Second harmonic generation microscopy differentiates collagen type I and type III in diseased lung tissues

Author(s):  
Masaru Suzuki ◽  
Damian Kayra ◽  
W. Mark Elliott ◽  
James C. Hogg ◽  
Thomas Abraham
Author(s):  
Nirmal Mazumder ◽  
Fu-Jen Kao

Abstract The complete polarization state of second harmonic (SH) light was measured and characterized by collagen type I and skeletal muscle fiber using a Stokes vector-based SHG microscope. The polarization states of the SH signal are analyzed in a pixel-by-pixel manner and displayed through two dimensional (2D) Stokes vector images. Various polarization parameters are reconstructed using Stokes values to quantify the polarization properties of SH light. Also, the measurements are extended for different input polarization states to investigate the molecular structure of second harmonic generation (SHG) active molecules such as collagen type I and myosin.


2006 ◽  
Vol 91 (12) ◽  
pp. 4665-4677 ◽  
Author(s):  
Theodossis A. Theodossiou ◽  
Christopher Thrasivoulou ◽  
Chidi Ekwobi ◽  
David L. Becker

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Shukei Sugita ◽  
Takuya Suzumura ◽  
Akinobu Nakamura ◽  
Shinya Tsukiji ◽  
Yoshihiro Ujihara ◽  
...  

AbstractThe ratio of type III to type I collagen is important for properly maintaining functions of organs and cells. We propose a method to quantify the ratio of type III to total (type I + III) collagen (λIII) in a given collagen fiber bundle using second harmonic generation (SHG) light. First, the relationship between SHG light intensity and the λIII of collagen gels was examined, and the slope (k1) and SHG light intensity at 0% type III collagen (k2) were determined. Second, the SHG light intensity of a 100% type I collagen fiber bundle and its diameter (D) were measured, and the slope (k3) of the relationship was determined. The λIII in a collagen fiber bundle was estimated from these constants (k1-3) and SHG light intensity. We applied this method to collagen fiber bundles isolated from the media and adventitia of porcine thoracic aortas, and obtained λIII = 84.7% ± 13.8% and λIII = 17.5% ± 15.2%, respectively. These values concurred with those obtained with a typical quantification method using sodium dodecyl sulfate–polyacrylamide gel electrophoresis. The findings demonstrated that the method proposed is useful to quantify the ratio of type III to total collagen in a collagen fiber bundle.


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