Kong L, Robinson C P, Peck A B, Vela-Roch N, Sakata K M, Dang H, Talal N, Humphreys-Beher M G
Department of Medicine, University of Texas Health Science Center, San Antonio, USA.
Clin Exp Rheumatol. 1998 Nov-Dec;16(6):675-81.
The lesion is Sjögren's syndrome consists of lymphocytic infiltration and has a pathology characteristic of the potential apoptotic death of salivary gland secretory epithelial cells. To examine the role of the glandular epithelial cells in the pathogenesis of autoimmune exocrinopathy, we studied Fas and Fas ligand (FasL) expression and quantitated the levels of apoptosis in salivary and lacrimal glands from NOD and NOD-scid mice, an animal model that develops a Sjögren's syndrome-like pathology.
The parotid, submandibular and lacrimal tissues of NOD, NOD-scid, and BALB/c mice were evaluated by immunohistochemical analysis for the expression of Fas and FasL. Nuclear fragmentation of DNA from the epithelial cells of exocrine tissues was evaluated by the terminal UTP nucleotide end labeling method (TUNEL). Messenger RNA was isolated from 8 and 18 week old mice and was analyzed by the reverse transcription-polymerase chain reaction (RT-PCR) for the expression of Fas and FasL.
We found suggestive evidence that apoptosis of the secretory epithelial cells occurs in both NOD and NOD-scid mice despite the lack of T- and B-lymphocytes in the latter. FasL mRNA and cell surface protein were expressed in salivary and lacrimal gland epithelial cells from 8 and 18 week old NOD, NOD-scid, and BALB/c mice. Fas protein and mRNA were expressed only in the exocrine glands from 18 week old NOD and NOD-scid mice. Glandular secretory epithelial cell apoptosis was elevated in both NOD and NOD-scid mice, however; there was little evidence of apoptosis in the control strain of BALB/c mice.
These results suggest a potential apoptotic process dependent on Fas:FasL interactions occurring in NOD-scid glandular secretory epithelial cells in the absence of lymphocytic infiltration.
干燥综合征的病变包括淋巴细胞浸润,具有唾液腺分泌上皮细胞潜在凋亡死亡的病理特征。为研究腺上皮细胞在自身免疫性外分泌病发病机制中的作用,我们研究了Fas和Fas配体(FasL)的表达,并对非肥胖糖尿病(NOD)小鼠和NOD-scid小鼠(一种发生类似干燥综合征病理的动物模型)的唾液腺和泪腺中的凋亡水平进行了定量分析。
通过免疫组织化学分析评估NOD、NOD-scid和BALB/c小鼠的腮腺、颌下腺和泪腺组织中Fas和FasL的表达。采用末端脱氧核苷酸转移酶介导的缺口末端标记法(TUNEL)评估外分泌组织上皮细胞DNA的核片段化。从8周龄和18周龄小鼠中分离信使核糖核酸(mRNA),并通过逆转录聚合酶链反应(RT-PCR)分析Fas和FasL的表达。
我们发现有提示性证据表明,尽管NOD-scid小鼠缺乏T淋巴细胞和B淋巴细胞,但NOD小鼠和NOD-scid小鼠的分泌上皮细胞均发生凋亡。8周龄和18周龄的NOD、NOD-scid和BALB/c小鼠的唾液腺和泪腺上皮细胞中均表达FasL mRNA和细胞表面蛋白。Fas蛋白和mRNA仅在18周龄的NOD和NOD-scid小鼠的外分泌腺中表达。然而,NOD小鼠和NOD-scid小鼠的腺分泌上皮细胞凋亡均增加;在对照品系的BALB/c小鼠中几乎没有凋亡证据。
这些结果表明,在无淋巴细胞浸润的情况下,NOD-scid腺分泌上皮细胞中可能存在依赖Fas:FasL相互作用的凋亡过程。