. We found at least 67 genes, distributed in 10 gene clusters, involved in the chemotaxis of C. violaceum. A close examination of the chemoreceptors methyl-accepting chemotaxis proteins (MCPs), and the deduced sequences of the members of the two-component signaling system revealed canonical motifs, described as essential for the function of the deduced proteins. The chemoreceptors found in C. violaceum include the complete repertoire of such genes described in bacteria, designated as tsr, tar, trg, and tap; 41 MCP loci were found in the C. violaceum genome. Also, the C. violaceum genome includes a large repertoire of the proteins of the chemosensory transducer system. Multiple homologues of bacterial chemotaxis genes, including CheA, CheB, CheD, CheR, CheV, CheY, CheZ, and CheW, were found in the C. violaceum genome


Subject(s)
Chromobacterium/genetics , Flagella/genetics , Genes, Bacterial/genetics , Bacterial Proteins/genetics , Chemotaxis/genetics , Chromobacterium/physiology , Flagella/physiology , Genome, Bacterial , Genes, Bacterial/physiology , Bacterial Proteins/physiology , Membrane Proteins/genetics , Membrane Proteins/physiology , Chemotaxis/physiology
8.
J Biosci ; 2001 Jun; 26(2): 157-66
Article in English | IMSEAR | ID: sea-110788

ABSTRACT

A drop assay for chemotaxis to cAMP confirms that both anterior-like cells (ALC) and prestalk cells (pst cells) respond to cAMP gradients. We present evidence that the chemotactic response of both ALC and pst cells is suppressed by ammonia, but a higher concentration of ammonia is required to suppress the response in pst cells. ALC show a chemotactic response to cAMP when moving on a substratum of prespore cells in isolated slug posteriors incubated under oxygen. ALC chemotaxis on a prespore cell substratum is suppressed by the same concentration of ammonia that suppresses ALC chemotaxis on the agar substratum in drop assays. Chemotaxis suppression is mediated by the unprotonated (NH3) species of ammonia. The observed suppression, by ammonia, of ALC chemotaxis to cAMP supports our earlier hypothesis that ammonia is the tip-produced suppressor of such chemotaxis. We discuss implications of ammonia sensitivity of pst cells and ALC with regard to the movement and localization of ALC and pst cells in the slug and to the roles played by ALC in fruiting body formation. In addition, we suggest that a progressive decrease in sensitivity to ammonia is an important part of the maturation of ALC into pst cells.


Subject(s)
Ammonia/pharmacology , Animals , Buffers , Chemotaxis/physiology , Cyclic AMP/metabolism , Dictyostelium/cytology , Hydrogen-Ion Concentration , Morphogenesis/drug effects
9.
Rev. bras. biol ; 60(3): 405-414, ago. 2000. graf
Article in English | LILACS | ID: lil-280968

ABSTRACT

Recent studies have show that small marine herbivores with limited mobility (mesograzers) often feed on macroalgae chemically defended against fishes or sea-urchins. In order to verify the involved mechanisms of chemotaxis or chemical defense into this process in Brazilian littoral, two species of brown alga Dictyota menstrualis and Dictyota mertensii were studied against the limited mobility herbivores, the amphipod Parhyale hawaiensis and the crab Pachygrapsus transversus. These two species were studied in order to verify the action of their crude extracts in the defense and chemotaxis processes related to limited mobility of these herbivores. Feeding preference assays revealed that P. hawaiensis do not eaten these Dictyota species. P. transversus do not eaten D. menstrualis either, but consumed large amounts of D. mertensii. Chemical deterrence assays showed that extracts of these species act as feeding deterrent to both species of herbivores. In addition, chemotaxis assays demonstrated that both herbivores are significantly negative chemotactic probably due to the presence of complementary metabolites into artificial foods. Considering that both Dictyota species exhibit active extracts against these small herbivores, we suppose that the non-occurrence of these herbivore species in close relationship with the seaweeds D. menstrualis and D. mertensii may explain the defense action of both extracts related to these mesograzers


Subject(s)
Animals , Brachyura , Chemotactic Factors , Chemotaxis/physiology , Feeding Behavior/drug effects , Plant Extracts/pharmacology , Seaweed/chemistry , Analysis of Variance , Case-Control Studies , Defense Mechanisms
11.
Rev. Soc. Odontol. La Plata ; 12(22): 22-8, abr. 1999. tab
Article in Spanish | LILACS | ID: lil-243386

ABSTRACT

Para que se produzca regeneración periodontal, tanto las células progenitoras del ligamento periodontal como las óseas, deben migrar a la superficie radicular, unirse a ella, madurar y proliferar. La selección de un factor de crecimiento es fundamental para dicha regeneración. Estos factores de crecimiento (FGFs, PDGF, IFGs, TGFs, EFG, fibronectina), junto a ciertas proteínas de inserción, tienen un papel relevante en la cicatrización periodontal


Subject(s)
Wound Healing/physiology , Growth Substances/therapeutic use , Periodontal Diseases/therapy , Stem Cells/physiology , Chemotaxis/physiology , Epidermal Growth Factor/therapeutic use , Fibroblast Growth Factors/therapeutic use , Fibronectins/therapeutic use , Guided Tissue Regeneration , Periodontal Ligament/physiology , Platelet-Derived Growth Factor/therapeutic use , Bone Regeneration/physiology , Somatomedins/therapeutic use , Transforming Growth Factors/therapeutic use
13.
Arch. argent. alerg. inmunol. clín ; 28(2): 12-7, 1997. ilus
Article in Spanish | LILACS | ID: lil-207525

ABSTRACT

Durante la respuesta inmune existe una colaboración mutua entre linfocitos y fagocitos que sufren un proceso de activación a través de la liberación de mediadores solubles polipeptídicos que se denominan citokinas. Son de bajo peso molecular


Subject(s)
Humans , Cytokines/physiology , Hypersensitivity/physiopathology , Lymphokines/metabolism , Acute-Phase Reaction , Chemotaxis/physiology , Hypersensitivity/immunology , Inflammation/physiopathology
14.
Arch. med. res ; 27(3): 311-8, 1996. ilus, tab
Article in English | LILACS | ID: lil-200328

ABSTRACT

This quantitative ultrastructural survery of E. histolytica locomotion in Boyden chambers supports the concept that this parasitis is capable of random, chemokinetic and chemotactic motility. An E. histolytica committed to chemotaxis will flatten over the filter, accumulate smaller vacuoles at the front of the cell, and will also project pseudopods and its polarized body towards and alongside the chemoattractant axis, respectively. Other cell features such as cell polarization, membrane ruffling, hyaline, total number of pseudopods and caudal displacement of the nucleus appear to be associated with the locomotion efforts as such, perhaps reflecting speed (chemokinesis) but irrespective of orientation (chemotaxis). Finally, only on of the 11 features that were analyzed (i.e., number of vacuoles) failed to be distinctly associated with any of the movement forms studied. E. histolytica appears to possess the full repertoire of locomotion modalities observed in free moving eukaryots, and its motility translates into ultrastructural landmarks that could be useful indicators of subcellular events related to locomotion


Subject(s)
Cell Movement/physiology , Chemotaxis/physiology , Entamoeba histolytica/ultrastructure , Cytological Techniques/standards
15.
Alergia (Méx.) ; 42(1): 9-13, ene.-feb. 1995.
Article in Spanish | LILACS | ID: lil-147856

ABSTRACT

El propósito del trabajo fue determinar si el extracto de Staphylococcus aureus in vitro puede modificar la quimiocinesis e inducir la quimiotaxis de las células polimorfonucleares de la sangre periférica en donadores sanos. Se determinó la quimiocinesis y la quimiotaxis de los polimorfonucleares de la sangre periférica de 30 donadores sanos de uno y otro sexo con un límite de edad entre 18 y 40 años. Se les extrajeron 5 mL de sangre periférica separando los polimorfonucleares por el método de Boyum y se retaron con extracto de Staphylococcus aureus y C5a como quimiotácticos, y solución de Hank para medir quimiocinesis. Esta tuvo un promedio de 54.6ñ8.8 µm, la respuesta quimiotáctica a C5a fue 89ñ12.5 µm y con el extracto bacteriano fue 103ñ20.1 µm (p<0.001. Análisis estadístico: prueba de Wilcoxon. Se concluye que el extracto completo de Staphylococcus aureus estímula in vitro la quimiotaxis de polimorfonucleares de donadores sanos y que esta estimulación es comparable con lo quimioatrayentes conocidos como C5a


Subject(s)
Adult , Middle Aged , Humans , Cell Extracts/immunology , Cell Extracts/isolation & purification , Chemotaxis/physiology , In Vitro Techniques , Methods , Cell Count/methods , Staphylococcus aureus/pathogenicity
17.
Bol. micol ; 8(1/2): 85-9, jul.-dic. 1993. tab
Article in Spanish | LILACS | ID: lil-140503

ABSTRACT

Se ensayó la actividad enzimática de algunas Saprolegniales (Achlya americana, A. apiculata, A. oligacantha, A. polyandra, A. prolifera, Dictyuchus monosporus, Isoachlyatouroloides, Saprolegnia diclina y S. parasitica), en distintos medios sólidos. Estas especies fueron aisladas de materia orgánica flotante, en Río Santiago (Pdo. Ensenada, Provincia de Buenos Aires, Argentina), y se demostró que poseen actividad enzimática, in vitro, para la descomposición de pectina, celulosa, hemicelulosa, lignina y almidón


Subject(s)
Oomycetes/enzymology , Starch/metabolism , Cellulose/metabolism , Chemotaxis/physiology , Environmental Health , Lignin/metabolism , Oomycetes/isolation & purification , Pectins/metabolism , River Pollution
18.
Indian J Biochem Biophys ; 1989 Oct; 26(5): 343-7
Article in English | IMSEAR | ID: sea-26948

ABSTRACT

Activation profile of lysosomal enzymes in rat peritoneal macrophages elicited in response to three stimulants, thioglycollate (TG), protease peptone (PP) and lipopolysaccharide (LPS) was studied from 0 to 6 days. Macrophages elicited in response to LPS were larger in number and heterogeneous in nature while TG and PP induced cells were comparatively more homogeneous. Maximum elicitation of macrophages in response to the three stimulants, though at different degrees, was observed around 3 days. This could be correlated to increased blood monocytes. The progressive activation of macrophages reflected in corresponding decrease in total cellular protein content and increase in the activities of their lysosomal enzymes. The catalytic activities of aryl sulphatase, beta-glucuronidase and cathepsin D increased several fold (2-8 fold) over the resident values. TG elicited cells possessed the highest enzyme activities, followed by PP and LPS elicited ones. Beta-Glucuronidase was the most stimulated (4-8 fold) of the enzymes studied. The cellular catalytic activities of these enzymes were also enhanced 2- to 4-fold compared to the resident levels in the TG and PP elicited macrophages. Though the enzyme catalytic activities were increased in the LPS treated cells, their cellular levels remained below the resident activities in all the three enzymes studied. The results indicate that the events related to the elaboration of these macrophage lysosomal enzymes in vivo are subject to selective modulation and are stimulus specific.


Subject(s)
Animals , Caseins/pharmacology , Chemotaxis/physiology , Enzyme Activation , Lipopolysaccharides/pharmacology , Lysosomes/enzymology , Macrophages/enzymology , Male , Peptide Fragments/pharmacology , Rats , Rats, Inbred Strains , Thioglycolates/pharmacology
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