בהכרת תודה אנו מכירים את התמיכה מענק Pilot מקרן המחקר סטנפורד ילדים ו K08DK087895-01 מ NIDDK.

1. שלפוחית ​​השתן עכבר וול Injection בחירת זן העכבר, גיל, מין מוכתב על ידי הצרכים ניסיוני. אנו משתמשים בעכברים בין 8 ל 12 שבועות של גיל, שכן זהו חלון של בגרות החיסונית לקראת ההזדקנות. כקו מנחה כללי, עכברים צריכים להגיע לפחות שבוע לפני מניפולציה ניסויית על מנת למנוע מתח המושרה גורמים סותרים. <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> נקו את משטח השולחן כירורגית עם מים וסבון. </li><li style=";text-align:right;direction:rtl"> נגבו את משטח השולחן כירורגית במשיכות Cide או מגבונים חיטוי. </li><li style=";text-align:right;direction:rtl"> החיטוי מכשירי ניתוח נקי לפני השימוש בניתוח. </li><li style=";text-align:right;direction:rtl"> בנוסף, לחטא כלי ניתוח עם מעקר חרוז חם מיד לפני השימוש, וכן בין בעלי חיים במהלך הניתוח. </li><li style=";text-align:right;direction:rtl"> ניקוי מזרקים 100 μL המילטון 29 או 30 מד (1 / 2 אינץ ארוך) מחטים על ידי שאיפה חוזרות ההזרקה עם אלכוהול מוחלט לפני השימוש הראשון בסוף ההליך הכירורגי הסופי. </li><li style=";text-align:right;direction:rtl"> לרחוץ ולשטוף מזרקים המילטון עם מעוקרים פוספט שנאגרו מלוחים בין כל חיה. </li><li style=";text-align:right;direction:rtl"> הרדימי עכברים ידי הצבתם בחדר אינדוקציה isoflurane, עם להגדיר את isoflurane בין 2-5%. </li><li style=";text-align:right;direction:rtl"> לאחר הרדמה כללית מושגת, להסיר את העכבר מהאולם ובמקום במצב שכיבה עם כרית חמה מתחת מנת לשמור על חום גוף תקין. </li><li style=";text-align:right;direction:rtl"> השג הרדמה תחזוקה ידי הצבת חוטם של החיה בנחיר המכיל לאדות isoflurane (טיטרציה של 1-3% על פי הצורך לשמור על הרדמה המתאים). </li><li style=";text-align:right;direction:rtl"> לגלח את עור הבטן עם קוצץ. </li><li style=";text-align:right;direction:rtl"> השתמש לעטוף חד פעמיות, כירורגי סטרילי כדי לכסות את פי הטבעת על מנת למנוע זיהום צואתי במהלך הניתוח. </li><li style=";text-align:right;direction:rtl"> השתמש לעטוף שנייה חד פעמיות, כירורגי סטרילי כדי לכסות את שדה הניתוח (הבטן התחתונה). </li><li style=";text-align:right;direction:rtl"> הכיני את הבטן עם שלוש חתיכות של גזה בבטאדין ספוג. חזור על שלב זה שלוש פעמים. </li><li style=";text-align:right;direction:rtl"> באמצעות מיקרוסקופ לנתח עבור ההגדלה, לעשות חתך בבטן התחתונה קו האמצע עם מספריים. </li><li style=";text-align:right;direction:rtl"> לחשוף את שלפוחית ​​השתן. </li><li style=";text-align:right;direction:rtl"> אם השלפוחית ​​מלאה, חלקית לשחרר אותו על ידי לחץ כלפי מטה בעדינות על הכיפה. </li><li style=";text-align:right;direction:rtl"> להזריק את הפתרון המדגם (עד 50 μL), באמצעות מחט 29 או 30 מד מזרק, בקיר של הכיפה שלפוחית ​​השתן (הזרקה עירונית) עם שיפוע של המחט פונה כלפי מעלה. </li><li style=";text-align:right;direction:rtl"> דחוף את הבוכנה של המזרק להזריק את הפתרון מדגם לתוך הקיר שלפוחית ​​השתן. בועה היטב מקומי אינדיקציה זריקה מוצלחת של התאים בדופן שלפוחית ​​השתן. </li><li style=";text-align:right;direction:rtl"> הסר את המזרק, לסגור את החתך עם קליפים הפצע ולאפשר העכבר כדי להתאושש על כרית חימום. </li></ol> 2. נציג תוצאות: בועה היטב מקומי שאינו נוזל דליפה ונשאר יציב בגודל אינדיקציה זריקה מוצלחת של התאים בדופן שלפוחית ​​השתן (איור 1). ניתוח היסטולוגית ניתן לבצע כדי לאשר את קיומו של התאים מוזרקים בדופן שלפוחית ​​השתן. <img src="/files/ftp_upload/2523/2523fig1.jpg" alt="איור 1"/> באיור 1. דוגמה זריקה מוצלחת קיר שלפוחית ​​השתן באמצעות דיו הודו להמחשה. <img src="/files/ftp_upload/2523/2523fig2.jpg" alt="איור 2"/> איור 2. סכמטי של הפרוצדורות.

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שלפוחית ​​השתן עכבר הזרקת הקיר מאפשר להשתלה של תאים ספציפיים לאזורים מוגדרים של קיר שלפוחית ​​השתן. טכניקה זו יש יישומים רחב עבור מודלים העכבר של סרטן שלפוחית ​​השתן, שריר חלק, ביולוגיה של התא גזע. על פי ההגדרה, שלפוחית ​​השתן העכבר מאפשר הזרקה קיר המבוא של סרטן ש...

<table border="1" style=";text-align:right;direction:rtl"><tbody><tr><td> שם מגיב </td><td> חברה </td><td> מספר קטלוגי </td></tr><tr><td> Isoflurane (Aerrane) </td><td> בקסטר </td><td> NDC 10019-773-60 </td></tr><tr><td> 29 או 30 מד מחטים </td><td> המילטון </td><td> 7803-06 או 7803-07 </td></tr><tr><td> 100 microliter מזרק </td><td> המילטון </td><td> 7656-01 </td></tr></tbody></table>

mouse bladder wall injection

שלפוחית ​​השתן עכבר הזרקת בקיר היא טכניקה יעילה כדי ללמוד orthotopically תופעות שלפוחית ​​השתן, כולל בתאי גזע, שריר חלק, ביולוגיה סרטן. לפני שמתחילים זריקות, באזור הניתוח יש לנקות עם מים וסבון אנטיספטי פתרון. ציוד כירורגי יש לעקר לפני השימוש לבין כל חיה. עכבר כל מושם תחת הרדמה נשאפים isoflurane (2-5% לזירוז,% 1-3 לצורך תחזוקה) ושלפוחית ​​השתן שלה נחשף על ידי ביצוע חתך בבטן קו האמצע עם מספריים. אם השלפוחית ​​מלאה, היא decompressed חלקית על ידי סחיטה עדינה בין שתי אצבעות. ההשעיה התא עניין מוזרק intramurally בקיר הכיפה שלפוחית ​​השתן באמצעות מחט 29 או 30 מד 1 סמ&quot;ק או מזרק קטן. הפצע סגור ולאחר מכן באמצעות קליפים הפצע העכבר מותר להתאושש על כרית חימום. קיר הזרקת שלפוחית ​​השתן היא טכניקה microsurgical עדין שניתן לשליטה באמצעות תרגול.

Watch this Scientific Journal Video about Mouse Bladder Wall Injection at JoVE.com

Mouse Bladder Wall Injection

שלפוחית ​​השתן עכבר הזרקת הקיר היא גישה יעילה orthotopically מחקר גזע שלפוחית ​​השתן התא וביולוגיה סרטן. שיטה זו microsurgical עדין ניתן לשלוט בטכניקה תרגול זהיר.

שלפוחית ​​השתן עכבר וול Injection

Mouse bladder wall injection is a useful technique to orthotopically study bladder phenomena, including stem cell, smooth muscle, and cancer biology. ...

Research

JoVE Journal

Medicine

23.8K Views.  Stanford University School of Medicine. שלפוחית ​​השתן עכבר הזרקת הקיר היא גישה יעילה orthotopically מחקר גזע שלפוחית ​​השתן התא וביולוגיה סרטן. שיטה זו microsurgical עדין ניתן לשלוט בטכניקה תרגול זהיר.

Video: Mouse Bladder Wall Injection

An Orthotopic Model of Murine Bladder Cancer

In this straightforward procedure, bladder tumors are established in female C57 mice through the use of catheterization, local cauterization, and subsequent cell adhesion. After their bladders are transurethrally catheterized and drained, animals are again catheterized to permit insertion of a platinum wire into bladders without damaging the urethra or bladder. The catheters are made of Teflon to serve as an insulator for the wire, which will conduct electrical current into the bladder to create a burn injury. An electrocautery unit is used to deliver 2.5W to the exposed end of the wire, burning away extracellular layers and providing attachment sites for carcinoma cells that are delivered in suspension to the bladder through a subsequent catheterization. Cells remain in the bladder for 90 minutes, after which the catheters are removed and the bladders allowed to drain naturally. The development of tumor is monitored via ultrasound. Specific attention is paid to the catheterization technique in the accompanying video.

Bladder tumors are established in female mice in a minimally invasive fashion through catheterization, local cauterization, and subsequent adhesion of carcinoma cells to the burn sites.

דגם orthotopic של סרטן שלפוחית ​​השתן Murine

In this straightforward procedure, bladder tumors are established in female C57 mice through the use of catheterization, local cauterization, and ...

The Use of Cystometry in Small Rodents: A Study of Bladder Chemosensation

The lower urinary tract (LUT) functions as a dynamic reservoir that is able to store urine and to efficiently expel it at a convenient time. While storing urine, however, the bladder is exposed for prolonged periods to waste products. By acting as a tight barrier, the epithelial lining of the LUT, the urothelium, avoids re-absorption of harmful substances. Moreover, noxious chemicals stimulate the bladder's nociceptive innervation and initiate voiding contractions that expel the bladder's contents. Interestingly, the bladder's sensitivity to noxious chemicals has been used successfully in clinical practice, by intravesically infusing the TRPV1 agonist capsaicin to treat neurogenic bladder overactivity1. This underscores the advantage of viewing the bladder as a chemosensory organ and prompts for further clinical research. However, ethical issues severely limit the possibilities to perform, in human subjects, the invasive measurements that are necessary to unravel the molecular bases of LUT clinical pharmacology. A way to overcome this limitation is the use of several animal models2. Here we describe the implementation of cystometry in mice and rats, a technique that allows measuring the intravesical pressure in conditions of controlled bladder perfusion.
	After laparotomy, a catheter is implanted in the bladder dome and tunneled subcutaneously to the interscapular region. Then the bladder can be filled at a controlled rate, while the urethra is left free for micturition. During the repetitive cycles of filling and voiding, intravesical pressure can be measured via the implanted catheter. As such, the pressure changes can be quantified and analyzed. Moreover, simultaneous measurement of the voided volume allows distinguishing voiding contractions from non-voiding contractions3.
	Importantly, due to the differences in micturition control between rodents and humans, cystometric measurements in these animals have only limited translational value4. Nevertheless, they are quite instrumental in the study of bladder pathophysiology and pharmacology in experimental pre-clinical settings. Recent research using this technique has revealed the key role of novel molecular players in the mechano- and chemo-sensory properties of the bladder.

Cystometry is an efficient technique to measure bladder function of small animals in vivo. The bladder is continuously infused at rates controlled through an intravesical catheter, whereas the urethra is left free for micturition. This allows for repetitive filling and emptying of the bladder, while intravesical pressure and voided volume are recorded.

השימוש בCystometry במכרסמים קטנים: חקר Chemosensation שלפוחית ​​השתן

	The lower urinary tract (LUT) functions as a  dynamic reservoir that is able to store urine and to efficiently expel it at a  convenient time. While ...

Intraductal Injection of LPS as a Mouse Model of Mastitis: Signaling Visualized via an NF-&kappa;B Reporter Transgenic

Animal models of human disease are necessary in order to rigorously study stages of disease progression and associated mechanisms, and ultimately, as pre-clinical models to test interventions. In these methods, we describe a technique in which lipopolysaccharide (LPS) is injected into the lactating mouse mammary gland via the nipple, effectively modeling mastitis, or inflammation, of the gland. This simulated infection results in increased nuclear factor kappa B (NF-&kappa;B) signaling, as visualized through bioluminescent imaging of an NF-&kappa;B luciferase reporter mouse1.
Our ultimate goal in developing these methods was to study the inflammation associated with mastitis in the lactating gland, which often includes redness, swelling, and immune cell infiltration2,3. Therefore, we were keenly aware that incision or any type of wounding of the skin, the nipple, or the gland in order to introduce the LPS could not be utilized in our methods since the approach would likely confound the read-out of inflammation. We also desired a straight-forward method that did not require specially made hand-drawn pipettes or the use of micromanipulators to hold these specialized tools in place. Thus, we determined to use a commercially available insulin syringe and to inject the agent into the mammary duct of an intact nipple. This method was successful and allowed us to study the inflammation associated with LPS injection without any additional effects overlaid by the process of injection. In addition, this method also utilized an NF-&kappa;B luciferase reporter transgenic mouse and bioluminescent imaging technology to visually and quantitatively show increased NF-&kappa;B signaling within the LPS-injected gland4.
These methods are of interest to researchers of many disciplines who wish to model disease within the lactating mammary gland, as ultimately, the technique described here could be utilized for injection of a number of substances, and is not limited to only LPS.

Intraductal Injection of LPS as a Mouse Model of Mastitis: Signaling Visualized via an NF-&amp;kappa;B Reporter Transgenic

Described here is a technique in which lipopolysaccharide is injected into the lactating mouse mammary gland via the nipple to simulate mastitis, a condition commonly caused by bacterial infection. Lipopolysaccharide injection results in increased nuclear factor kappa B (NF-&kappa;B) signaling, visualized through bioluminescent imaging of an NF-&kappa;B luciferase reporter mouse.

הזרקת Intraductal של LPS כמודל עכבר של דלקת בשד: איתות מדמיינת דרך NF-κB כתב מהונדס

Animal models of human disease are necessary in order to rigorously study stages of disease progression and associated mechanisms, and ultimately, as ...

An Orthotopic Bladder Tumor Model and the Evaluation of Intravesical saRNA Treatment

We present a novel method for treating bladder cancer with intravesically delivered small activating RNA (saRNA) in an orthotopic xenograft mouse bladder tumor model. The mouse model is established by urethral catheterization under inhaled general anesthetic. Chemical burn is then introduced to the bladder mucosa using intravesical silver nitrate solution to disrupt the bladder glycosaminoglycan layer and allows cells to attach. Following several washes with sterile water, human bladder cancer KU-7-luc2-GFP cells are instilled through the catheter into the bladder to dwell for 2 hours. Subsequent growth of bladder tumors is confirmed and monitored by in vivo bladder ultrasound and bioluminescent imaging. The tumors are then treated intravesically with saRNA formulated in lipid nanoparticles (LNPs). Tumor growth is monitored with ultrasound and bioluminescence. All steps of this procedure are demonstrated in the accompanying video.

Establishing an orthotopic bladder tumor model to evaluate antitumor effects of intravesically delivered saRNA and monitoring tumor growth by ultrasound and bioluminescent imaging.

שלפוחית ​​השתן Orthotopic גידול דגם ואת הערכת טיפול סרנה השלפוחית

We present a novel method for treating bladder cancer with intravesically delivered small activating RNA (saRNA) in an orthotopic xenograft mouse bladder ...

Subretinal Injection of Gene Therapy Vectors and Stem Cells in the Perinatal Mouse Eye

The loss of sight affects approximately 3.4 million people in the United States and is expected to increase in the upcoming years.1 Recently, gene therapy and stem cell transplantations have become key therapeutic tools for treating blindness resulting from retinal degenerative diseases. Several forms of autologous transplantation for age-related macular degeneration (AMD), such as iris pigment epithelial cell transplantation, have generated encouraging results, and human clinical trials have begun for other forms of gene and stem cell therapies.2 These include RPE65 gene replacement therapy in patients with Leber's congenital amaurosis and an RPE cell transplantation using human embryonic stem (ES) cells in Stargardt's disease.3-4 Now that there are gene therapy vectors and stem cells available for treating patients with retinal diseases, it is important to verify these potential therapies in animal models before applying them in human studies. The mouse has become an important scientific model for testing the therapeutic efficacy of gene therapy vectors and stem cell transplantation in the eye.5-8 In this video article, we present a technique to inject gene therapy vectors or stem cells into the subretinal space of the mouse eye while minimizing damage to the surrounding tissue.

This surgical technique illustrates the injection of gene therapy vectors and stem cells into the subretinal space of the mouse eye.

הזרקת subretinal של וקטורי ריפוי גנטי ותאי גזע לעיניים המאוסות

The loss of sight affects approximately 3.4 million people in the United States and is expected to increase in the upcoming years.1 Recently, gene therapy ...

Reduction in Left Ventricular Wall Stress and Improvement in Function in Failing Hearts using Algisyl-LVR

Injection of Algisyl-LVR, a treatment under clinical development, is intended to treat patients with dilated cardiomyopathy. This treatment was recently used for the first time in patients who had symptomatic heart failure. In all patients, cardiac function of the left ventricle (LV) improved significantly, as manifested by consistent reduction of the LV volume and wall stress. Here we describe this novel treatment procedure and the methods used to quantify its effects on LV wall stress and function.
Algisyl-LVR is a biopolymer gel consisting of Na+-Alginate and Ca2+-Alginate. The treatment procedure was carried out by mixing these two components and then combining them into one syringe for intramyocardial injections. This mixture was injected at 10 to 19 locations mid-way between the base and apex of the LV free wall in patients.
Magnetic resonance imaging (MRI), together with mathematical modeling, was used to quantify the effects of this treatment in patients before treatment and at various time points during recovery. The epicardial and endocardial surfaces were first digitized from the MR images to reconstruct the LV geometry at end-systole and at end-diastole. Left ventricular cavity volumes were then measured from these reconstructed surfaces.
Mathematical models of the LV were created from these MRI-reconstructed surfaces to calculate regional myofiber stress. Each LV model was constructed so that 1) it deforms according to a previously validated stress-strain relationship of the myocardium, and 2) the predicted LV cavity volume from these models matches the corresponding MRI-measured volume at end-diastole and end-systole. Diastolic filling was simulated by loading the LV endocardial surface with a prescribed end-diastolic pressure. Systolic contraction was simulated by concurrently loading the endocardial surface with a prescribed end-systolic pressure and adding active contraction in the myofiber direction. Regional myofiber stress at end-diastole and end-systole was computed from the deformed LV based on the stress-strain relationship.

This article describes procedures for implanting a novel hydrogel in failing hearts and quantifying its effect on left ventricular wall stress and function. These procedures have been successfully applied in dogs and humans.

ירידה במתח וול חדר שמאלי ושיפור בתפקוד בכישלון לבבות באמצעות Algisyl-LVR

Injection of  Algisyl-LVR, a treatment under clinical development, is intended to treat  patients with dilated cardiomyopathy. This treatment was recently ...

An Orthotopic Bladder Cancer Model for Gene Delivery Studies

Bladder cancer is the second most common cancer of the urogenital tract and novel therapeutic approaches that can reduce recurrence and progression are needed. The tumor microenvironment can significantly influence tumor development and therapy response. It is therefore often desirable to grow tumor cells in the organ from which they originated. This protocol describes an orthotopic model of bladder cancer, in which MB49 murine bladder carcinoma cells are instilled into the bladder via catheterization. Successful tumor cell implantation in this model requires disruption of the protective glycosaminoglycan layer, which can be accomplished by physical or chemical means. In our protocol the bladder is treated with trypsin prior to cell instillation. Catheterization of the bladder can also be used to deliver therapeutics once the tumors are established. This protocol describes the delivery of an adenoviral construct that expresses a luciferase reporter gene. While our protocol has been optimized for short-term studies and focuses on gene delivery, the methodology of mouse bladder catheterization has broad applications.

Implantation of cancer cells into the organ of origin can serve as a useful preclinical model to evaluate novel therapies. MB49 bladder carcinoma cells can be grown within the bladder following intravesical instillation. This protocol demonstrates catheterization of the mouse bladder for the purpose of tumor implantation and adenoviral delivery.

סרטן שלפוחית ​​השתן לדגם orthotopic ג&#39;ין משלוח לימודים

Bladder cancer is the second most common cancer of the urogenital tract and novel therapeutic approaches that can reduce recurrence and progression are ...

Minimally Invasive Establishment of Murine Orthotopic Bladder Xenografts

Orthotopic bladder cancer xenografts are the gold standard to study molecular cellular manipulations and new therapeutic agents&#160;in vivo. Suitable cell lines are inoculated either by intravesical instillation (model of nonmuscle invasive growth) or intramural injection into the bladder wall (model of invasive growth). Both procedures are complex and highly time-consuming. Additionally, the superficial model has its shortcomings due to the lack of cell lines that are tumorigenic following instillation. Intramural injection, on the other hand, is marred by the invasiveness of the procedure and the associated morbidity for the host mouse.
With these shortcomings in mind, we modified previous methods to develop a minimally invasive approach for creating orthotopic bladder cancer xenografts. Using ultrasound guidance we have successfully performed percutaneous inoculation of the bladder cancer cell lines UM-UC1, UM-UC3 and UM-UC13 into 50 athymic nude. We have been able to demonstrate that this approach is time efficient, precise and safe. With this technique, initially a space is created under the bladder mucosa with PBS, and tumor cells are then injected into this space in a second step. Tumor growth is monitored at regular intervals with bioluminescence imaging and ultrasound. The average tumor volumes increased steadily in in all but one of our 50 mice over the study period.
In our institution, this novel approach, which allows bladder cancer xenograft inoculation in a minimally-invasive, rapid and highly precise way, has replaced the traditional model.

The established technique to inoculate primary invasive orthotopic bladder cancer xenografts requires laparotomy and mobilization of the bladder. This procedure inflicts significant morbidity on the mice, is technically challenging and time-consuming. We therefore developed a high-precision, percutaneous approach utilizing ultrasound guidance.

פולשנית הקמת Murine Orthotopic שלפוחית ​​השתן xenografts

Orthotopic bladder cancer xenografts are the gold standard to study molecular cellular manipulations and new therapeutic agents&#160;in vivo. Suitable ...

Urinary Bladder Distention Evoked Visceromotor Responses as a Model for Bladder Pain in Mice

Approximately 3-8 million people in the United States suffer from interstitial cystitis/bladder pain syndrome (IC/BPS), a debilitating condition characterized by increased urgency and frequency of urination, as well as nocturia and general pelvic pain, especially upon bladder filling or voiding. Despite years of research, the cause of IC/BPS remains elusive and treatment strategies are unable to provide complete relief to patients. In order to study nervous system contributions to the condition, many animal models have been developed to mimic the pain and symptoms associated with IC/BPS. One such murine model is urinary bladder distension (UBD). In this model, compressed air of a specific pressure is delivered to the bladder of a lightly anesthetized animal over a set period of time. Throughout the procedure, wires in the superior oblique abdominal muscles record electrical activity from the muscle. This activity is known as the visceromotor response (VMR) and is a reliable and reproducible measure of nociception. Here, we describe the steps necessary to perform this technique in mice including surgical manipulations, physiological recording, and data analysis. With the use of this model, the coordination between primary sensory neurons, spinal cord secondary afferents, and higher central nervous system areas involved in bladder pain can be unraveled. This basic science knowledge can then be clinically translated to treat patients suffering from IC/BPS.

Approximately 3-8 million people in the United States suffer from interstitial cystitis/bladder pain syndrome (IC/BPS), a debilitating condition characterized in part by pelvic pain. In order to study nervous system contributions to the condition, a physiological model of urinary bladder pain is used in mice and rats.

תגובות שתן בשלפוחית ​​השתן ההתנפחות העוררת Visceromotor כמודל לשלפוחית ​​שתן כאב בעכברים

Approximately 3-8 million people in the United States suffer from interstitial cystitis/bladder pain syndrome (IC/BPS), a debilitating condition ...

Ultrahigh Resolution Mouse Optical Coherence Tomography to Aid Intraocular Injection in Retinal Gene Therapy Research

HR-SD-OCT is utilized to monitor the progression of photoreceptor degeneration in live mouse models, assess the delivery of therapeutic agents into the subretinal space, and to evaluate toxicity and efficacy in vivo. HR-SD-OCT uses near infrared light (800-880 nm) and has optics specifically designed for the unique optics of the mouse eye with sub-2-micron axial resolution. Transgenic mouse models of outer retinal (photoreceptor) degeneration and controls were imaged to assess the disease progression. Pulled glass microneedles were used to deliver sub retinal injections of adeno-associated virus (AAV) or nanoparticles (NP) via a trans-scleral and trans-choroidal approach. Careful positioning of the needle into the subretinal space was required prior to a calibrated pressure injection, which delivers fluid into the sub retinal space. Real time subretinal surgery was conducted on our retinal imaging system (RIS). HR-SD-OCT demonstrated progressive uniform retinal degeneration due to expression of a toxic mutant human mutant rhodopsin (P347S) (RHOP347S) transgene in mice. HR-SD-OCT allows rigorous quantification of all the retinal layers. Outer nuclear layer (ONL) thickness and photoreceptor outer segment length (OSL) measurements correlate with photoreceptor vitality, degeneration, or rescue. The RIS delivery system allows real-time visualization of subretinal injections in neonatal (~P10-14) or adult mice, and HR-SD-OCT immediately determines success of delivery and maps areal extent. HR-SD-OCT is a powerful tool that can evaluate the success of subretinal surgery in mice, in addition to measuring vitality of photoreceptors in vivo. HR-SD-OCT can also be used to identify uniform animal cohorts to evaluate the extent of retinal degeneration, toxicity, and therapeutic rescue in preclinical gene therapy research studies.

Here we demonstrate a novel approach to using high resolution spectral-domain optical coherence tomography (HR-SD-OCT) to assist delivery of gene therapy agents into the subretinal space, assess its areal coverage, and characterize photoreceptor vitality.

טומוגרפיה אופטית קוהרנטית העכבר הרזולוציה על קוליים כדי לסייע הזרקה תוך-עיני במחקר ריפוי גנטי ברשתית

HR-SD-OCT is utilized to monitor the progression of photoreceptor degeneration in live mouse models, assess the delivery of therapeutic agents into the ...

שלפוחית ​​השתן עכבר וול Injection

שלפוחית השתן עכבר וול Injection