この研究室で緑内障の研究は、アメリカの健康アシスタント財団からの国立緑内障の研究によってサポートされています。

<ol><li>ピペットプラーを使用してガラスピペットを準備し、1ミリリットル注射器に接続し、パラフィルムで接続をシール。ピペットの先端に溶液2 mlを撤回し、注射の準備をする。 </li><li>ケタミン（80mg/kg）とキシラジン（8mg/kg）（2:1体積比）の腹腔内注射によってラットをAnaesthetize。 </li><li>硝子体内注射の前に局所麻酔薬としてラットの眼に0.5％alcaineの一滴を適用します。 </li><li>ラットを配置し、眼の優れた鼻の領域を公開する。 </li><li>優れた鼻強膜はパープラナのレベルでの穿刺に30ゲージの針を使用してください。眼の筋肉や血管に触れないようにしてください。 </li><li>後房からの穿刺孔から硝子体の少量を取り除くために眼球穏やかな圧力を与える。 </li><li>硝子体内に強膜を介して45 °の角度で穿刺孔を介してガラスピペットの先端を挿入します。後チャンバーに溶液2 mlを注入し、数秒程度の場所に保管して、そっと針を取り除く。レンズや眼内血管に触れないようにしてください。 </li><li>硝子体内注射後、感染を防ぐために、ラットの目に点眼Tobrexの軟膏を塗る。 </li></ol>

<ol>
	<li>Chiu, K., Lam, T. T., Ying Ku, W. W., Caprioli, J., Kwong Kwong, J. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Calpain+and+N-methyl-d-aspartate+(NMDA)-induced+excitotoxicity+in+rat+retinas.">Calpain and N-methyl-d-aspartate (NMDA)-induced excitotoxicity in rat retinas.</a> Brain Research. 1046, 207-215 (2005).</li><li>Fisher, D., Pavlidis, M., Thanos, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cataractogenic+lens+injury+prevents+traumatic+ganglion+cell+death+and+promotes+axonal+regeneration+both+in+vivo+and+in+culture.">Cataractogenic lens injury prevents traumatic ganglion cell death and promotes axonal regeneration both in vivo and in culture.</a> Investigative Ophthalmology &amp; Visual Science. 41, 3943-3954 (2000).</li><li>Ji, J. -. Z., Elyaman, W., Yip, H. K., Lee, V. W. H., Yick, L. -. W., Hugon, J., So, K. -. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=CNTF+promotes+survival+of+retinal+ganglion+cells+after+induction+of+ocular+hypertension+in+rats:+the+possible+involvement+of+STAT3+pathway.">CNTF promotes survival of retinal ganglion cells after induction of ocular hypertension in rats: the possible involvement of STAT3 pathway.</a> European Journal of Neuroscience. 19, 265-272 (2004).</li><li>Lam, T. T., Abler, A. S., Kwong, J. M. K., Tso, M. O. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=N-Methyl-D-Aspartate+(NMDA)-Induced+Apoptosis+in+Rat+Retina.">N-Methyl-D-Aspartate (NMDA)-Induced Apoptosis in Rat Retina.</a> Investigative Ophthalmology &amp; Visual Science. 40, 2391-2397 (1999).</li></ol>

動物は、ビジョンと眼科文で、香港の大学の教育と研究に生きている動物の使用（CULATR）に委員会で承認された研究における動物の使用と研究のための協会のためのプロトコルに従って処理されていました眼科とビジョン研究における動物の使用。

良い硝子注射は、動物モデルだけでなく、直接眼の治療を確立するのに便利です。最初に、注射部位は、網膜の構造を破壊するではありません。第二に、出血、感染のリスクを減らすために避けるべきである。第三に、レンズは、外傷性白内障を避けるために触れられすべきである。最も重要なのは、通常の眼の構造の中断を減らすことです。

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		<div>
		<table border="1">
		<thead>
		<tr>
		<th>Material Name</th>
		<th>Type</th>
		<th>Company</th>
		<th>Catalogue Number</th>
		<th>Comment</th>
		</tr>
		</thead>
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<tr>
<td>Operating Microscope </td>
<td>&nbsp;</td>
<td>Olympus</td>
<td>OME</td>
<td>&nbsp;</td>
<tr>
<td>Glass Pipettes </td>
<td>&nbsp;</td>
<td>World Precision Instruments, Inc.</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<tr>
<td>Pipette Puller </td>
<td>&nbsp;</td>
<td>David Kopf Instruments</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<tr>
<td>1ml syringes</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>single use</td>
</tr>
<tr>
<td>30G needles</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>single use</td>
</tr>
<tr>
<td>Ketamine</td>
<td>&nbsp;</td>
<td>Aldasan</td>
<td>&nbsp;</td>
<td>anesthetic</td>
</tr>
<tr>
<td>Xylazine</td>
<td>&nbsp;</td>
<td>Aldasan</td>
<td>&nbsp;</td>
<td>anesthetic</td>
</tr>
<tr>
<td>Alcaine</td>
<td>&nbsp;</td>
<td>Alcon-Couvreur</td>
<td>&nbsp;</td>
<td>0.5% proparacaine hydrochloride</td>
</tr>
<tr>
<td>Tobrex</td>
<td>&nbsp;</td>
<td>Alcon-Couvreur</td>
<td>&nbsp;</td>
<td>ointment, 3% tobramyxin.</td>
</tr>		</tbody>
		</table>
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intravitreous injection for establishing ocular diseases model

硝子体内注射は、視覚科学の研究に広く使用されている技術です。それは、眼疾患、または局所治療の直接的な応用として動物モデルを確立するために使用することができます。このビデオでは、硝子体内注射の手順を完了するためのシンプルで安価なツールを使用する方法を紹介します。 、代わりにhemiltonシリンジの、1 mlの注射器の使用が使用されます。実用的な完璧なヒントをガラスピペットを用いて適切な注射針を作る方法のヒント、そしてどのように簡単にしっかりと一緒にガラスピペットと注射針を接続するためには、与えられている。 良い硝子の注入を行うために、観察される3つの側面があります：1）注射部位は、網膜の構造を破壊しないでください。2）出血は、感染のリスクを減らすために避けるべきである、3）レンズは、外傷性白内障を避けるために触れられすべきである。簡単に言えば、最も重要なポイントは、通常の眼の構造の中断を減らすことです。網膜の中断を避けるために、ラットの眼の優れた鼻の領域が選択されまし​​た。また、針の穿刺のポイントは、ラットの眼の角膜輪部地域から約1.5 mmであるパー​​平面、にあった。硝子体の少量を穏やかに注入する前に眼圧を軽減するために穿刺孔から押し出される。 45 °の射出角と、それはこのように、レンチキュラー要因から関連する合併症と影響を避け、ラッ​​トの眼の外傷性白内障が発生する可能性が低くなります。この操作では、結膜や眼筋のないカット、出血はありませんでした。迅速で軽傷で、成功した硝子体内注入は数分で行うことができます。 注入この特定のプロトコルに記載されている設定は、硝子体内注射のための固有のものです。しかし、ここで紹介する方法および材料はまた、脳、脊髄または小型哺乳類の他の臓器への薬物送達における他の注射の手順については、使用することができます。

Watch this Scientific Journal Video about Intravitreous Injection for Establishing Ocular Diseases Model at JoVE.com

Intravitreous Injection for Establishing Ocular Diseases Model

硝子体内注射、眼の疾患のためのまたは局所治療の直接的な応用として、視覚科学の研究に広く使用されている技術です。このビデオでは、ガラスピペットで1ミリリットル注射器を使用して硝子体内注射のためのプロトコルを示した。大量出血し、レンズの損傷を避けることについての有用なヒントが与えられている。

眼疾患モデルを確立するための硝子体内注射

Intravitreous injection is a widely used technique in visual sciences research. It can be used to establish animal models with ocular diseases or as ...

intravitreous-injection-for-establishing-ocular-diseases-model

Research

JoVE Journal

Biology

36.5K ビュー.  The University of Hong Kong - HKU. 硝子体内注射、眼の疾患のためのまたは局所治療の直接的な応用として、視覚科学の研究に広く使用されている技術です。このビデオでは、ガラスピペットで1ミリリットル注射器を使用して硝子体内注射のためのプロトコルを示した。大量出血し、レンズの損傷を避けることについての有用なヒントが与えられている。

ビデオ: Intravitreous Injection for Establishing Ocular Diseases Model

Laser-Induced Chronic Ocular Hypertension Model on SD Rats

Glaucoma is one of the major causes of blindness in the world. Elevated intraocular pressure is a major risk factor. Laser photocoagulation induced ocular hypertension is one of the well established animal models. This video demonstrates how to induce ocular hypertension by Argon laser photocoagulation in rat.

Glaucoma is one of the major causes of blindness in the world. Elevated intraocular pressure is a major risk factor. Laser photocoagulation induced ocular hypertension is one of the well established animal models. This video demonstrates how to induce ocular hypertension by Argon laser photocoagulation in rat.

SDラットにおけるレーザー誘起慢性高眼圧症モデル

Glaucoma is one of the major causes of blindness in the world. Elevated intraocular pressure is a major risk factor. Laser photocoagulation induced ocular ...

生物学

Interview: Protein Folding and Studies of Neurodegenerative Diseases

In this interview, Dr. Lindquist describes relationships between protein folding, prion diseases and neurodegenerative disorders. The problem of the protein folding is at the core of the modern biology. In addition to their traditional biochemical functions, proteins can mediate transfer of biological information and therefore can be considered a genetic material. This recently discovered function of proteins has important implications for studies of human disorders. Dr. Lindquist also describes current experimental approaches to investigate the mechanism of neurodegenerative diseases based on genetic studies in model organisms.

In this interview, Dr. Lindquist describes relationships between protein folding, prion diseases and neurodegenerative disorders. The problem of the protein folding is at the core of the modern biology. In addition to their traditional biochemical functions, proteins can mediate transfer of biological information and therefore can be considered a genetic material. This recently discovered function of proteins has important implications for studies of human disorders. Dr. Lindquist also describes current experimental approaches to investigate the mechanism of neurodegenerative diseases based on genetic studies in model organisms.

インタビュー：タンパク質フォールディングと神経変性疾患の研究

In this interview, Dr. Lindquist describes relationships between protein folding, prion diseases and neurodegenerative disorders. The problem of the ...

Zebrafish Brain Ventricle Injection

Proper brain ventricle formation during embryonic brain development is required for normal brain function.  Brain ventricles are the highly conserved cavities within the brain that are filled with cerebrospinal fluid.  In zebrafish, after neural tube formation, the neuroepithelium undergoes a series of constrictions and folds while it fills with fluid resulting in brain ventricle formation.  In order to understand the process of ventricle formation, and the neuroepithelial shape changes that occur at the same time, we needed a way to visualize the ventricle space in comparison to the brain tissue.  However, the nature of transparent zebrafish embryos makes it difficult to differentiate the tissue from the ventricle space.  Therefore, we developed a brain ventricle injection technique where the ventricle space is filled with a fluorescent dye and imaged by brightfield and fluorescent microscopy.  The brightfield and the fluorescent images are then processed and superimposed in Photoshop.  This technique allows for visualization of the ventricle space with the fluorescent dye, in comparison to the shape of the neuroepithelium in the brightfield image.  Brain ventricle injection in zebrafish can be employed from 18 hours post fertilization through early larval stages.  We have used this technique extensively in our studies of brain ventricle formation and morphogenesis as well as in characterizing brain morphogenesis mutants (1-3).

After neural tube formation, the neuroepithelium constricts and folds while the tube fills with embryonic cerebrospinal fluid (eCSF) to form the embryonic brain ventricles. We developed this ventricle injection technique to better visualize the fluid filled space in contrast to the neuroepithelial shape in a live embryo.

ゼブラフィッシュの脳室注入

Proper brain ventricle formation during embryonic brain development is required for normal brain function.  Brain ventricles are the highly conserved ...

Sample Preparation for Mass-spectrometry-based Proteomics Analysis of Ocular Microvessels

The use of isolated ocular blood vessels in vitro to decipher the pathophysiological state of the eye using advanced technological approaches has greatly expanded our understanding of certain diseases. Mass spectrometry (MS)-based proteomics has emerged as a powerful tool to unravel alterations in the molecular mechanisms and protein signaling pathways in the vascular beds in health and disease. However, sample preparation steps prior to MS analyses are crucial to obtain reproducible results and in-depth elucidation of the complex proteome. This is particularly important for preparation of ocular microvessels, where the amount of sample available for analyses is often limited and thus, poses a challenge for optimum protein extraction. This article endeavors to provide an efficient, rapid and robust protocol for sample preparation from an exemplary retrobulbar ocular vascular bed employing the porcine short posterior ciliary arteries. The present method focuses on protein extraction procedures from both the supernatant and pellet of the sample following homogenization, sample cleaning with centrifugal filter devices prior to one-dimensional gel electrophoresis and peptide purification steps for label-free quantification in a liquid chromatography-electrospray ionization-linear ion trap-Orbitrap MS system. Although this method has been developed specifically for proteomics analyses of ocular microvessels, we have also provided convincing evidence that it can also be readily employed for other tissue-based samples.

Proteome characterization of ocular microvascular beds is pivotal for in-depth understanding of many ocular pathologies in humans. This study demonstrates an effective, rapid, and robust method for protein extraction and sample preparation from small blood vessels employing the porcine short posterior ciliary arteries as model vessels for mass-spectrometry-based proteomics analyses.

眼微小循環の質量分析法を用いたプロテオミクス解析の前処理

The use of isolated ocular blood vessels in vitro to decipher the pathophysiological state of the eye using advanced technological approaches has greatly ...

Mass Spectrometry Analysis to Identify Ubiquitylation of EYFP-tagged CENP-A (EYFP-CENP-A)

Studying the structure and the dynamics of kinetochores and centromeres is important in understanding chromosomal instability (CIN) and cancer progression. How the chromosomal location and function of a centromere (i.e., centromere identity) are determined and participate in accurate chromosome segregation is a fundamental question. CENP-A is proposed to be the non-DNA indicator (epigenetic mark) of centromere identity, and CENP-A ubiquitylation is required for CENP-A deposition at the centromere, inherited through dimerization between cell division, and indispensable to cell viability.
Here we describe mass spectrometry analysis to identify ubiquitylation of EYFP-CENP-A K124R mutant suggesting that ubiquitylation at a different lysine is induced because of the EYFP tagging in the CENP-A K124R mutant protein. Lysine 306 (K306) ubiquitylation in EYFP-CENP-A K124R was successfully identified, which corresponds to lysine 56 (K56) in CENP-A through mass spectrometry analysis. A caveat is discussed in the use of GFP/EYFP or the tagging of high molecular weight protein as a tool to analyze the function of a protein. Current technical limit is also discussed for the detection of ubiquitylated bands, identification of site-specific ubiquitylation(s), and visualization of ubiquitylation in living cells or a specific single cell during the whole cell cycle.
The method of mass spectrometry analysis presented here can be applied to human CENP-A protein with different tags and other centromere-kinetochore proteins. These combinatory methods consisting of several assays/analyses could be recommended for researchers who are interested in identifying functional roles of ubiquitylation.

Mass Spectrometry Analysis to Identify Ubiquitylation of EYFP-tagged CENP-A EYFP-CENP-A

CENP-A ubiquitylation is an important requirement for CENP-A deposition at the centromere, inherited through dimerization between cell division, and indispensable to cell viability. Here we describe mass spectrometry analysis to identify ubiquitylation of EYFP-tagged CENP-A (EYFP-CENP-A) protein.

EYFP タグ付き CENP-A (EYFP-CENP-A) のユビキタス性を同定するための質量分析分析

Studying the structure and the dynamics of kinetochores and centromeres is important in understanding chromosomal instability (CIN) and cancer ...

Modeling Age-Associated Neurodegenerative Diseases in Caenorhabditis elegans

Battling human neurodegenerative pathologies and managing their pervasive socioeconomic impact is becoming a global priority. Notwithstanding their detrimental effects on the human life quality and the healthcare system, the majority of human neurodegenerative disorders still remain incurable and non-preventable. Therefore, the development of novel therapeutic interventions against such maladies is becoming a pressing urgency. Age-associated deterioration of neuronal circuits and function is evolutionarily conserved in organisms as diverse as the lowly worm Caenorhabditis elegans and humans, signifying similarities in the underlying cellular and molecular mechanisms. C. elegans is a highly malleable genetic model, which offers a well-characterized nervous system, body transparency and a diverse repertoire of genetic and imaging techniques to assess neuronal activity and quality control during ageing. Here, we introduce and describe methodologies utilizing some versatile nematode models, including hyperactivated ion channel-induced necrosis (e.g., deg-3(d) and mec-4(d)) and protein aggregate (e.g., &#945;-syunclein and poly-glutamate)-induced neurotoxicity, to monitor and dissect the cellular and molecular underpinnings of age-related neuronal breakdown. A combination of these animal neurodegeneration models, together with genetic and pharmacological screens for cell death modulators will lead to an unprecedented understanding of age-related breakdown of neuronal function and will provide critical insights with broad relevance to human health and quality of life.

Modeling Age-Associated Neurodegenerative Diseases in Caenorhabditis elegans

Here, we introduce and describe widely accessible methodologies utilizing some versatile nematode models, including hyperactivated ion channel-induced necrosis and protein aggregate-induced neurotoxicity, to monitor and dissect the cellular and molecular underpinnings of age-associated neurodegenerative diseases.

カエノハブディティス・エレガンスにおける年齢関連神経変性疾患のモデル化

Battling human neurodegenerative pathologies and managing their pervasive socioeconomic impact is becoming a global priority. Notwithstanding their ...

An Ex Vivo Choroid Sprouting Assay of Ocular Microvascular Angiogenesis

Pathological choroidal angiogenesis, a salient feature of age-related macular degeneration, leads to vision impairment and blindness. Endothelial cell (EC) proliferation assays using human retinal microvascular endothelial cells (HRMECs) or isolated primary retinal ECs are widely used in vitro models to study retinal angiogenesis. However, isolating pure murine retinal endothelial cells is technically challenging and retinal ECs may have different proliferation responses than choroidal endothelial cells and different cell/cell interactions. A highly reproducible ex vivo choroidal sprouting assay as a model of choroidal microvascular proliferation was developed. This model includes the interaction between choroid vasculature (EC, macrophages, pericytes) and retinal pigment epithelium (RPE). Mouse RPE/choroid/scleral explants are isolated and incubated in growth-factor-reduced basal membrane extract (BME) (day 0). Medium is changed every other day and choroid sprouting is quantified at day 6. The images of individual choroid explant are taken with an inverted phase microscope and the sprouting area is quantified using a semi-automated macro plug-in to the ImageJ software developed in this lab. This reproducible ex vivo choroidal sprouting assay can be used to assess compounds for potential treatment and for microvascular disease research to assess pathways involved in choroidal micro vessel proliferation using wild type and genetically modified mouse tissue.

This protocol presents choroid sprouting assay, an ex vivo model of microvascular proliferation. This assay can be used to assess pathways involved in proliferating choroidal micro vessels and assess drug treatments using wild type and genetically modified mouse tissue.

眼小血管血管新生のエキビボロイド発芽アッセイ

Pathological choroidal angiogenesis, a salient feature of age-related macular degeneration, leads to vision impairment and blindness. Endothelial cell ...

Establishing Human Lung Organoids and Proximal Differentiation to Generate Mature Airway Organoids

The lack of a robust in vitro model of the human respiratory epithelium hinders the understanding of the biology and pathology of the respiratory system. We describe a defined protocol to derive human lung organoids from adult stem cells in the lung tissue and induce proximal differentiation to generate mature airway organoids. The lung organoids are then consecutively expanded for over 1 year with high stability, while the differentiated airway organoids are used to morphologically and functionally simulate human airway epithelium to a near-physiological level. Thus, we establish a robust organoid model of the human airway epithelium. The long-term expansion of lung organoids and differentiated airway organoids generates a stable and renewable source, enabling scientists to reconstruct and expand the human airway epithelial cells in culture dishes. The human lung organoid system provides a unique and physiologically active in vitro model for various applications, including studying virus-host interaction, drug testing, and disease modeling.

The protocol presents a method to derive human lung organoids from primary lung tissues, expand the lung organoids and induce proximal differentiation to generate 3D and 2D airway organoids that faithfully phenocopy the human airway epithelium.

ヒト肺オルガノイドの確立と近位分化による成熟気道オルガノイドの生成

The lack of a robust in vitro model of the human respiratory epithelium hinders the understanding of the biology and pathology of the respiratory system. ...

Efficient and Consistent Generation of Retinal Pigment Epithelium/Choroid Flatmounts from Human Eyes for Histological Analysis

The retinal pigment epithelium (RPE) and retina are functionally and structurally connected tissues that work together to regulate light perception and vision. Proteins on the RPE apical surface are tightly associated with proteins on the photoreceptor outer segment surface, making it difficult to consistently separate the RPE from the photoreceptors/retina. We developed a method to efficiently separate the retina from the RPE of human eyes to generate complete RPE/choroid and retina flatmounts for separate cellular analysis of the photoreceptors and RPE cells. An intravitreal injection of a high-osmolarity solution of D-mannitol, a sugar not transported by the RPE, induced the separation of the RPE and retina across the entire posterior chamber without causing damage to the RPE cell junctions. No RPE patches were observed attached to the retina. Phalloidin labeling of actin showed RPE shape preservation and allowed morphometric analysis of the entire epithelium. An artificial intelligence (AI)-based software was developed to accurately recognize and segment the RPE cell borders and quantify 30 different shape metrics. This dissection method is highly reproducible and can be easily extended to other animal models.

We describe a method to efficiently separate retinal pigment epithelium (RPE) from the retina in human eyes and generate whole RPE/choroid flatmounts for histological and morphometric analyses of the RPE.

組織学的分析のためのヒトの眼からの網膜色素上皮/脈絡膜フラットマウントの効率的かつ一貫した生成

The retinal pigment epithelium (RPE) and retina are functionally and structurally connected tissues that work together to regulate light perception and ...

Establishing a Diaphyseal Femur Fracture Model in Mice

Bones have a significant regenerative capacity. However, fracture healing is a complex process, and depending on the severity of the lesions and the age and overall health status of the patient, failures can occur, leading to delayed union or nonunion. Due to the increasing number of fractures resulting from high-energy trauma and aging, the development of innovative therapeutic strategies to improve bone repair based on the combination of skeletal/mesenchymal stem/stromal cells and biomimetic biomaterials is urgently needed. To this end, the use of reliable animal models is fundamental to better understanding the key cellular and molecular mechanisms that determine the healing outcomes. Of all the models, the mouse is the preferred research model because it offers a wide variety of transgenic strains and reagents for experimental analysis. However, the establishment of fractures in mice may be technically challenging due to their small size. Therefore, this article aims to demonstrate the procedures for the surgical establishment of a diaphyseal femur fracture in mice, which is stabilized with an intramedullary wire and resembles the most common bone repair process, through cartilaginous callus formation.

This protocol describes a surgical procedure for the establishment of a diaphyseal fracture in the femur of mice, which is stabilized with an intramedullary wire, for fracture healing studies.

マウスにおける骨幹大腿骨骨折モデルの確立

Bones have a significant regenerative capacity. However, fracture healing is a complex process, and depending on the severity of the lesions and the age ...