Experimental Dento-Maxillo-Facial Medicine, University of Bonn, 53111 Bonn, Germany ; Clinical Research Unit 208, University of Bonn, 53111 Bonn, Germany.
Clinical Research Unit 208, University of Bonn, 53111 Bonn, Germany.
Int J Endocrinol. 2014;2014:180304. doi: 10.1155/2014/180304. Epub 2014 Jul 22.
Obesity is increasing throughout the globe and characterized by excess adipose tissue, which represents a complex endocrine organ. Adipose tissue secrets bioactive molecules called adipokines, which act at endocrine, paracrine, and autocrine levels. Obesity has recently been shown to be associated with periodontitis, a disease characterized by the irreversible destruction of the tooth-supporting tissues, that is, periodontium, and also with compromised periodontal healing. Although the underlying mechanisms for these associations are not clear yet, increased levels of proinflammatory adipokines, such as leptin, as found in obese individuals, might be a critical pathomechanistic link. The objective of this study was to examine the impact of leptin on the regenerative capacity of human periodontal ligament (PDL) cells and also to study the local leptin production by these cells. Leptin caused a significant downregulation of growth (TGFβ1, and VEGFA) and transcription (RUNX2) factors as well as matrix molecules (collagen, and periostin) and inhibited SMAD signaling under regenerative conditions. Moreover, the local expression of leptin and its full-length receptor was significantly downregulated by inflammatory, microbial, and biomechanical signals. This study demonstrates that the hormone leptin negatively interferes with the regenerative capacity of PDL cells, suggesting leptin as a pathomechanistic link between obesity and compromised periodontal healing.
肥胖症在全球范围内不断增加,其特征是脂肪组织过多,脂肪组织代表着一种复杂的内分泌器官。脂肪组织分泌生物活性分子,称为脂肪因子,它们在内分泌、旁分泌和自分泌水平上发挥作用。最近的研究表明,肥胖与牙周炎有关,牙周炎是一种以牙齿支持组织(即牙周组织)不可逆破坏为特征的疾病,也与牙周愈合受损有关。虽然这些关联的潜在机制尚不清楚,但在肥胖个体中发现的促炎脂肪因子(如瘦素)水平升高可能是一个关键的病理机制联系。本研究旨在研究瘦素对人牙周韧带(PDL)细胞再生能力的影响,并研究这些细胞的局部瘦素产生。瘦素在再生条件下导致生长(TGFβ1 和 VEGFA)和转录(RUNX2)因子以及基质分子(胶原和骨膜蛋白)的显著下调,并抑制 SMAD 信号转导。此外,炎症、微生物和生物力学信号显著下调了瘦素及其全长受体的局部表达。本研究表明,激素瘦素会对 PDL 细胞的再生能力产生负面影响,提示瘦素是肥胖与牙周愈合受损之间的病理机制联系。