Center for Salivary Gland Diseases and Center Laboratory, Peking University School and Hospital of Stomatology, Beijing, China.
PLoS One. 2013 May 7;8(5):e63878. doi: 10.1371/journal.pone.0063878. Print 2013.
Adiponectin and adiponectin receptors (AdipoR1/2) are expressed in various tissues and are involved in the regulation of multiple functions such as energy metabolism and inflammatory responses. However, the effect of adiponectin and AdipoRs in submandibular glands has not been fully evaluated. In the present study, we found that mRNA and protein of both adiponectin and AdipoR1/2 were expressed in rat submandibular glands and in the SMG-C6 cell line, as evidenced by RT-PCR and Western blot analysis. Immunofluorescence staining showed that adiponectin was diffused in the cytoplasm, while AdipoR1/2 was concentrated in the membrane of acinar cells. Saliva flow was significantly increased by full length adiponectin (fAd) or globular adiponectin (gAd) perfusion in isolated rat submandibular glands. 5-Aminoimidazole-4-carboxamide-1-4-ribofuranoside (AICAR), an adenosine monophosphate activated protein kinase (AMPK) activator, also increased saliva secretion. fAd, gAd, and AICAR all increased the average width of apical tight junctions in perfused submandibular glands, and decreased transepithelial electrical resistance (TER) in SMG-C6 cells, suggesting that adiponectin promoted secretion by modulating paracellular permeability. fAd and gAd increased p-AMPK levels, while AraA, an AMPK antagonist, abolished fAd- and gAd-induced changes in secretion, tight junction ultrastructure, and TER. Moreover, both AdipoR1 and AdipoR2 were required for fAd- or gAd-induced p-AMPK and TER responses, suggesting from their inhibition following AdipoR1 or AdipoR2 knockdown, and co-knockdown of AdipoRs by RNA interference. Our results suggest that adiponectin functions as a promoter of salivary secretion in rat submandibular glands via activation of AdipoRs, AMPK, and paracellular permeability.
脂联素和脂联素受体(AdipoR1/2)在各种组织中表达,并参与能量代谢和炎症反应等多种功能的调节。然而,脂联素和 AdipoRs 在颌下腺中的作用尚未得到充分评估。在本研究中,我们通过 RT-PCR 和 Western blot 分析发现,脂联素和 AdipoR1/2 的 mRNA 和蛋白均在大鼠颌下腺和 SMG-C6 细胞系中表达。免疫荧光染色显示,脂联素弥散在细胞质中,而 AdipoR1/2 则集中在腺泡细胞的膜上。全长脂联素(fAd)或球形脂联素(gAd)灌流离体大鼠颌下腺可显著增加唾液流量。腺苷单磷酸激活蛋白激酶(AMPK)激活剂 5-氨基咪唑-4-甲酰胺-1-β-D-呋喃核糖苷(AICAR)也增加了唾液分泌。fAd、gAd 和 AICAR 均增加了灌流颌下腺中顶端紧密连接的平均宽度,并降低了 SMG-C6 细胞中的跨上皮电阻(TER),表明脂联素通过调节细胞旁通透性促进分泌。fAd 和 gAd 增加了 p-AMPK 水平,而 AMPK 拮抗剂 AraA 则消除了 fAd 和 gAd 诱导的分泌、紧密连接超微结构和 TER 的变化。此外,AdipoR1 和 AdipoR2 均参与了 fAd 或 gAd 诱导的 p-AMPK 和 TER 反应,这从 AdipoR1 或 AdipoR2 敲低后以及 RNA 干扰共敲低 AdipoRs 后对其的抑制作用中得到证实。我们的结果表明,脂联素通过激活 AdipoRs、AMPK 和细胞旁通透性,作为大鼠颌下腺唾液分泌的促进剂发挥作用。