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1.
Calcif Tissue Int ; 96(4): 359-69, 2015 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-25725805

RESUMEN

Vascular calcification is an important pathological condition associated with increased risk of cardiovascular mortality. Hydroxyapatite (HA) found in such deposits is the same polymorph of calcium (Ca) found in bone, indicating calcification may involve mechanisms akin to bone formation. Vascular smooth muscle cells (Vsmcs) have been shown to undergo phenotypic change to osteoblast-like cells. However, the mechanisms underlying this phenotypic change are unclear, and whether the stimulus to become osteogenic is a result of loss of mineralization inhibitors or early mineral deposits is not known. Our aim in this study is to identify mechanisms and signal transduction pathways that cause differentiation of Vsmcs into osteoblast-like cells in the presence of HA. We first characterized vascular origin of Vsmcs by studying the expression of smooth muscle cell markers: myosin heavy chain and smooth muscle actin along with SM22α at both mRNA and protein levels. Vsmcs grown on HA exhibited progressive change in cellular morphology at 3-, 7-, and 14-day time points. Culturing of Vsmcs on HA disc resulted in decrease in media Ca levels and increased expression of Ca-sensing receptor (CaSR) on Vsmcs resulting in upregulation of intracellular CaSR signaling leading to increased BMP-2 secretion. BMP-2 pathway mediated differentiation of Vsmcs to osteoblast-like cells shown by expression of osteogenic markers like runt-related transcription factor 2, osteocalcin, and alkaline phosphatase at mRNA and protein levels. Blocking CaSR by NPS-2143 reduced BMP-2 secretion and blocking the BMP-2 pathway by LDN-193189, a BMP inhibitor, modulated expression of osteogenic markers confirming their role in osteogenesis of Vsmcs.


Asunto(s)
Aorta/citología , Proteína Morfogenética Ósea 2/metabolismo , Durapatita/química , Miocitos del Músculo Liso/efectos de los fármacos , Proteína Smad5/metabolismo , Animales , Técnicas de Cultivo de Célula , Diferenciación Celular/efectos de los fármacos , Regulación de la Expresión Génica , Naftalenos/química , Osteoblastos/citología , Osteocalcina/metabolismo , Osteogénesis , Reacción en Cadena de la Polimerasa , Polvos , Pirazoles/química , Pirimidinas/química , ARN Mensajero/metabolismo , Ratas , Receptores Sensibles al Calcio/metabolismo , Transducción de Señal , Stents
2.
J Exp Biol ; 217(Pt 12): 2130-8, 2014 Jun 15.
Artículo en Inglés | MEDLINE | ID: mdl-24920837

RESUMEN

Fluid-feeding Lepidoptera use an elongated proboscis, conventionally modeled as a drinking straw, to feed from pools and films of liquid. Using the monarch butterfly, Danaus plexippus (Linnaeus), we show that the inherent structural features of the lepidopteran proboscis contradict the basic assumptions of the drinking-straw model. By experimentally characterizing permeability and flow in the proboscis, we show that tapering of the food canal in the drinking region increases resistance, significantly hindering the flow of fluid. The calculated pressure differential required for a suction pump to support flow along the entire proboscis is greater than 1 atm (~101 kPa) when the butterfly feeds from a pool of liquid. We suggest that behavioral strategies employed by butterflies and moths can resolve this paradoxical pressure anomaly. Butterflies can alter the taper, the interlegular spacing and the terminal opening of the food canal, thereby controlling fluid entry and flow, by splaying the galeal tips apart, sliding the galeae along one another, pulsing hemolymph into each galeal lumen, and pressing the proboscis against a substrate. Thus, although physical construction of the proboscis limits its mechanical capabilities, its functionality can be modified and enhanced by behavioral strategies.


Asunto(s)
Mariposas Diurnas/fisiología , Modelos Biológicos , Estructuras Animales/anatomía & histología , Estructuras Animales/fisiología , Estructuras Animales/ultraestructura , Animales , Mariposas Diurnas/anatomía & histología , Mariposas Diurnas/ultraestructura , Conducta Alimentaria , Microscopía Electrónica de Rastreo , Permeabilidad , Presión
3.
Langmuir ; 29(33): 10596-602, 2013 Aug 20.
Artículo en Inglés | MEDLINE | ID: mdl-23875644

RESUMEN

We developed a novel technique enabling determination of the permeability of electrospun yarns composed of hundreds of fibers. Analyzing the wicking kinetics in a yarn-in-a-tube composite conduit, it was found that the kinetic is very specific. The liquid was pulled by the capillary pressure associated with the meniscus in the tube while the main resistance comes from the yarn. Therefore, one can separate the yarn permeability from the capillary pressure, which cannot be done in wicking experiments with single yarns. A surface tensiometer (Cahn) was employed to collect the data on wicking kinetics of hexadecane into the yarn-in-a-tube conduits. Yarns from different polymers and blends were electrospun and characterized using the proposed protocol. We showed that the permeability of electrospun yarns can be varied in a broad range from 10(-14) m(2) to 10(-12) m(2) by changing the fiber diameter and packing density. These results offer new applications of electrospun yarns as flexible micro- and nanofluidic systems.

4.
Nanoscale ; 3(11): 4685-95, 2011 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-21994037

RESUMEN

We describe a method of fabrication of nanoporous flexible probes which work as artificial proboscises. The challenge of making probes with fast absorption rates and good retention capacity was addressed theoretically and experimentally. This work shows that the probe should possess two levels of pore hierarchy: nanopores are needed to enhance the capillary action and micrometer pores are required to speed up fluid transport. The model of controlled fluid absorption was verified in experiments. We also demonstrated that the artificial proboscises can be remotely controlled by electric or magnetic fields. Using an artificial proboscis, one can approach a drop of hazardous liquid, absorb it and safely deliver it to an analytical device. With these materials, the paradigm of a stationary microfluidic platform can be shifted to the flexible structures that would allow one to pack multiple microfluidic sensors into a single fiber.


Asunto(s)
Microquímica/instrumentación , Micromanipulación/instrumentación , Nanoestructuras/química , Nanoestructuras/ultraestructura , Nanotecnología/instrumentación , Soluciones/aislamiento & purificación , Manejo de Especímenes/instrumentación , Absorción , Diseño de Equipo , Análisis de Falla de Equipo , Micromanipulación/métodos , Tamaño de la Partícula , Manejo de Especímenes/métodos
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