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Background

A bioartificial heart is a theoretical alternative to transplantation or mechanical left ventricular support. Native hearts decellularized with preserved architecture and vasculature may provide an acellular tissue platform for organ regeneration. We sought to develop a tissue-engineered whole-heart neoscaffold in human-sized porcine hearts.

Methods

We decellularized porcine hearts (n = 10) by coronary perfusion with ionic detergents in a modified Langendorff circuit. We confirmed decellularization by histology, transmission electron microscopy and fluorescence microscopy, quantified residual DNA by spectrophotometry, and evaluated biomechanical stability with ex-vivo left-ventricular pressure/volume studies, all compared to controls. We then mounted the decellularized porcine hearts in a bioreactor and reseeded them with murine neonatal cardiac cells and human umbilical cord derived endothelial cells (HUVEC) under simulated physiological conditions.

Results

Decellularized hearts lacked intracellular components but retained specific collagen fibers, proteoglycan, elastin and mechanical integrity; quantitative DNA analysis demonstrated a significant reduction of DNA compared to controls (82.6±3.2 ng DNA/mg tissue vs. 473.2±13.4 ng DNA/mg tissue, p<0.05). Recellularized porcine whole-heart neoscaffolds demonstrated re-endothelialization of coronary vasculature and measurable intrinsic myocardial electrical activity at 10 days, with perfused organ culture maintained for up to 3 weeks.

Conclusions

Human-sized decellularized porcine hearts provide a promising tissue-engineering platform that may lead to future clinical strategies in the treatment of heart failure.  相似文献   
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Roost  Thibaut  Schies  Jo-Ann  Girondot  Marc  Robin  Jean-Patrice  Lelong  Pierre  Martin  Jordan  Siegwalt  Flora  Jeantet  Lorène  Giraudeau  Mathieu  Le Loch  Guillaume  Bejarano  Manola  Bonola  Marc  Benhalilou  Abdelwahab  Murgale  Céline  Andreani  Lucas  Jacaria  François  Campistron  Guilhem  Lathière  Anthony  Martial  François  Hielard  Gaëlle  Arqué  Alexandre  Régis  Sidney  Lecerf  Nicolas  Frouin  Cédric  Lefebvre  Fabien  Aubert  Nathalie  Flora  Frédéric  Pimentel  Esteban  Lafolle  Rachelle  Thobor  Florence  Arthus  Mosiah  Etienne  Denis  Lecerf  Nathaël  Allenou  Jean-Pierre  Desigaux  Florian  Larcher  Eugène  Larcher  Christian  Curto  Alberto Lo  Befort  Joanne  Maceno-Panevel  Myriane  Lepori  Muriel  Chevallier  Pascale  Chevallier  Tao  Meslier  Stéphane  Landreau  Anthony  Habold  Caroline  Le Maho  Yvon  Chevallier  Damien 《EcoHealth》2022,19(2):190-202

Fibropapillomatosis (FP) threatens the survival of green turtle (Chelonia mydas) populations at a global scale, and human activities are regularly pointed as causes of high FP prevalence. However, the association of ecological factors with the disease’s severity in complex coastal systems has not been well established and requires further studies. Based on a set of 405 individuals caught over ten years, this preliminary study provides the first insight of FP in Martinique Island, which is a critical development area for immature green turtles. Our main results are: (i) 12.8% of the individuals were affected by FP, (ii) FP has different prevalence and temporal evolution between very close sites, (iii) green turtles are more frequently affected on the upper body part such as eyes (41.4%), fore flippers (21.9%), and the neck (9.4%), and (iv) high densities of individuals are observed on restricted areas. We hypothesise that turtle’s aggregation enhances horizontal transmission of the disease. FP could represent a risk for immature green turtles’ survival in the French West Indies, a critical development area, which replenishes the entire Atlantic population. Continuing scientific monitoring is required to identify which factors are implicated in this panzootic disease and ensure the conservation of the green turtle at an international scale.

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