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Microcirculation ; 31(6): e12873, 2024 08.
Artigo em Inglês | MEDLINE | ID: mdl-38953384

RESUMO

OBJECTIVE: Intravascular lymphatic valves often occur in proximity to vessel junctions. It is commonly held that disturbed flow at junctions is responsible for accumulation of valve-forming cells (VFCs) at these locations as the initial step in valve creation, and the one which explains the association with these sites. However, evidence in favor is largely limited to cell culture experiments. METHODS: We acquired images of embryonic lymphatic vascular networks from day E16.5, when VFC accumulation has started but the developing valve has not yet altered the local vessel geometry, stained for Prox1, which co-localizes with Foxc2. Using finite-element computational fluid mechanics, we simulated the flow through the networks, under conditions appropriate to this early development stage. Then we correlated the Prox1 distributions with the distributions of simulated fluid shear and shear stress gradient. RESULTS: Across a total of 16 image sets, no consistent correlation was found between Prox1 distribution and the local magnitude of fluid shear, or its positive or negative gradient. CONCLUSIONS: This, the first direct semi-empirical test of the localization hypothesis to interrogate the tissue from in vivo at the critical moment of development, does not support the idea that a feature of the local flow determines valve localization.


Assuntos
Proteínas de Homeodomínio , Vasos Linfáticos , Proteínas Supressoras de Tumor , Animais , Vasos Linfáticos/embriologia , Vasos Linfáticos/fisiologia , Vasos Linfáticos/metabolismo , Proteínas de Homeodomínio/metabolismo , Proteínas Supressoras de Tumor/metabolismo , Camundongos , Fatores de Transcrição Forkhead/metabolismo , Hidrodinâmica , Modelos Biológicos , Embrião de Mamíferos
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