Erratum to Heparan and chondroitin sulfate on growth plate perlecan mediate binding and delivery of FGF-2 to FGF receptors" [Matrix Biology 26 (2007) 175−184]
- 作者：Simone M.-L. Smith ; Leigh A. West ; Prasanthi Govindraj ; Xiuqin Zhang ; David M. Qrnitz ; John R. Hassell
- 关键词：Laminin ; Collagen ; Fibronectin ; Diabetes ; Salivary gland
- 刊名：Matrix Biology
- 出版年：2007
- 期刊代码：64_0945053x
- 类别：imm
- 出版时间：September 2007
- 卷：26
- 期：7
- 页码：583
- 文件大小：204 K
摘要
The majority of the oral manifestations of diabetes mellitus are secondary to a reduced salivary flow, whose causes are still poorly understood. In the kidney, diabetes complications involve increased Transforming Growth Factor β (TGFβ) production and the thickening of basement membrane in small vessels. By using immunohistochemistry and western blotting, we studied the expression and signaling of TGFβ and the distribution of extracellular matrix (ECM) proteins: laminin, fibronectin, collagens III, IV and V in the parotid gland of control and diabetic rats, 30 and 60 days after streptozotocin injection (D30 and D60). At D30, there was an important increase of laminin whereas fibronectin and collagen V were moderately augmented. At D60, an additional increase of all ECM proteins was observed. TGFβ1 expression was not affected at any time. In contrast, TGFβ2 levels were significantly higher at D30, concomitant with increased TGFβ receptor II (TβRII), phosphorylated Smads 2 and 3 (pSmads 2–3) and Latent TGFβ Binding Protein 1 (LTBP1). At D60, TGFβ2 and TβRII were still increased, whereas phosphorylation of Smads was markedly decreased, and LTBP1 returned to control levels. In the control groups, TGFβ2 labeling was localized preferentially in ductal cells, whereas at D30 and D60 the staining was also observed in acinar cells. The same pattern of distribution was observed for pSmads 2–3 at D30, especially in nuclei. At D60, labeling was weak and dispersed throughout the cytoplasm. These data suggest that hyperglycaemia increases the deposition of ECM proteins in the rat parotid gland, possibly through augmentation of TGFβ2 expression and signaling.