Production year
2017
© Hugues LELOUARD / CIML / INSERM / CNRS Images
20170103_0001
Small intestine of a mouse, observed using multicolour confocal microscopy. Immunofluorescent marking reveals epithelial cells in cyan, blood vessels in magenta, lymph vessels in orange, phagocytic cells in red, monocytes in green, paneth cells and mucus in grey, collagen fibres in yellow, and lastly, actin filaments in purple. The image was obtained by combining several lasers and a spectral detector able to distinguish a wide range of fluorochromes, i.e. colours. A high-power (40X) oil-immersion objective lens was used. With confocal microscopy, laser beams scan the specimen at high speed, point by point. This technique can be used to produce thin optical cross-sections (at various specimen thicknesses) that reveal the locations of numerous entities and cell types (T and B lymphocytes, dendrites, macrophages, actins, nuclei, etc.) in a tissue slice. These optical cross-sections are then stacked to generate 3D images of the specimens. This enables scientists to compare the locations and numbers of entities in various circumstances, such as in patients suffering from diseases, for example, in order to shed light on the workings of the immune system. This technique is constantly being improved in terms of its resolution and sensitivity, as well as the possible colours and contrasts.
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2017
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