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酒精摄入对骨细胞细胞过程的影响:一项分子成像研究。

Effect of the alcohol consumption on osteocyte cell processes: a molecular imaging study.

作者信息

Maurel Delphine B, Benaitreau Delphine, Jaffré Christelle, Toumi Hechmi, Portier Hugues, Uzbekov Rustem, Pichon Chantal, Benhamou Claude L, Lespessailles Eric, Pallu Stéphane

机构信息

Laboratory of Oral Biology, School of Dentistry, Kansas City, MO, USA.

出版信息

J Cell Mol Med. 2014 Aug;18(8):1680-93. doi: 10.1111/jcmm.12113. Epub 2013 Aug 15.

Abstract

We have previously shown microarchitectural tissue changes with cellular modifications in osteocytes following high chronic alcohol dose. The aim of this study was to assess the dose effect of alcohol consumption on the cytoskeleton activity, the cellular lipid content and modulation of differentiation and apoptosis in osteocyte. Male Wistar rats were divided into three groups: Control (C), Alcohol 25% v/v (A25) or Alcohol 35% v/v (A35) for 17 weeks. Bone mineral density (BMD) was assessed by DXA, osteocyte empty lacunae, lacunae surface, bone marrow fat with bright field microscopy. Osteocyte lipid content was analysed with transmission electron microscopy (TEM) and epifluorescence microscopy. Osteocyte apoptosis was analysed with immunolabelling and TEM. Osteocyte differentiation and cytoskeleton activity were analysed with immunolabelling and real time quantitative PCR. At the end of the protocol, BMD was lower in A25 and A35 compared with C, while the bone marrow lipid content was increased in these groups. More empty osteocyte lacunae and osteocyte containing lipid droplets in A35 were found compared with C and A25. Cleaved caspase-3 staining and chromatin condensation were increased in A25 and A35 versus C. Cleaved caspase-3 was increased in A35 versus A25. CD44 and phosphopaxillin stainings were higher in A35 compared with C and A25. Paxillin mRNA expression was higher in A35 versus A25 and C and sclerostin mRNA expression was higher in A35 versus C. We only observed a dose effect of alcohol consumption on cleaved caspase-3 osteocyte immunostaining levels and on the number of lipid droplets in the bone marrow.

摘要

我们之前已经表明,长期高剂量饮酒后骨细胞会出现微观结构组织变化以及细胞改变。本研究的目的是评估饮酒对骨细胞骨架活性、细胞脂质含量以及分化和凋亡调节的剂量效应。将雄性Wistar大鼠分为三组:对照组(C)、25% v/v酒精组(A25)或35% v/v酒精组(A35),持续17周。通过双能X线吸收法(DXA)评估骨密度(BMD),用明场显微镜观察骨细胞空陷窝、陷窝表面、骨髓脂肪。用透射电子显微镜(TEM)和落射荧光显微镜分析骨细胞脂质含量。用免疫标记和TEM分析骨细胞凋亡。用免疫标记和实时定量PCR分析骨细胞分化和细胞骨架活性。在实验方案结束时,与C组相比,A25组和A35组的BMD较低,而这些组的骨髓脂质含量增加。与C组和A25组相比,A35组发现更多空的骨细胞陷窝和含有脂滴的骨细胞。与C组相比,A25组和A35组中裂解的半胱天冬酶-3染色和染色质凝聚增加。与A25组相比,A35组中裂解的半胱天冬酶-3增加。与C组和A25组相比,A35组中CD44和磷酸化桩蛋白染色更高。与A25组和C组相比,A35组中桩蛋白mRNA表达更高,与C组相比,A35组中硬化蛋白mRNA表达更高。我们仅观察到饮酒对裂解的半胱天冬酶-3骨细胞免疫染色水平和骨髓中脂滴数量有剂量效应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f16d/4190913/ba0bacfd7942/jcmm0018-1680-f1.jpg

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