10 research outputs found

    Infrared thermography for convective heat transfer measurements

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    Human mesenchymal stem cells favour healing of the cutaneous radiation syndrome in a xenogenic transplant model

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    It has been suggested that human mesenchymal stem cells (hMSC) could be used to repair numerous injured tissues. We have studied the potential use of hMSC to limit radiation-induced skin lesions. Immunodeficient NOD/ SCID mice were locally irradiated to the leg (30 Gy, dose rate 2.7 Gy/min) using a 60Co source to induce a severe skin lesion. Cultured bone marrow hMSC were delivered intravenously to the mice. The irradiated skin samples were studied for the presence of the human cells, the severity of the lesions and the healing process. Macroscopic analysis and histology results showed that the lesions were evolving to a less severe degree of radiation dermatitis after hMSC transplant when compared to irradiated non-transplanted controls. Clinical scores for the studied skin parameters of treated mice were significantly improved. A faster healing was observed when compared to untreated mouse. Immunohistology and polymerase chain reaction analysis provided evidence that the human cells were found in the irradiated area. These results suggest a possible use of hMSC for the treatment of the early phase of the cutaneous radiation syndrome. A successful transplant of stem cells and subsequent reduction in radiation-induced complication may open the road to completely new strategies in cutaneous radiation syndrome therapy. © Springer-Verlag 2006

    Les cellules souches mésenchymateuses favorisent la cicatrisation des lésions cutanées radio induites

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    De nombreuses Ă©tudes suggĂšrent que les cellules souches adultes et plus particuliĂšrement les cellules souches MĂ©senchymateuses humaines (CSMh) pourraient ĂȘtre utilisĂ©es pour rĂ©parer de nombreux organes. Nous avons Ă©tudiĂ© la capacitĂ© des CSMh Ă  rĂ©duire les lĂ©sions cutanĂ©es radio induite. Pour induire des lĂ©sions sĂ©vĂšres de la peau, des souris NOD/SCID ont Ă©tĂ© irradiĂ©es au niveau de la patte droite postĂ©rieure (30 Gy, dĂ©bit 2,7 Gy/mn) en utilisant une source gamma au 60Co. Les CSMh ont Ă©tĂ© injectĂ©es 24 heures aprĂšs irradiation par voie intraveineuse. La prĂ©sence de cellules humaines, la sĂ©vĂ©ritĂ© des lĂ©sions et les processus de cicatrisation ont Ă©tĂ© Ă©tudiĂ©s sur les Ă©chantillons de peau prĂ©levĂ©s de 3 Ă  8 semaines aprĂšs irradiation. Nous avons pu observer que chez les souris greffĂ©es avec des CSMh, le niveau d’atteinte cutanĂ©e radio induite est significativement plus faible. Les scores cliniques utilisĂ©s pour l’étude de l’évolution des lĂ©sions cutanĂ©es de la peau sont significativement amĂ©liorĂ©s et une cicatrisation plus rapide est observĂ©e en comparaison des souris non injectĂ©es. La prĂ©sence de cellules humaines a pu ĂȘtre dĂ©tectĂ©e par PCR quantitative dans les zones cutanĂ©es en cours de cicatrisation. Ces rĂ©sultats suggĂšrent premiĂšrement que les CSMh sont capables de coloniser la peau altĂ©rĂ©e par les rayonnements ionisants et deuxiĂšmement qu’elles accĂ©lĂšrent le processus de rĂ©paration de ce tissu limitant ainsi les complications tissulaires radio induites. La greffe de CSMh pourrait ĂȘtre un traitement thĂ©rapeutique efficace des phases prĂ©coces du syndrome cutanĂ© radio induit
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