4.6 Article

Imaging erythrocyte sedimentation in whole blood

期刊

FRONTIERS IN PHYSIOLOGY
卷 13, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.1101/2021.08.31.458375

关键词

red cells; erythrocyte sedimentation rate (ESR); mesoscopic microscopy; 2-photon microscopy; light-sheet microscopy; colloidal gel

资金

  1. Deutsche Forschungsgemeinschaft (DFG)
  2. European Union [860436 -EVIDENCE]
  3. French German University (DFH/UFA)
  4. Deutsche Forschungsgemeinschaft (DFG, German Research Foundation)
  5. Saarland University
  6. DFG [INST 256/423-1 FUGG]

向作者/读者索取更多资源

This study uses three different optical imaging techniques to observe the structures formed by erythrocytes in static blood. The results reveal a dynamic structure of a channeling gel, but with differences in the resolved details among the techniques. Further refinement of the experimental set-ups is required for a quantitative analysis of erythrocyte-related processes and interactions during sedimentation.
The erythrocyte sedimentation rate (ESR) is one of the oldest medical diagnostic tools. However, currently there is some debate on the structure formed by the cells during the sedimentation process. While the conventional view is that erythrocytes sediment as separate aggregates, others have suggested that they form a percolating gel, similar to other colloidal suspensions. A direct probing of the structures formed by erythrocytes in blood at stasis is then required to settle these discrepancies. Here, we report observations performed with three different optical imaging techniques: direct light transmission through thin samples, two-photon microscopy and light-sheet microscopy. All techniques revealed a dynamic structure of a channeling gel but with differences in the resolved details. A quantitative analysis of the erythrocyte related processes and interactions during the sedimentation need a further refinement of the experimental set-ups.

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