Summary

قياس صلابة من<em> فيفو السابقين</em> ماوس Aortas باستخدام مجهر القوة الذرية

Published: October 19, 2016
doi:

Summary

We present detailed protocols for isolation of aortas from mouse and measurement of their elastic modulus using atomic force microscopy.

Abstract

تشنج الشرايين هو عامل خطر كبير والعلامات البيولوجية لمرض القلب والأوعية الدموية والسمة المميزة للشيخوخة. مجهر القوة الذرية (AFM) هو أداة تحليلية متعددة لوصف الخواص الميكانيكية اللزجة لمجموعة متنوعة من المواد تتراوح ما بين الصلب (البلاستيك والزجاج والمعادن، الخ) السطوح إلى خلايا في أي الركيزة. وقد استخدم على نطاق واسع لقياس صلابة من الخلايا، ولكنها أقل استخداما لقياس صلابة من aortas. في هذه الورقة، فإننا سوف تصف إجراءات استخدام AFM في وضع الاتصال لقياس خارج الجسم الحي معامل مرونة الشرايين الماوس المفرغة. وصفنا إجراءاتنا لعزل aortas الماوس، ثم تقديم معلومات مفصلة لتحليل فؤاد. وهذا يشمل إرشادات خطوة بخطوة لمحاذاة شعاع الليزر، معايرة ثابت الربيع وحساسية انحراف لجنة التحقيق AFM، والحصول على منحنيات القوة. ونحن نقدم أيضا بروتوكول مفصلة لanaly البياناتجهاز الأمن والمخابرات من منحنيات القوة.

Introduction

The biomechanical properties of arteries are a critical determinant in cardiovascular disease (CVD) and aging. Arterial stiffness, a major cholesterol independent risk factor and an indicator for the progression of CVD, increases with vascular injury, atherosclerosis, age, and diabetes1-8. Arterial wall stiffening is associated with increased dedifferentiation, migration, and proliferation of vascular smooth muscle cells9-12. In addition, increased arterial stiffness has been linked to enhanced macrophage adhesion1, endothelial permeability and leukocyte transmigration13, and vessel wall remodeling14,15. Thus, therapies that could prevent arterial stiffening in CVD or aging might complement currently available pharmacological interventions that treat CVD by reducing high blood cholesterol.

AFM is a powerful analytical tool used for various physical and biological applications. AFM is increasingly used to obtain the high-resolution images and characterize the biomechanical properties of soft biological samples such as tissues and cells1,2,10,16,17 with a great degree of accuracy at nanoscale levels. A major advantage of AFM is the fact that it can be used with living cells.

This paper describes our method for measuring the elastic modulus of mouse arteries ex vivo using AFM. The described method shows how we 1) properly isolate mouse arteries (descending aorta and aortic arch) and 2) measure the elastic modulus of these tissues by AFM. Measurements of unloaded elastic moduli in arteries can help to elucidate changes in the extracellular matrix (ECM) that occur in response to vascular injury, CVD, and aging.

Protocol

وقد وافق العمل حيوان في هذه الدراسة من قبل لجان رعاية واستخدام الحيوان المؤسسي من جامعة ولاية بنسلفانيا. نفذت الطرق وفقا للمبادئ التوجيهية المعتمدة. 1. إعداد الماوس وعزل الشريان الأورطي <li style=";text-align:right;dir…

Representative Results

ويبين الشكل 5A صورة النقيض مرحلة من الشريان الأورطي النازل (الصدر) من العمر 6 أشهر، الذكور C57BL / 6 الماوس. ناتئ فؤاد في مكان مباشرة فوق الأنسجة وجاهزة للتسنن. الأرقام 5B و5C تظهر منحنيات القوة التمثيلية التي حصلت عليها AFM المسافة البادئة في وض…

Discussion

فؤاد المسافة البادئة يمكن استخدامها لتوصيف صلابة (معامل المرونة) من الخلايا والأنسجة. في هذه الورقة، ونحن نقدم تفصيلا بروتوكولات خطوة بخطوة لعزل الشريان الأورطي النازل وقوس الأبهر في الماوس وتحديد الرجوعية المرنة من هذه المناطق الشرايين خارج الحي. نحن الآن تلخ…

Disclosures

The authors have nothing to disclose.

Acknowledgements

AFM analysis was performed on instrumentation supported by the Pennsylvania Muscle Institute and the Institute for Translational Medicine and Therapeutics, Perelman School of Medicine, the University of Pennsylvania. This work was supported by NIH grants HL62250 and AG047373. YHB was supported by post-doctoral fellowship from the American Heart Association.

Materials

BioScope Catalyst AFM system Bruker
Nikon Eclipse TE 200 inverted microscope Nikon Instruments
Silicon nitride AFM probe Novascan Technologies PT.SI02.SN.1 0.06 N/m cantilever; 1 µm SiO2 particle
Dumont #5 forceps Fine Science Tools 11251-10 See section 1.4
Dumont #5SF forceps Fine Science Tools 11252-00 See section 1.8
Fine Scissors-ToughCut Fine Science Tools 14058-11 See section 1.4 (medium sized)
Vannas-Tübingen spring scissors Fine Science Tools 15008-08 See section 1.6 (small sized)
60mmTC-treated cell culture dish Corning 353004
Dulbecco's Phosphate-Buffered Saline, 1X Corning 21-031-CM Without calcium and magnesium
Krazy Glue instant all purpose liquid Krazy Glue KG58548R See section 2.2
Gel-loading tips, 1-200 µL Fisher 02-707-139 See section 2.2
Tip Tweezers Electron Microscopy Sciences 78092-CP See section 3.2
50-mm, clear wall glass bottom dishes TED PELLA 14027-20 See section 4.4

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Cite This Article
Bae, Y. H., Liu, S., Byfield, F. J., Janmey, P. A., Assoian, R. K. Measuring the Stiffness of Ex Vivo Mouse Aortas Using Atomic Force Microscopy. J. Vis. Exp. (116), e54630, doi:10.3791/54630 (2016).

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