TY - JOUR
T1 - Multiphoton microscopy in defining liver function
AU - Thorling, Camilla A.
AU - Crawford, Darrell
AU - Burczynski, Frank J.
AU - Liu, Xin
AU - Liau, Ian
AU - Roberts, Michael S.
PY - 2014/9/1
Y1 - 2014/9/1
N2 - Multiphoton microscopy is the preferred method when in vivo deep-tissue imaging is required. This review presents the application of multiphoton microscopy in defining liver function. In particular, multiphoton microscopy is useful in imaging intracellular events, such as mitochondrial depolarization and cellular metabolism in terms of NAD(P)H changes with fluorescence lifetime imaging microscopy. The morphology of hepatocytes can be visualized without exogenously administered fluorescent dyes by utilizing their autofluorescence and second harmonic generation signal of collagen, which is useful in diagnosing liver disease. More specific imaging, such as studying drug transport in normal and diseased livers are achievable, but require exogenously administered fluorescent dyes. If these techniques can be translated into clinical use to assess liver function, it would greatly improve early diagnosis of organ viability, fibrosis, and cancer.
AB - Multiphoton microscopy is the preferred method when in vivo deep-tissue imaging is required. This review presents the application of multiphoton microscopy in defining liver function. In particular, multiphoton microscopy is useful in imaging intracellular events, such as mitochondrial depolarization and cellular metabolism in terms of NAD(P)H changes with fluorescence lifetime imaging microscopy. The morphology of hepatocytes can be visualized without exogenously administered fluorescent dyes by utilizing their autofluorescence and second harmonic generation signal of collagen, which is useful in diagnosing liver disease. More specific imaging, such as studying drug transport in normal and diseased livers are achievable, but require exogenously administered fluorescent dyes. If these techniques can be translated into clinical use to assess liver function, it would greatly improve early diagnosis of organ viability, fibrosis, and cancer.
KW - drug transport
KW - fibrosis
KW - fluorescence lifetime imaging microscopy
KW - hepatocellular carcinoma
KW - mitochondria
KW - multiphoton microscopy
KW - nanoparticles
KW - second harmonic generation
UR - http://www.scopus.com/inward/record.url?scp=84911465916&partnerID=8YFLogxK
U2 - 10.1117/1.JBO.19.9.090901
DO - 10.1117/1.JBO.19.9.090901
M3 - Review article
C2 - 25200392
AN - SCOPUS:84911465916
SN - 1083-3668
VL - 19
JO - Journal of Biomedical Optics
JF - Journal of Biomedical Optics
IS - 9
M1 - 090901
ER -