Background: Natural killer (NK) cells produce multiple cytokines with potential immune regulatory roles. We standardised a whole-blood flow cytometry method to visualise intracellular cytokine production by NK cells for the study of NK cell biology and for clinical monitoring. Methods: With a three-
Flow cytometric differentiation of erythrocytes and leukocytes in dilute whole blood by light scattering
โ Scribed by V. Ost; J. Neukammer; H. Rinneberg
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 132 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0196-4763
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โฆ Synopsis
We have determined differential scattering cross sections of sphered erythrocytes integrated over the solid angle accepted by our detectors at wavelengths varying between 379.5-632.8 nm, employing Ar+-, Kr+-, and HeNe-laser radiation. Integrated differential cross sections for forward and orthogonal light scatter exhibit a pronounced minimum at about lambda = 413 nm, caused by the strong absorption of light by oxyhemoglobin. Experimental data are in good agreement with values calculated by the Mie theory. Simultaneous measurements of forward and orthogonal light scatter using Kr+-laser radiation (lambda = 413.1 nm) allow flow cytometric differentiation of (native) erythrocytes, thrombocytes, and leukocytes as well as subpopulations of leukocytes, i.e., granulocytes, lymphocytes, and monocytes in dilute whole-blood samples. Lysis of red blood cells or staining of white blood cells is not required to obtain absolute leukocyte counts or differential white blood cell counts.
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