Zi-Jian Yang, Shou-Yue Huang, Yu-Feng Zhou, Shun-Chang Sun
{"title":"在小鼠体内敲除 TMEM206 会导致角膜透明度下降。","authors":"Zi-Jian Yang, Shou-Yue Huang, Yu-Feng Zhou, Shun-Chang Sun","doi":"10.18240/ijo.2024.11.01","DOIUrl":null,"url":null,"abstract":"<p><strong>Aim: </strong>To investigate the role of transmembrane protein 206 (TMEM206) in corneal edema in mice by knockout the <i>TMEM206</i> gene using CRISPR/Cas9 editing technology.</p><p><strong>Methods: </strong><i>TMEM206</i>-knockout mice were generated using the CRISPR-Cas9 system. Variations in ophthalmic pathology were observed using slit lamp microscope and optical coherence tomography (OCT), intraocular pressure (IOP) was measured using a TonoLab Rebound Tonometer, and the ultrastructure of the corneal was observed using a transmission electron microscope.</p><p><strong>Results: </strong>Corneal opacity was observed in 4/18 homozygous <i>TMEM206<sup>-/-</sup></i> mice whereas a similar change was not observed in heterozygous <i>TMEM206<sup>+/-</sup></i> mice and wild-type littermates. OCT examination showed that the mean central cornea thickness was 125±5.4 µm in 4 homozygous <i>TMEM206<sup>-/-</sup></i> mice developed corneal edema and 115±1.2 µm in wild-type mice (<i>t</i>=3.468, <i>P</i><0.05) at 43wk. The mean IOP was 12.08±0.07 mm Hg in four right eyes with corneal edema and 12.03±0.03 mm Hg in three normal left eyes (<i>P</i>>0.05). Transmission electron microscopy revealed a disruption in the organization of the collagen fibrils in the central part of the cornea in homozygous <i>TMEM206<sup>-/-</sup></i> mice.</p><p><strong>Conclusion: </strong>TMEM206 is associated with corneal edema which caused organizational disruption of collagen fibrils in corneas of mice.</p>","PeriodicalId":14312,"journal":{"name":"International journal of ophthalmology","volume":"17 11","pages":"1967-1972"},"PeriodicalIF":1.9000,"publicationDate":"2024-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11528273/pdf/","citationCount":"0","resultStr":"{\"title\":\"Knockout of <i>TMEM206</i> in mice associated with a loss of corneal transparency.\",\"authors\":\"Zi-Jian Yang, Shou-Yue Huang, Yu-Feng Zhou, Shun-Chang Sun\",\"doi\":\"10.18240/ijo.2024.11.01\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Aim: </strong>To investigate the role of transmembrane protein 206 (TMEM206) in corneal edema in mice by knockout the <i>TMEM206</i> gene using CRISPR/Cas9 editing technology.</p><p><strong>Methods: </strong><i>TMEM206</i>-knockout mice were generated using the CRISPR-Cas9 system. Variations in ophthalmic pathology were observed using slit lamp microscope and optical coherence tomography (OCT), intraocular pressure (IOP) was measured using a TonoLab Rebound Tonometer, and the ultrastructure of the corneal was observed using a transmission electron microscope.</p><p><strong>Results: </strong>Corneal opacity was observed in 4/18 homozygous <i>TMEM206<sup>-/-</sup></i> mice whereas a similar change was not observed in heterozygous <i>TMEM206<sup>+/-</sup></i> mice and wild-type littermates. OCT examination showed that the mean central cornea thickness was 125±5.4 µm in 4 homozygous <i>TMEM206<sup>-/-</sup></i> mice developed corneal edema and 115±1.2 µm in wild-type mice (<i>t</i>=3.468, <i>P</i><0.05) at 43wk. The mean IOP was 12.08±0.07 mm Hg in four right eyes with corneal edema and 12.03±0.03 mm Hg in three normal left eyes (<i>P</i>>0.05). Transmission electron microscopy revealed a disruption in the organization of the collagen fibrils in the central part of the cornea in homozygous <i>TMEM206<sup>-/-</sup></i> mice.</p><p><strong>Conclusion: </strong>TMEM206 is associated with corneal edema which caused organizational disruption of collagen fibrils in corneas of mice.</p>\",\"PeriodicalId\":14312,\"journal\":{\"name\":\"International journal of ophthalmology\",\"volume\":\"17 11\",\"pages\":\"1967-1972\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2024-11-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11528273/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International journal of ophthalmology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.18240/ijo.2024.11.01\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"OPHTHALMOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of ophthalmology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.18240/ijo.2024.11.01","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"OPHTHALMOLOGY","Score":null,"Total":0}
Knockout of TMEM206 in mice associated with a loss of corneal transparency.
Aim: To investigate the role of transmembrane protein 206 (TMEM206) in corneal edema in mice by knockout the TMEM206 gene using CRISPR/Cas9 editing technology.
Methods: TMEM206-knockout mice were generated using the CRISPR-Cas9 system. Variations in ophthalmic pathology were observed using slit lamp microscope and optical coherence tomography (OCT), intraocular pressure (IOP) was measured using a TonoLab Rebound Tonometer, and the ultrastructure of the corneal was observed using a transmission electron microscope.
Results: Corneal opacity was observed in 4/18 homozygous TMEM206-/- mice whereas a similar change was not observed in heterozygous TMEM206+/- mice and wild-type littermates. OCT examination showed that the mean central cornea thickness was 125±5.4 µm in 4 homozygous TMEM206-/- mice developed corneal edema and 115±1.2 µm in wild-type mice (t=3.468, P<0.05) at 43wk. The mean IOP was 12.08±0.07 mm Hg in four right eyes with corneal edema and 12.03±0.03 mm Hg in three normal left eyes (P>0.05). Transmission electron microscopy revealed a disruption in the organization of the collagen fibrils in the central part of the cornea in homozygous TMEM206-/- mice.
Conclusion: TMEM206 is associated with corneal edema which caused organizational disruption of collagen fibrils in corneas of mice.
期刊介绍:
· International Journal of Ophthalmology-IJO (English edition) is a global ophthalmological scientific publication
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