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1.
Cell Mol Life Sci ; 74(20): 3841-3850, 2017 10.
Artículo en Inglés | MEDLINE | ID: mdl-28612218

RESUMEN

When a constraint is removed, confluent cells migrate directionally into the available space. How the migration directionality and speed increase are initiated at the leading edge and propagate into neighboring cells are not well understood. Using a quantitative visualization technique-Particle Image Velocimetry (PIV)-we revealed that migration directionality and speed had strikingly different dynamics. Migration directionality increases as a wave propagating from the leading edge into the cell sheet, while the increase in cell migration speed is maintained only at the leading edge. The overall directionality steadily increases with time as cells migrate into the cell-free space, but migration speed remains largely the same. A particle-based compass (PBC) model suggests cellular interplay (which depends on cell-cell distance) and migration speed are sufficient to capture the dynamics of migration directionality revealed experimentally. Extracellular Ca2+ regulated both migration speed and directionality, but in a significantly different way, suggested by the correlation between directionality and speed only in some dynamic ranges. Our experimental and modeling results reveal distinct directionality and speed dynamics in collective migration, and these factors can be regulated by extracellular Ca2+ through cellular interplay. Quantitative visualization using PIV and our PBC model thus provide a powerful approach to dissect the mechanisms of collective cell migration.


Asunto(s)
Calcio/metabolismo , Comunicación Celular , Movimiento Celular , Epitelio Corneal/citología , Materiales Biocompatibles/química , Recuento de Células , Línea Celular , Dimetilpolisiloxanos/química , Epitelio Corneal/metabolismo , Humanos , Modelos Biológicos , Cicatrización de Heridas
2.
J Glaucoma ; 33(6): 400-408, 2024 Jun 01.
Artículo en Inglés | MEDLINE | ID: mdl-38506820

RESUMEN

PRCIS: In this cross-sectional analysis of UK Biobank participants, we find no adverse association between self-reported oral health conditions and either glaucoma or elevated intraocular pressures. PURPOSE: Poor oral health may cause inflammation, which accelerates the progression of neurodegenerative diseases. We investigated the relationship between oral health and glaucoma. PATIENTS: United Kingdom Biobank participants. METHODS: This is a cross-sectional analysis of participants categorized by self-reported oral health status. Multivariable linear and logistic regression models were used. Primary analysis examined the association with glaucoma prevalence. Secondary analyses examined associations with IOP, macular retinal nerve fiber layer (mRNFL), and ganglion cell inner plexiform layer (mGCIPL) thicknesses, and interaction terms with multitrait glaucoma polygenic risk scores (MTAG PRS) or intraocular pressure (IOP) PRS. RESULTS: A total of 170,815 participants (34.3%) reported current oral health problems, including painful or bleeding gums, toothache, loose teeth, and/or denture wear. A In all, 33,059, 33,004, 14,652, and 14,613 participants were available for analysis of glaucoma, IOP, mRNFL, and mGCIPL, respectively. No association between oral health and glaucoma was identified [odds ratio (OR): 1.04, 95% CI: 0.95-1.14]. IOPs were slightly lower among those with oral disease (-0.08 mm Hg, 95% CI: -0.15, -0.009); specifically, among those with loose teeth ( P =0.03) and denture-wearers ( P <0.0001). mRNFL measurements were lower among those with oral health conditions (-0.14 µm, 95% CI: -0.27, -0.0009), but mGCIPL measurements ( P =0.96) were not significantly different. A PRS for IOP or glaucoma did not modify relations between oral health and IOP or glaucoma ( P for interactions ≥​​​​0.17). CONCLUSIONS: Self-reported oral health was not associated with elevated IOP or an increased risk of glaucoma. Future studies should confirm the null association between clinically diagnosed oral health conditions and glaucoma.


Asunto(s)
Glaucoma , Presión Intraocular , Fibras Nerviosas , Salud Bucal , Células Ganglionares de la Retina , Humanos , Estudios Transversales , Reino Unido/epidemiología , Masculino , Femenino , Persona de Mediana Edad , Presión Intraocular/fisiología , Anciano , Fibras Nerviosas/patología , Glaucoma/epidemiología , Glaucoma/fisiopatología , Células Ganglionares de la Retina/patología , Autoinforme , Factores de Riesgo , Prevalencia , Tomografía de Coherencia Óptica , Adulto
3.
Br Dent J ; 229(8): 527-531, 2020 10.
Artículo en Inglés | MEDLINE | ID: mdl-33097886

RESUMEN

First trimester miscarriage is common, occurring in approximately 6.4-12.0% of pregnancies. Women who experience first trimester miscarriage will often have no other significant health conditions and the healthcare professional they most frequently visit could be their dentist or dental care professional. For this reason, it is important that the dental team is aware of the management of first trimester miscarriage in order to allow for a better understanding of the patient's experience and situation. The choice of language used by healthcare professionals with patients who are grieving is also important to ensure effective and open communication.This article aims to provide the dental team with knowledge of first trimester miscarriage, how the effects of this can be relevant within the dental setting, and how to communicate effectively and appropriately with patients who have experienced this traumatic event.


Asunto(s)
Aborto Espontáneo , Aborto Espontáneo/terapia , Femenino , Humanos , Atención al Paciente , Embarazo , Primer Trimestre del Embarazo
4.
Obstet Med ; 10(2): 58-60, 2017 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-28680463

RESUMEN

A nulliparous woman presented at 21 weeks' gestation with a 72-h history of a rash on her left arm. Initially isolated to the forearm, it had quickly spread, becoming multiple itchy fluid-filled blisters. Blood tests showed mild neutrophilia and raised CRP. Skin swabs demonstrated the presence of herpes simplex virus type 1 (HSV1) DNA. There was no history of previous HSV1 exposure. There is scant literature on uncomplicated cutaneous HSV1 since the majority is oral/genital. The incidence of transmission varies and is dependent on site of infection and immunological status. Type-specific serological testing is recommended to identify a primary first episode infection due to the 30-60% vertical transmission rate. Infection is associated with morbidity and mortality for both mother and fetus including maternal encephalitis, acute retinal necrosis, pneumonia and hepatitis. Neonatal disease can be congenital (cutaneous lesions, microcephaly, hydranencephaly, intracranial calcifications, chorioretinitis, microphthalmia and optic nerve atrophy) or acquired (skin, eyes and mouth disease or central nervous system disease or disseminated disease). Prophylactic aciclovir reduces the number of women with active genital lesions at the time of delivery. If primary infection occurs outside of the first trimester and active genital lesions are present, then vaginal delivery should be avoided. If infection has occurred in the first trimester, vaginal birth can be attempted even in the presence of active lesions. There is no available guidance on prophylactic treatment of non-genital HSV1 in pregnancy.

5.
J Control Release ; 223: 215-223, 2016 Feb 10.
Artículo en Inglés | MEDLINE | ID: mdl-26732555

RESUMEN

Prostate cancer, once it has progressed from its local to metastatic form, is a disease with poor prognosis and limited treatment options. Here we demonstrate an approach using nanoscale liposomes conjugated with E-selectin adhesion protein and Apo2L/TRAIL (TNF-related apoptosis-inducing ligand) apoptosis ligand that attach to the surface of leukocytes and rapidly clear viable cancer cells from circulating blood in the living mouse. For the first time, it is shown that such an approach can be used to prevent the spontaneous formation and growth of metastatic tumors in an orthotopic xenograft model of prostate cancer, by greatly reducing the number of circulating tumor cells. We conclude that the use of circulating leukocytes as a carrier for the anti-cancer protein TRAIL could be an effective tool to directly target circulating tumor cells for the prevention of prostate cancer metastasis, and potentially other cancers that spread through the bloodstream.


Asunto(s)
Selectina E/administración & dosificación , Leucocitos , Células Neoplásicas Circulantes/efectos de los fármacos , Neoplasias de la Próstata/tratamiento farmacológico , Ligando Inductor de Apoptosis Relacionado con TNF/administración & dosificación , Animales , Selectina E/uso terapéutico , Humanos , Leucocitos/metabolismo , Liposomas , Masculino , Ratones Transgénicos , Metástasis de la Neoplasia/prevención & control , Neoplasias de la Próstata/metabolismo , Neoplasias de la Próstata/patología , Ligando Inductor de Apoptosis Relacionado con TNF/uso terapéutico , Ensayos Antitumor por Modelo de Xenoinjerto
6.
J Endod ; 39(1): 57-61, 2013 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-23228258

RESUMEN

INTRODUCTION: Camphorquinone (CQ) is a photoinitiator that triggers polymerization of light-curing materials such as dental adhesives and composites. CQ does not become a part of the polymer network, suggesting that CQ can be leached out into surrounding environment including dental pulp and exert adversary effects on tissues. In order to understand the mechanisms of CQ-induced side effects, we investigated the effect of CQ on cell viability, cytokine secretion, and odontogenic differentiation of dental pulp stem cells in vitro. METHODS: Cell viability was assessed using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay after CQ exposure. Western blotting was performed for p16(INK4A), p21(WAF1), and p53. Secretory cytokines were evaluated using the membrane-enzyme-linked immunosorbent assay as well as conventional and quantitative reverse-transcription polymerase chain reaction. The effects of CQ on odontogenic differentiation were evaluated using alkaline phosphatase and alizarin red S staining methods. RESULTS: CQ treatment suppressed the proliferation of DPSCs and induced the expression of p16(INK4A), p21(WAF1), and p53. Levels of proinflammatory cytokines (eg, interleukin 6, interleukin 8, and matrix metalloproteinase-3 [MMP3]) were increased by CQ treatment. CQ also inhibited odontogenic differentiation and mineralization capacities of DPSC and MC3T3-E1 cells. CONCLUSIONS: Our study showed that CQ may trigger pulpal inflammation by inducing proinflammatory cytokine production from the pulpal cells and may impair odontogenic differentiation of dental pulp cells, resulting in pulpal irritation and inflammation.


Asunto(s)
Alcanfor/análogos & derivados , Citocinas/efectos de los fármacos , Pulpa Dental/efectos de los fármacos , Mediadores de Inflamación/metabolismo , Odontogénesis/efectos de los fármacos , Fotoiniciadores Dentales/toxicidad , Células 3T3 , Fosfatasa Alcalina/análisis , Animales , Antraquinonas , Western Blotting , Alcanfor/toxicidad , Diferenciación Celular/efectos de los fármacos , Supervivencia Celular/efectos de los fármacos , Colorantes , Inhibidor p16 de la Quinasa Dependiente de Ciclina/análisis , Inhibidor p21 de las Quinasas Dependientes de la Ciclina/análisis , Citocinas/metabolismo , Materiales Dentales/toxicidad , Pulpa Dental/citología , Humanos , Interleucina-6/análisis , Interleucina-8/análisis , Ensayo de Materiales , Metaloproteinasa 3 de la Matriz/análisis , Metacrilatos/toxicidad , Ratones , Sales de Tetrazolio , Tiazoles , Calcificación de Dientes/efectos de los fármacos , Proteína p53 Supresora de Tumor/análisis
7.
Am J Physiol Regul Integr Comp Physiol ; 292(1): R268-73, 2007 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-16990492

RESUMEN

Many gastrointestinal meal-related signals are transmitted to the central nervous system via the vagus nerve and thereby control changes in meal size. The c-Fos-positive neuron has been used as a marker of neuronal activation after lipid meals to examine the contribution of a selective macronutrient on brain neurocircuit activity. In rats fed Intralipid, the c-Fos-positive neurons were highly stimulated in the nucleus of the solitary tract (NTS) and in the hypothalamus, including the paraventricular nucleus (PVN), arcuate nucleus of the hypothalamus (ARC), and ventromedial hypothalamus at 4 h lipid feeding. However, c-Fos-like immunoreactivity was markedly attenuated in these brain regions when chylomicron formation/secretion was blocked by Pluronic L-81. After lymph was diverted from the lymph cannulated animals, the rats had a lower number of c-Fos-positive cells in the NTS and ARC. In contrast, the rats had higher c-Fos-positive neurons in PVN. The present study also revealed that c-Fos-positive neurons induced by feeding of Intalipid were abolished by CCK type 1 receptor antagonist, Lorglumide. We conclude that the formation and/or secretion of chylomicron are critical steps for initiating neuronal activation in the brain.


Asunto(s)
Química Encefálica/efectos de los fármacos , Lípidos/farmacología , Neuronas/metabolismo , Proteínas Proto-Oncogénicas c-fos/metabolismo , Animales , Núcleo Arqueado del Hipotálamo/efectos de los fármacos , Núcleo Arqueado del Hipotálamo/metabolismo , Encéfalo/citología , Encéfalo/efectos de los fármacos , Quilomicrones/biosíntesis , Emulsiones Grasas Intravenosas/administración & dosificación , Emulsiones Grasas Intravenosas/farmacología , Antagonistas de Hormonas/farmacología , Hipotálamo/efectos de los fármacos , Hipotálamo/metabolismo , Inmunohistoquímica , Intubación Gastrointestinal , Lípidos/administración & dosificación , Linfa/fisiología , Masculino , Núcleo Hipotalámico Paraventricular/efectos de los fármacos , Núcleo Hipotalámico Paraventricular/metabolismo , Poloxámero/farmacología , Proglumida/análogos & derivados , Proglumida/farmacología , Ratas , Ratas Sprague-Dawley , Receptores de Colecistoquinina/antagonistas & inhibidores , Receptores de Colecistoquinina/metabolismo , Núcleo Solitario/efectos de los fármacos , Núcleo Solitario/metabolismo , Tensoactivos/farmacología , Núcleo Hipotalámico Ventromedial/efectos de los fármacos , Núcleo Hipotalámico Ventromedial/metabolismo
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