Ji Seung Jung, Hyo Youn Jo, Jiyi Hwang, Donghee Kim, Myeongjee Kwon, Jungyeon Yong, Haerin Yoon, Hyun Jik Lee, Kyung-Mee Park
{"title":"结膜下应用依维莫司和西罗莫司预处理的MSCs预防糖尿病视网膜病变的疗效。","authors":"Ji Seung Jung, Hyo Youn Jo, Jiyi Hwang, Donghee Kim, Myeongjee Kwon, Jungyeon Yong, Haerin Yoon, Hyun Jik Lee, Kyung-Mee Park","doi":"10.1167/tvst.14.9.19","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Diabetic retinopathy (DR) is a leading cause of vision impairment in diabetic patients. This study investigates the preventive effects of subconjunctivally applied mesenchymal stem cells (MSCs) pretreated with mammalian target of rapamycin (mTOR) inhibitors on DR.</p><p><strong>Methods: </strong>Thirty-six male Sprague-Dawley rats were used, with diabetes induced by a single intraperitoneal injection of streptozotocin (STZ) at 55 mg/kg. Four groups were established: diabetic control, MSC-treated, everolimus-pretreated MSC-treated (MSC-E), and sirolimus-pretreated MSC-treated (MSC-S). Each treated group received subconjunctival injections of 1 × 106 MSCs in 30 µL phosphate-buffered saline at 3, 5, and 7 weeks post-STZ. Electroretinography (ERG) was performed at 2 and 8 weeks post-STZ. At 11 weeks, cataract formation, uveitis grading, and retinal histology were assessed.</p><p><strong>Results: </strong>mTOR inhibitor-pretreated MSCs significantly prevented the decline in retinal function compared to untreated MSCs and diabetic controls. Everolimus-pretreated MSCs tended to show higher ERG flicker amplitudes than sirolimus-pretreated MSCs, although the difference was not statistically significant. Histologically, both pretreated groups showed preserved thickness in the outer plexiform and nuclear layers, suggesting protection against retinal damage.</p><p><strong>Conclusions: </strong>Subconjunctival application of MSCs pretreated with mTOR inhibitors may help prevent DR progression, with everolimus showing a potential advantage in preserving retinal function.</p><p><strong>Translational relevance: </strong>These findings suggest that mTOR inhibitor-pretreated MSCs could be a viable therapeutic strategy for DR, warranting further clinical trials to confirm efficacy and safety in humans.</p>","PeriodicalId":23322,"journal":{"name":"Translational Vision Science & Technology","volume":"14 9","pages":"19"},"PeriodicalIF":2.6000,"publicationDate":"2025-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12442941/pdf/","citationCount":"0","resultStr":"{\"title\":\"Efficacy of Subconjunctivally Applied Everolimus- and Sirolimus-Pretreated MSCs in Preventing Diabetic Retinopathy.\",\"authors\":\"Ji Seung Jung, Hyo Youn Jo, Jiyi Hwang, Donghee Kim, Myeongjee Kwon, Jungyeon Yong, Haerin Yoon, Hyun Jik Lee, Kyung-Mee Park\",\"doi\":\"10.1167/tvst.14.9.19\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>Diabetic retinopathy (DR) is a leading cause of vision impairment in diabetic patients. This study investigates the preventive effects of subconjunctivally applied mesenchymal stem cells (MSCs) pretreated with mammalian target of rapamycin (mTOR) inhibitors on DR.</p><p><strong>Methods: </strong>Thirty-six male Sprague-Dawley rats were used, with diabetes induced by a single intraperitoneal injection of streptozotocin (STZ) at 55 mg/kg. Four groups were established: diabetic control, MSC-treated, everolimus-pretreated MSC-treated (MSC-E), and sirolimus-pretreated MSC-treated (MSC-S). Each treated group received subconjunctival injections of 1 × 106 MSCs in 30 µL phosphate-buffered saline at 3, 5, and 7 weeks post-STZ. Electroretinography (ERG) was performed at 2 and 8 weeks post-STZ. At 11 weeks, cataract formation, uveitis grading, and retinal histology were assessed.</p><p><strong>Results: </strong>mTOR inhibitor-pretreated MSCs significantly prevented the decline in retinal function compared to untreated MSCs and diabetic controls. 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Histologically, both pretreated groups showed preserved thickness in the outer plexiform and nuclear layers, suggesting protection against retinal damage.</p><p><strong>Conclusions: </strong>Subconjunctival application of MSCs pretreated with mTOR inhibitors may help prevent DR progression, with everolimus showing a potential advantage in preserving retinal function.</p><p><strong>Translational relevance: </strong>These findings suggest that mTOR inhibitor-pretreated MSCs could be a viable therapeutic strategy for DR, warranting further clinical trials to confirm efficacy and safety in humans.</p>\",\"PeriodicalId\":23322,\"journal\":{\"name\":\"Translational Vision Science & Technology\",\"volume\":\"14 9\",\"pages\":\"19\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2025-09-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12442941/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Translational Vision Science & Technology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1167/tvst.14.9.19\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"OPHTHALMOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Translational Vision Science & Technology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1167/tvst.14.9.19","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"OPHTHALMOLOGY","Score":null,"Total":0}
Efficacy of Subconjunctivally Applied Everolimus- and Sirolimus-Pretreated MSCs in Preventing Diabetic Retinopathy.
Purpose: Diabetic retinopathy (DR) is a leading cause of vision impairment in diabetic patients. This study investigates the preventive effects of subconjunctivally applied mesenchymal stem cells (MSCs) pretreated with mammalian target of rapamycin (mTOR) inhibitors on DR.
Methods: Thirty-six male Sprague-Dawley rats were used, with diabetes induced by a single intraperitoneal injection of streptozotocin (STZ) at 55 mg/kg. Four groups were established: diabetic control, MSC-treated, everolimus-pretreated MSC-treated (MSC-E), and sirolimus-pretreated MSC-treated (MSC-S). Each treated group received subconjunctival injections of 1 × 106 MSCs in 30 µL phosphate-buffered saline at 3, 5, and 7 weeks post-STZ. Electroretinography (ERG) was performed at 2 and 8 weeks post-STZ. At 11 weeks, cataract formation, uveitis grading, and retinal histology were assessed.
Results: mTOR inhibitor-pretreated MSCs significantly prevented the decline in retinal function compared to untreated MSCs and diabetic controls. Everolimus-pretreated MSCs tended to show higher ERG flicker amplitudes than sirolimus-pretreated MSCs, although the difference was not statistically significant. Histologically, both pretreated groups showed preserved thickness in the outer plexiform and nuclear layers, suggesting protection against retinal damage.
Conclusions: Subconjunctival application of MSCs pretreated with mTOR inhibitors may help prevent DR progression, with everolimus showing a potential advantage in preserving retinal function.
Translational relevance: These findings suggest that mTOR inhibitor-pretreated MSCs could be a viable therapeutic strategy for DR, warranting further clinical trials to confirm efficacy and safety in humans.
期刊介绍:
Translational Vision Science & Technology (TVST), an official journal of the Association for Research in Vision and Ophthalmology (ARVO), an international organization whose purpose is to advance research worldwide into understanding the visual system and preventing, treating and curing its disorders, is an online, open access, peer-reviewed journal emphasizing multidisciplinary research that bridges the gap between basic research and clinical care. A highly qualified and diverse group of Associate Editors and Editorial Board Members is led by Editor-in-Chief Marco Zarbin, MD, PhD, FARVO.
The journal covers a broad spectrum of work, including but not limited to:
Applications of stem cell technology for regenerative medicine,
Development of new animal models of human diseases,
Tissue bioengineering,
Chemical engineering to improve virus-based gene delivery,
Nanotechnology for drug delivery,
Design and synthesis of artificial extracellular matrices,
Development of a true microsurgical operating environment,
Refining data analysis algorithms to improve in vivo imaging technology,
Results of Phase 1 clinical trials,
Reverse translational ("bedside to bench") research.
TVST seeks manuscripts from scientists and clinicians with diverse backgrounds ranging from basic chemistry to ophthalmic surgery that will advance or change the way we understand and/or treat vision-threatening diseases. TVST encourages the use of color, multimedia, hyperlinks, program code and other digital enhancements.