Paulmyer-Lacroix O, Desbriere R, Poggi M, Achard V, Alessi M-C, Boudouresque F, Ouafik L'H, Vuaroqueaux V, Labuhn M, Dutourand A, Grino M
Inserm UMR 626, UFR de Médecine secteur Timone, 27 Bd Jean Moulin, 13385 Marseille cedex 5, France.
Eur J Endocrinol. 2006 Jul;155(1):177-85. doi: 10.1530/eje.1.02170.
Adrenomedullin (AM), a potent vasodilatator and antioxidative peptide, was shown recently to be expressed by adipose tissue. The aim of our study was to investigate the precise localization of AM within human adipose tissue, and to examine AM regulation in obesity.
Subcutaneous (SC) and omental (OM) adipose tissues from 9 lean and 13 obese women were profiled for AM expression changes. Preadipocytes from human adipose tissue were isolated and differentiated under defined adipogenic conditions.
AM expression was analyzed by immunohistochemistry, in situ hybridization and quantitative RT-PCR.
A strong AM expression was observed in vessel walls, stromal cell clusters and isolated stromal cells, some of them being CD 68 positive, whereas mature adipocytes were not labeled. Calcitonin receptor-like receptor and receptor activity-modifying proteins (RAMP) 2 and RAMP 3 were expressed in vessel walls. In vitro, preadipocytes of early differentiation stages spontaneously secreted AM. No difference in AM localization was found between SC and OM adipose tissue. AM levels in SC tissue did not differ between lean and obese subjects. By contrast, AM levels in OM tissue were significantly higher in obese as compared with lean women. Moreover, we found a positive relationship between OM AM and tumor necrosis factor alpha mRNA levels and AM-immunoreactive area in OM tissue followed the features of the metabolic syndrome.
Stromal cells from human adipose tissue, including macrophages, produce AM. Its synthesis increased in the OM territory during obesity and paralleled the features of the metabolic syndrome. Therefore, AM should be considered as a new member of the adipokine family.
肾上腺髓质素(AM)是一种强效血管舒张肽和抗氧化肽,最近研究表明其由脂肪组织表达。本研究旨在探究AM在人体脂肪组织中的精确定位,并研究肥胖状态下AM的调节情况。
对9名瘦女性和13名肥胖女性的皮下(SC)和网膜(OM)脂肪组织进行AM表达变化分析。在特定的成脂条件下分离并分化人脂肪组织中的前脂肪细胞。
采用免疫组织化学、原位杂交和定量逆转录聚合酶链反应分析AM表达。
在血管壁、基质细胞簇和分离的基质细胞中观察到强烈的AM表达,其中一些基质细胞CD 68呈阳性,而成熟脂肪细胞未被标记。降钙素受体样受体以及受体活性修饰蛋白(RAMP)2和RAMP 3在血管壁中表达。在体外,早期分化阶段的前脂肪细胞自发分泌AM。SC和OM脂肪组织之间在AM定位上未发现差异。SC组织中AM水平在瘦人和肥胖受试者之间无差异。相比之下,肥胖女性OM组织中的AM水平显著高于瘦女性。此外,我们发现OM组织中的AM与肿瘤坏死因子α mRNA水平呈正相关,且OM组织中AM免疫反应区域符合代谢综合征的特征。
人体脂肪组织中的基质细胞,包括巨噬细胞,可产生AM。在肥胖过程中,其在OM区域的合成增加,且与代谢综合征的特征平行。因此,AM应被视为脂肪因子家族的新成员。