Name: Preparation of Photo-Oxidized Outer Segment Tips and Fragments
Uploaded: 2023-04-14T14:30:00
Description: Watch this Scientific Journal Video about Preparation of Photo-Oxidized Outer Segment Tips and Fragments at JoVE.com

The video outlines a detailed protocol for preparing and characterizing photo-oxidized outer segments (OS) from retinal cells. It covers the sterilization of slides, treatment with UV light, the resuspension and dilution of OS in culture medium, and assessing lipofuscin accumulation using confocal microscopy.

preparation of photo-oxidized outer segment tips and fragments

القياس الكمي للبلعمة الظهارية الصباغية للشبكية وتراكم ليبوفوسين

The retinal pigment epithelium (RPE) provides critical support for overlying photoreceptors, including the daily uptake and degradation of photoreceptor outer segment tips or fragments (throughout this protocol, the abbreviation OS stands for OS tips or fragments rather than whole outer segments). This daily uptake in the post-mitotic RPE eventually overloads phagolysosomal capacity and leads to the buildup of undigestible, autofluorescent intracellular material, termed lipofuscin. Interestingly, several studies have also demonstrated that RPE lipofuscin can accumulate without OS phagocytosis1,2. Lipofuscin has many components, including cross-linked adducts derived from visual cycle retinoids, and can occupy nearly 20% of RPE cell volume for those over the age of 803.
Whether lipofuscin is toxic has been hotly debated. Stargardt&#39;s disease is an autosomal recessive degeneration of the photoreceptors and RPE in which a mutation in ABCA4 triggers improper processing of visual cycle retinoids contained within photoreceptor outer segments. Improper retinoid processing leads to aberrant cross-linking and formation of bis-retinoid species, including the bis-retinoid N-retinylidene-N-retinylethanolamine (A2E). Studies have demonstrated multiple mechanisms for A2E toxicity4,5. Lipofuscin contributes to fundus autofluorescence signals during clinical imaging, and both Stargardt&#39;s patients and animal models display increased fundus autofluorescence prior to retinal degeneration, suggesting a correlation between lipofuscin levels and toxicity6,7. However, with age, lipofuscin accumulates in all humans without triggering an RPE degeneration. Further, in age-related macular degeneration (AMD), where RPE degeneration occurs only in elderly patients, those with early and intermediate forms of the disease have less fundus autofluorescence signals than age-matched non-diseased humans8. These clinical findings have been verified at the histologic level as well9,10.
Animal models of RPE lipofuscin accumulation have also left some ambiguity about lipofuscin toxicity. The ABCA4 knockout mouse does not display retinal degeneration on a pigmented background, whereas it does on an albino background or when exposed to blue light11,12. Further, the toxicity of lipofuscin derived via ABCA4 knockout likely differs from the more slowly accumulating lipofuscin that occurs with natural aging, as seen in AMD13.
In vitro models of lipofuscin accumulation provide an alternative to studying the effects of lipofuscin accumulation on RPE health. Such models allow for manipulating lipofuscin components, from feeding single retinoid components to feeding OS, and allow study in human rather than animal RPE. In the last couple of decades, multiple methods have been developed to model RPE lipofuscin in culture. Along with other groups, Dr. Boulton&#39;s group fed bovine OS daily for up to three months on passage 4 to 7 human primary RPE cells from donors aged 4 to 85 years old14. Alternatively, inhibition of autophagy has also led to lipofuscin accumulation in passages 3 to 7 primary human RPE cultures15. However, sub-lethal lysosomal inhibition in highly differentiated, passage 1, primary human pre-natal RPE (hfRPE) cultures failed to induce lipofuscin, even with the repeated addition of OS on a daily basis16.
As a more reductionist approach, others have fed single lipofuscin components to cultures, especially the bis-retinoid A2E4,17. Such studies are valuable in that they define potential direct mechanisms of toxicity for individual lipofuscin components, implicating, for example, lysosomal cholesterol and ceramide homeostasis18. At the same time, there is debate about the toxicity of A2E19, and feeding it directly to cells circumvents the typical pathway for lipofuscin accumulation, which involves phagocytosis of photoreceptor OS. In an attempt to deliver all components of lipofuscin to RPE cultures, Boulton and Marshall purified lipofuscin from human eyes and fed this to passage 4 to 7 human primary RPE cultures derived from both fetal and elderly human donors20. While innovative, this method represents a limited lipofuscin source for repeated experiments.
While repeated feedings of OS to RPE cultures produce lipofuscin in many systems, it fails to do so in highly differentiated primary RPE cultures16. Photo-oxidizing OS induces cross-linking reactions like bis-retinoid formation that naturally occurs during lipofuscin formation in vivo. This can accelerate lipofuscin-like granule formation in RPE culture systems, even those that are highly differentiated and resistant to lipofuscin accumulation16. Here, a method to induce lipofuscin-like granule accumulation in highly differentiated hfRPE and human iPSC-RPE is introduced, modified from Wihlmark&#39;s published protocol21. This method has the advantage of inducing lipofuscin-like granules employing the same source (photoreceptor OS) and pathway (phagolysosomal OS uptake) as occurs for lipofuscinogenesis in vivo. Further, it is done on human RPE cultures that are highly differentiated and validated in multiple studies to replicate human RPE in vivo22,23,24. These lipofuscin-like granules are termed undigestible autofluorescent material (UAM), and provide data and discussion in this protocol comparing UAM to in vivo lipofuscin. Along with methods for building and evaluating UAM-laden cultures in highly differentiated human RPE, an updated method to assess RPE OS phagocytosis is also introduced. Multiple excellent pulse-chase methods for quantifying OS phagocytosis have been introduced, including Western blotting, immunocytochemistry, and FACS25,26,27. However, early in the OS pulse-chase, conditions that lead to poor OS uptake can be conflated with conditions that promote rapid degradation of internalized OS. The method presented here measures the total amount of introduced OS that is fully consumed/degraded by the RPE (&#34;Total Consumptive Capacity&#34;), helping eliminate this ambiguity. It is anticipated that insights about lipofuscin toxicity utilizing these protocols, including effects on OS phagocytosis rates utilizing the &#34;Total Consumptive Capacity&#34; method, will be used to shed light on the toxicity of lipofuscin in vivo.

تسليط الضوء على المؤلف: تحسين نماذج ليبوفوسين والقياس الكمي لقدرة البلعمة في الجزء الخارجي في الثقافات الظهارية الصبغية الشبكية البشرية شديدة الاستقطاب  

تحسين نماذج ليبوفوسين والقياس الكمي لقدرة البلعمة في الجزء الخارجي في الثقافات الظهارية الصبغية للشبكية البشرية شديدة الاستقطاب

While lipofuscin universally accumulates in the RPE with aging, discerning its toxicity has been difficult. Here, we develop protocols that allow us to develop lipofuscin-like accumulation in highly polarized and mature RPE cultures to help discern lipofuscin's effects on RPE physiology. Studying lipofuscin toxicity in humans is confounded by the fact that lipofuscin decreases as the RPE dies.Animal models of lipofuscin toxicity have had widely disparate results. We have carefully created in vitro models of lipofuscin-like material accumulation to facilitate the study of lipofuscin toxicity. The key to the success of our models is maintaining highly differentiated cultures while inducing lipofuscin genesis via the same process that triggers lipofuscin in vivo, namely phagocytosis of photoreceptor outer segments.Our in vitro protocol is unique in that lipofuscin-like material accumulates in RPE cultures that are highly differentiated to faithfully mimic RPE in vivo. In these circumstances, we found that RPE culture are highly resistant to the lipofuscin accumulation and to toxic effect from lipofuscin. Additionally, in the process of assaying for phenotypes induced by lipofuscin-like accumulation in our RPE cultures, we created a new type of phagocytosis assay called total consumptive capacity.This assay allows us to determine the entire capacity of the RPE to phagocytose outer segments while avoiding some of the confounding interpretations that come with classical pulse-chase phagocytosis assays. We are excited to utilize this model of lipofuscin-like material accumulation to better understand what RPE stressors may take normally inert lipofuscin into a more pathological role in RPE cell deaths.

Watch this Scientific Journal Video about Preparation of Photo-Oxidized Outer Segment Tips and Fragments at JoVE.com

Preparation of Photo-Oxidized Outer Segment Tips and Fragments  

تحضير أطراف وشظايا الجزء الخارجي المؤكسد ضوئيا

ابدأ بتعقيم الشرائح المطلية بالبولي تترافلوروإيثيلين ، أو الشرائح المطلية ب PTFE عن طريق غمرها في 70٪ من الإيثانول لمدة 10 دقائق في خزانة السلامة الحيوية. اترك الشرائح تجف في الهواء في طبق زراعة خلية معقم بحجم 100 ملم. ضع كل شريحة في 1 طبق جديد لزراعة الخلايا 100 ملم وأضف 200 ميكرولتر من وسط زراعة الخلايا المحتوي على المصل في كل مستطيل.ثم ضع ضوء الأشعة فوق البنفسجية المحمول باليد 254 نانومتر على طبق زراعة الخلايا 100 ملم مع مواجهة المصباح مباشرة للشريحة لمدة 20 دقيقة. قم بإذابة القسامات المجمدة للأجزاء الخارجية ، أو OS ، في حمام مائي بدرجة حرارة 37 درجة مئوية. ثم قم بتدوير نظام التشغيل عند 2،400G لمدة خمس دقائق في درجة حرارة الغرفة.قم على الفور بشفط المادة الطافية في خزانة السلامة البيولوجية باستخدام ماصة وأعد تعليق نظام التشغيل في PBS. الآن ، قم باستنشاق الوسيط من الشرائح ووضع ما يصل إلى 500 ميكرولتر من 2 × 10 إلى نظام التشغيل الثامن لكل مليلتر حل PBS من 2 × 10 إلى 8th OS لكل مليلتر حل PBS على كل مستطيل شريحة. ضع ضوء الأشعة فوق البنفسجية المحمول باليد 254 نانومتر فوق طبق زراعة الخلايا بحيث تواجه اللمبة نظام التشغيل مباشرة لمدة 40 دقيقة.اجمع محلول OS-PBS في أنبوب سعة 1.5 ملليلتر. اغسل مستطيل الشريحة المطلية ب 200 إلى 500 ميكرولتر من PBS واجمع كل غسلة في أنبوب الطرد المركزي الدقيق. ثم قم بتدوير حل OS-PBS عند 2،400G لمدة خمس دقائق في درجة حرارة الغرفة.نضح PBS في خزانة السلامة البيولوجية باستخدام أنبوب وإعادة تعليق الحبيبات في 500 ميكرولتر من الوسط القياسي لاستخدامها في ظهارة صبغة الشبكية ، أو مزارع RPE. ضع 10 ميكرولتر من التعليق في أنبوب طرد مركزي جديد. تمييع 50 إلى 100 مرة مع المزيد من وسط زراعة الخلايا ، وحساب نظام التشغيل مع مقياس الدم.قم بتخفيف نظام التشغيل المؤكسد بالصور ، أو تعليق OxOS ، عند تركيز 5.6 × 10 إلى نظام التشغيل السابع لكل مليلتر في وسيط RPE قياسي. أضف روابط سد البلعمة ، والتي تسهل امتصاص نظام التشغيل وتراكم الليبوفوسين. ثم قم بقسمة OxOS في مخزون يستخدم مرة واحدة وتجمد مفاجئ في النيتروجين السائل.قم بإذابة حصص OxOS عن طريق تخفيف القسمة المجمدة في 45 ميكرولتر من وسائط زراعة الخلايا قبل إضافتها إلى عمليات نقل RPE للحث على تراكم الليبوفوسين. ثم قم بتوصيف نظام التشغيل المؤكسد عن طريق قياس طيف انبعاث OxOS باستخدام مسح Lambda على مجهر متحد البؤر. أظهر التصوير البؤري أن نظام التشغيل المعالج قد زاد من التألق الذاتي مقارنة بنظام التشغيل غير المعالج.

Research

JoVE Journal

Biology

Preparation of Photo-Oxidized Outer Segment Tips and Fragments

Improved Lipofuscin Models and Quantification of Outer Segment Phagocytosis Capacity in Highly Polarized Human Retinal Pigment Epithelial Cultures

The daily phagocytosis of photoreceptor outer segments by the retinal pigment epithelium (RPE) contributes to the accumulation of an intracellular aging ...