Changes in Rab3D Expression and Distribution in the Acini of Sjogren's Syndrome Patients Are Associated With Loss of Cell Polarity and Secretory Dysfunction

被引:40
作者
Bahamondes, Veronica
Albornoz, Amelina
Aguilera, Sergio [2 ]
Alliende, Cecilia
Molina, Claudio [3 ]
Castro, Isabel
Urzua, Ulises
Quest, Andrew F. G.
Barrera, Maria-Jose
Gonzalez, Sergio [3 ,4 ]
Sanchez, Marianela
Haertel, Steffen
Hermoso, Marcela
Leyton, Cecilia
Gonzalez, Maria-Julieta [1 ]
机构
[1] Univ Chile, Fac Med, Inst Ciencias Biomed, Santiago 7, Chile
[2] Indisa Clin, Santiago, Chile
[3] Mayor Univ, Santiago, Chile
[4] San Sebastian Univ, Santiago, Chile
来源
ARTHRITIS AND RHEUMATISM | 2011年 / 63卷 / 10期
关键词
SALIVARY-GLANDS; GOLGI-COMPLEX; BASAL LAMINA; LOCALIZATION; MEMBRANE; PROTEINS; XEROSTOMIA; BINDING; MUC5B; MODEL;
D O I
10.1002/art.30500
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Objective. Oral and ocular dryness are frequent and serious symptoms of Sjogren's syndrome (SS) that reflect problems in secretion due to glandular dysfunction. Exocytosis, an important process in the secretory pathway, requires the participation of Rab family GTPases. This study was undertaken to analyze the expression and localization of Rab3D and Rab8A and to examine their correlation with acinar cell polarity and glandular secretory function. Methods. Nineteen patients with SS and 17 controls were evaluated. Levels of Rab3D and Rab8A messenger RNA (mRNA) and protein were determined by real-time polymerase chain reaction and Western blotting. Subcellular localization of proteins was determined by indirect immunofluorescence analysis. Results. In patients with SS, total Rab3D protein levels decreased significantly, while mRNA levels remained unchanged. For Rab8A, no changes in either mRNA or protein levels were detected. In serous acini of labial salivary glands from patients with SS, the following 4 patterns of Rab3D staining were distinguishable: severely decreased, distribution throughout the cytoplasm, distribution throughout the cytoplasm combined with loss of nuclear polarity, and normal apical localization. Basal localization of Rab8A was not modified. Rab3D changes were accompanied by apicobasolateral redistribution of ezrin, loss of nuclear polarity, thicker Golgi stacks, and mucin 7 accumulation in the cytoplasm. Finally, low Rab3D protein levels correlated with alterations in scintigraphy measurements. Conclusion. Our findings indicate that Rab3D regulates the exocytosis of many components critical for the maintenance of oral physiology. Hence, the changes observed in Rab3D expression and distribution are likely to contribute to the decrease in or loss of saliva components (i.e., mucins), which may explain the variety of oral and ocular symptoms associated with SS.
引用
收藏
页码:3126 / 3135
页数:10
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