期刊文献+

Microscopic study of ultrasound-mediated microbubble destruction effects on vascular smooth muscle cells 被引量:2

Microscopic study of ultrasound-mediated microbubble destruction effects on vascular smooth muscle cells
下载PDF
导出
摘要 Objective:To observe vascular smooth muscle cell morphological changes induced by ultrasound combined with microbubbles by Atomic Force Acoustic Microscopy(AFAM).Methods:A7r5 rat aortic smooth muscle cells were divided into groups:control group(without ultrasonic irradiation,no micro bubbles)and US+MB group(45 kHz、0.4 W/cm^2 ultrasound irradiate for 20 seconds with a SonoVuc^(TM)concentration of[(56-140)×10~5/mL].Cell micromorphological changes(such as topographic and acoustic prognosis)were detected,before and after ultrasound destruction by AFAM.Results:In cell morphology,smooth muscle cells were spread o and connected to each another by fibers.At the center of the cell,the nuclear area had a rough surface and was significantly elevated from its surroundings.The cytoskeletal structure of the reticular nucleus and cytoplasm in the morphology of A7r5 cells(20μm×20μm)were clear before microbubble intervention.After acoustic exciting,the cell structure details of the acoustic image were improved with better resolution,showing the elasticity of different tissues.In the acoustic image,the nucleus was harder,more flexible and uneven compared with the cytoplasm.Many strong various-sized echo particles were stuck on the rough nuclear membrane's substrate surface.The nuclear membrane did not have a continuous smooth surface;there were many obstructions(pores).After ultrasound-intervention was combined with microbubbles,the dark areas of the A7r5 cell images was increased in various sizes and degrees.The dark areas showed the depth or low altitudes of the lower regions,suggesting regional depressions.However,the location and scope of the acoustic image dark areas were not similar to those found in the topographic images.Therefore,it was likely that the dark areas,both from the topographic and acoustic images,were sound-holes.In addition,some cell nuclei become round in different degrees after irradiation.Conclusions:Atomic force microscopy and acoustic excitation method can noninvasively and completely display a cell's structure,connections and elastic properties at a nano scale in just several minutes.The dark areas,both from the topographic and acoustic images,may be sound-holes;therefore,it would be helpful if these sound-holes were found.These findings provide a relationship between cell apoptosis after ultrasound and microbubble ultrasound irradiation,and the sound-hole effect. Objective:To observe vascular smooth muscle cell morphological changes induced by ultrasound combined with microbubbles by Atomic Force Acoustic Microscopy(AFAM).Methods:A7r5 rat aortic smooth muscle cells were divided into groups:control group(without ultrasonic irradiation,no micro bubbles)and US+MB group(45 kHz、0.4 W/cm2 ultrasound irradiate for 20 seconds with a SonoVucTMconcentration of[(56-140)×105/mL].Cell micromorphological changes(such as topographic and acoustic prognosis)were detected,before and after ultrasound destruction by AFAM.Results:In cell morphology,smooth muscle cells were spread o and connected to each another by fibers.At the center of the cell,the nuclear area had a rough surface and was significantly elevated from its surroundings.The cytoskeletal structure of the reticular nucleus and cytoplasm in the morphology of A7r5 cells(20μm×20μm)were clear before microbubble intervention.After acoustic exciting,the cell structure details of the acoustic image were improved with better resolution,showing the elasticity of different tissues.In the acoustic image,the nucleus was harder,more flexible and uneven compared with the cytoplasm.Many strong various-sized echo particles were stuck on the rough nuclear membrane’s substrate surface.The nuclear membrane did not have a continuous smooth surface;there were many obstructions(pores).After ultrasound-intervention was combined with microbubbles,the dark areas of the A7r5 cell images was increased in various sizes and degrees.The dark areas showed the depth or low altitudes of the lower regions,suggesting regional depressions.However,the location and scope of the acoustic image dark areas were not similar to those found in the topographic images.Therefore,it was likely that the dark areas,both from the topographic and acoustic images,were sound-holes.In addition,some cell nuclei become round in different degrees after irradiation.Conclusions:Atomic force microscopy and acoustic excitation method can noninvasively and completely display a cell’s structure,connections and elastic properties at a nano scale in just several minutes.The dark areas,both from the topographic and acoustic images,may be sound-holes;therefore,it would be helpful if these sound-holes were found.These findings provide a relationship between cell apoptosis after ultrasound and microbubble ultrasound irradiation,and the sound-hole effect.
出处 《Asian Pacific Journal of Tropical Medicine》 SCIE CAS 2015年第4期325-329,共5页 亚太热带医药杂志(英文版)
基金 supported by Shanghai Pudong New Area Health Plan Committee Of Academic Leaders Project(NO.PWRd2013-02) National Natural Fund(NO.81401428)
关键词 Atomic force acoustic microscopy VASCULAR SMOOTH muscle cell ULTRASOUND MICROBUBBLE Atomic force acoustic microscopy Vascular smooth muscle cell Ultrasound Microbubble
  • 相关文献

参考文献12

  • 1A. Ebert,B.R. Tittmann,J. Du,W. Scheuchenzuber.Technique for rapid in vitro single-cell elastography[J]. Ultrasound in Medicine & Biology . 2006 (11)
  • 2David O. Williams,Richard Holubkov,Wanlin Yeh,Martial G. Bourassa,Mahdi Al-Bassam,Peter C. Block,Paul Coady,Howard Cohen,Michael Cowley,Gerald Dorros,David Faxon,David R. Holmes,Alice Jacobs,Sheryl F. Kelsey,Spencer B. King,Richard Myler,James Slater,Vladimir Stanek,Helen A. Vlachos,Katherine M. Detre.Percutaneous Coronary Intervention in the Current Era Compared With 1985–1986: The National Heart, Lung, and Blood Institute Registries[J]. Circulation: Journal of the American Heart Association . 2000 (24)
  • 3Lopez AD.Assessing the burden of mortality from cardiovascular diseases. World Health Statistics Quarterly . 1993
  • 4D. A. Smith,I. Galin.Statin Therapy for Native and Peri-Interventional Coronary Heart Disease. Current Molecular Medicine . 2006
  • 5MU Hammer,A Brauser,C Olak,G Brezesinski,T Goldmann,T Gutsmann,J Andra?.Lipopolysaccharide interaction is decisive for the activity of the antimicrobial peptide NK-2 against Escherichia coli and Proteus mirabilis. The Biochemical Journal . 2010
  • 6Cretin, B.,Sthal, F.Scanning microdeformation microscopy. Applied Physics . 1993
  • 7Nowakowski, Robert,Luckham, Paul.Imaging the surface details of red blood cells with atomic force microscopy. Surface and Interface Analysis . 2002
  • 8Ashush H,Rozenszajn L A,Blass M,et al.Apoptosis induction of human myeloid leukemic cells by ultrasound exposure. Cancer Research . 2000
  • 9Paul P,Alfred C,Kishand D,et al.Membrane disruption by optically controlled microbubble cavitation. Nature Physics . 2005
  • 10Ebert AM,Du JK,Wang XW,et al.The elastic properties of hamster kidney cells evaluated by ultrasonic atomic force microscopy. IEEE Ultrasonics Symposium Proceedings . 2004

共引文献2

同被引文献19

引证文献2

二级引证文献6

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部