TY - JOUR
T1 - Ultrasonic intensity microscopy for imaging of living cells
AU - Hagiwara, Yoshihiro
AU - Saijo, Yoshifumi
AU - Ando, Akira
AU - Chimoto, Eiichi
AU - Suda, Hideaki
AU - Onoda, Yoshito
AU - Itoi, Eiji
PY - 2009/3
Y1 - 2009/3
N2 - Ultrasound intensity microscopy was developed for in vivo imaging. This paper describes the preliminary results obtained using 300 MHz ultrasound intensity microscopy for in vitro characterization of cell cultures. The novelty of the approach lies in the fact that it allows remote, non-contact and disturbance-free imaging of cultured synovial cells and the changes in the cells' properties due to external stimulants such as transforming growth factor beta-1 (TGF-β1). The intensity imaging method has potential for extracting mechanical cell properties and monitoring the effects of drugs. Ultrasound propagates through a thin specimen such as cultured cells and is reflected at the interface between the specimen and substrate. A two-dimensional distribution of the ultrasonic intensity, which is closely related to the mechanical properties, is visualized to analyze cell organs, such as the nucleus at the central part and the cytoskeleton at the peripheral zone. After stimulation with TGF-β1, the ultrasonic intensity at the actin zone was significantly increased compared with the control.
AB - Ultrasound intensity microscopy was developed for in vivo imaging. This paper describes the preliminary results obtained using 300 MHz ultrasound intensity microscopy for in vitro characterization of cell cultures. The novelty of the approach lies in the fact that it allows remote, non-contact and disturbance-free imaging of cultured synovial cells and the changes in the cells' properties due to external stimulants such as transforming growth factor beta-1 (TGF-β1). The intensity imaging method has potential for extracting mechanical cell properties and monitoring the effects of drugs. Ultrasound propagates through a thin specimen such as cultured cells and is reflected at the interface between the specimen and substrate. A two-dimensional distribution of the ultrasonic intensity, which is closely related to the mechanical properties, is visualized to analyze cell organs, such as the nucleus at the central part and the cytoskeleton at the peripheral zone. After stimulation with TGF-β1, the ultrasonic intensity at the actin zone was significantly increased compared with the control.
KW - Cell
KW - Imaging
KW - Mechanical property
KW - Synovial tissue
KW - TGF-β1
KW - Ultrasound intensity microscopy
UR - http://www.scopus.com/inward/record.url?scp=60549117678&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=60549117678&partnerID=8YFLogxK
U2 - 10.1016/j.ultras.2008.10.013
DO - 10.1016/j.ultras.2008.10.013
M3 - Article
C2 - 19062059
AN - SCOPUS:60549117678
SN - 0041-624X
VL - 49
SP - 386
EP - 388
JO - Ultrasonics
JF - Ultrasonics
IS - 3
ER -