De Vicente J C, Garcia-Suárez O, Esteban I, Santamaria J, Vega J A
Departamento de Cirugia, Universidad de Oviedo, Spain.
Ann Anat. 1998 Apr;180(2):157-63. doi: 10.1016/S0940-9602(98)80016-2.
This study was undertaken to analyze the occurrence of low- (p75) and high-affinity (TrkA, TrkB and TrkC) neurotrophin receptor proteins in human and mouse salivary glands using immunohistochemistry. Furthermore, the presence of neurotrophins was also investigated. The study was carried out on 14 human (4 parotid, 6 submandibular and 4 sublingual glands) and 5 mouse salivary glands, using polyclonal antibodies against Trk proteins. The intensity of immunostaining was calculated automatically and evaluated in arbitrary units of grey levels. In human tissues no immunoreactivity (IR) for the assessed antigens was observed in the serous or mucous acinar cells, although TrkA IR was found in the acini of the submandibular gland. The cells of the intercalated ducts showed p75 IR (sublingual) and TrkA IR (parotid gland). The striated and excretory ducts displayed p75 IR, TrkA IR and TrkC IR in all glands, but TrkB IR was never detected. No neurotrophins were detected. In the mouse glands the ductal cells display IR for p75 (submandibular) and Trks A and C (parotid and submandibular) but not the sublingual gland. Acinar cells of the submandibular gland also show p75 IR. The only neurotrophin found in the mouse salivary glands was NGF (submandibular gland). These results suggest that neurotrophins may be involved in controlling the physiology of epithelial salivary cells.
本研究旨在利用免疫组织化学分析人及小鼠唾液腺中低亲和力(p75)和高亲和力(TrkA、TrkB和TrkC)神经营养因子受体蛋白的表达情况。此外,还对神经营养因子的存在情况进行了研究。该研究对14例人唾液腺(4例腮腺、6例颌下腺和4例舌下腺)和5例小鼠唾液腺进行,使用针对Trk蛋白的多克隆抗体。免疫染色强度通过自动计算,并以任意灰度单位进行评估。在人体组织中,浆液性腺泡细胞或黏液性腺泡细胞未观察到所评估抗原的免疫反应性(IR),尽管在颌下腺的腺泡中发现了TrkA IR。闰管细胞显示p75 IR(舌下腺)和TrkA IR(腮腺)。所有腺体的纹状管和排泄管均显示p75 IR、TrkA IR和TrkC IR,但未检测到TrkB IR。未检测到神经营养因子。在小鼠腺体中,导管细胞显示p75 IR(颌下腺)以及TrkA和TrkC IR(腮腺和颌下腺),但舌下腺未显示。颌下腺的腺泡细胞也显示p75 IR。在小鼠唾液腺中发现的唯一神经营养因子是神经生长因子(NGF)(颌下腺)。这些结果表明,神经营养因子可能参与调控唾液腺上皮细胞的生理功能。