J Korean Ophthalmol Soc > Volume 55(8); 2014 > Article
Journal of the Korean Ophthalmological Society 2014;55(8):1187-1194.
DOI: https://doi.org/10.3341/jkos.2014.55.8.1187    Published online August 15, 2014.
Transmission Electron Microscopic Findings of Lacrimal Gland Acinar Cells Induced by In Vivo Dry Eye.
Yu Ri Seo, A Reum Yeo, Hye Mi Noh, Dong Yong Chung, Tae Im Kim, Kyoung Yul Seo, Eung Kweon Kim, Hyung Keun Lee
1Institute of Vision Research, Department of Ophthalmology, Yonsei University College of Medicine, Seoul, Korea. shadik@yuhs.ac
2Morphology Lab., Yonsei Biomedical Research Institute, Seoul, Korea.
3Institute of Corneal Dystrophy Research, Department of Ophthalmology, Yonsei University College of Medicine, Seoul, Korea.
투과전자현미경을 이용하여 관찰한 건성안 유발 마우스 눈물샘 선세포의 변화
서유리1⋅여아름1⋅노혜미1⋅정동룡2⋅김태임1,3⋅서경률1,3⋅김응권1,3⋅이형근1,3
Institute of Vision Research, Department of Ophthalmology, Yonsei University College of Medicine1, Seoul, Korea
Morphology Lab., Yonsei Biomedical Research Institute2, Seoul, Korea
Institute of Corneal Dystrophy Research, Department of Ophthalmology, Yonsei University College of Medicine3, Seoul, Korea
Abstract
PURPOSE
To determine the change in lacrimal gland (LG) acinar cells induced by in vivo dry eye (DE). METHODS: Six to 8-week-old (C57BL/6) mice were placed in a controlled environment chamber at <20% humidity for 2 weeks, and a control group was bred in a normal environment. After these 2 weeks of dry eye (DE) induction, the mice were sacrificed and their LGs were collected. Lacrimal gland acinar cell organelle structures were observed with Transmission Electron Microscopy (TEM). TEM images were analyzed using the Image J program. RESULTS: The size of the LGs of DE-induced mice decreased compared to those of normal mice. Terminal deoxynucleotidyl transferase dUTP Nick End Labeling (TUNEL) staining was negative in DE-induced LGs. Under the TEM, the endoplasmic reticulum (ER) lumen was dilated and the lumen density increased in DE-induced mice. Additionally, cell organelles were surrounded by elongated ER lumens. The mitochondrial structure was destroyed and the number of vacuoles increased in the LGs of DE-induced mice. CONCLUSIONS: Structural changes of the LG developed due to DE induction. This suggests that the detailed mechanisms of these changes were ER stress and autophagy. However, there were no definite signs of apoptosis in the acinar cells of the DE-induced LGs. These findings are regarded as an important clue of the pathogenesis of non-Sjogren-type dry eye.
Key Words: Autophagy;Dry eye;ER stress;Lacrimal gland


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