| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
(2)/
(3) Tensors in Submicron-Scaled Bio-Tissues by Polarization Harmonics Optical Microscopy


* Department of Electrical Engineering and Graduate Institute of Electro-Optical Engineering, National Taiwan University, Taipei, Taiwan, Republic of China; and
Molecular and Cell Biology Division, Development Center for Biotechnology, Taipei, Taiwan, Republic of China
Correspondence: Address reprint requests to Chi-Kuang Sun, Tel.: 886-2-3366-5085; Fax: 866-2-2367-7467; E-mail: sun{at}cc.ee.ntu.edu.tw.
Optical second- and third-harmonic generations have attracted a lot of attention in the biomedical imaging research field recently due to their intrinsic sectioning ability and noninvasiveness. Combined with near-infrared excitation sources, their deep-penetration ability makes these imaging modalities suitable for tissue characterization. In this article, we demonstrate a polarization harmonics optical microscopy, or P-HOM, to study the nonlinear optical anisotropy of the nanometer-scaled myosin and actin filaments inside myofibrils. By using tight focusing we can avoid the phase-matching condition due to micron-scaled, high-order structures in skeletal muscle fibers, and obtain the submicron-scaled polarization dependencies of second/third-harmonic generation intensities on the inclination angle between the long axes of the filaments and the polarization direction of the linear polarized fundamental excitation laser light. From these dependencies, detailed information on the tensor elements of the second/third-order nonlinear susceptibilities contributed from the myosin/actin filaments inside myofibrils can thus be analyzed and obtained, reflecting the detailed arrangements and structures of the constructing biomolecules. By acquiring a whole, nonlinearly sectioned image with a submicron spatial resolution, we can also compare the polarization dependency and calculate the nonlinear susceptibilities over a large area of the tissue at the same timewhich not only provides statistical information but will be especially useful with complex specimen geometry.
This article has been cited by other articles:
![]() |
R. LaComb, O. Nadiarnykh, and P. J. Campagnola Quantitative Second Harmonic Generation Imaging of the Diseased State Osteogenesis Imperfecta: Experiment and Simulation Biophys. J., June 1, 2008; 94(11): 4504 - 4514. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Legare, C. Pfeffer, and B. R. Olsen The Role of Backscattering in SHG Tissue Imaging Biophys. J., August 15, 2007; 93(4): 1312 - 1320. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Fu, H. Wang, R. Shi, and J.-X. Cheng Second Harmonic and Sum Frequency Generation Imaging of Fibrous Astroglial Filaments in Ex Vivo Spinal Tissues Biophys. J., May 1, 2007; 92(9): 3251 - 3259. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. V. Plotnikov, A. C. Millard, P. J. Campagnola, and W. A. Mohler Characterization of the Myosin-Based Source for Second-Harmonic Generation from Muscle Sarcomeres Biophys. J., January 15, 2006; 90(2): 693 - 703. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Plotnikov, V. Juneja, A. B. Isaacson, W. A. Mohler, and P. J. Campagnola Optical Clearing for Improved Contrast in Second Harmonic Generation Imaging of Skeletal Muscle Biophys. J., January 1, 2006; 90(1): 328 - 339. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |