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Real-time polarization microscopy of fibrillar collagen in histopathology.
Keikhosravi, Adib; Shribak, Michael; Conklin, Matthew W; Liu, Yuming; Li, Bin; Loeffler, Agnes; Levenson, Richard M; Eliceiri, Kevin W.
Afiliación
  • Keikhosravi A; Laboratory for Optical and Computational Instrumentation, Department of Biomedical Engineering, University of Wisconsin-Madison, Madison, WI, 53706, USA.
  • Shribak M; Marine Biological Laboratory, University of Chicago, Woods Hole, MA, 02543, USA. mshribak@mbl.edu.
  • Conklin MW; Deparment of Cell and Regenerative Biology, University of Wisconsin-Madison, Madison, WI, 53706, USA.
  • Liu Y; Laboratory for Optical and Computational Instrumentation, Department of Biomedical Engineering, University of Wisconsin-Madison, Madison, WI, 53706, USA.
  • Li B; Laboratory for Optical and Computational Instrumentation, Department of Biomedical Engineering, University of Wisconsin-Madison, Madison, WI, 53706, USA.
  • Loeffler A; Morgridge Institute for Research, Madison, WI, 53715, USA.
  • Levenson RM; Department of Pathology, MetroHealth Medical Center, Cleveland, OH, 44109, USA.
  • Eliceiri KW; Department of Pathology and Laboratory Medicine, UC Davis Health, Sacramento, CA, 95817, USA.
Sci Rep ; 11(1): 19063, 2021 09 24.
Article en En | MEDLINE | ID: mdl-34561546
Over the past two decades, fibrillar collagen reorganization parameters such as the amount of collagen deposition, fiber angle and alignment have been widely explored in numerous studies. These parameters are now widely accepted as stromal biomarkers and linked to disease progression and survival time in several cancer types. Despite all these advances, there has not been a significant effort to make it possible for clinicians to explore these biomarkers without adding steps to the clinical workflow or by requiring high-cost imaging systems. In this paper, we evaluate previously described polychromatic polarization microscope (PPM) to visualize collagen fibers with an optically generated color representation of fiber orientation and alignment when inspecting the sample by a regular microscope with minor modifications. This system does not require stained slides, but is compatible with histological stains such as H&E. Consequently, it can be easily accommodated as part of regular pathology review of tissue slides, while providing clinically useful insight into stromal composition.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Colágenos Fibrilares / Microscopía de Polarización Idioma: En Revista: Sci Rep Año: 2021 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Colágenos Fibrilares / Microscopía de Polarización Idioma: En Revista: Sci Rep Año: 2021 Tipo del documento: Article