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Morphology and expression status investigations of specific surface markers on B‐cell chronic lymphocytic leukemia cells
Author(s) -
Niu Suli,
Chan Ryan,
Berini Pierre,
Wang Chen,
Zou Shan
Publication year - 2013
Publication title -
microscopy research and technique
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.536
H-Index - 118
eISSN - 1097-0029
pISSN - 1059-910X
DOI - 10.1002/jemt.22278
Subject(s) - chronic lymphocytic leukemia , morphology (biology) , biology , leukemia , cell , microbiology and biotechnology , cancer research , chemistry , immunology , genetics
The morphology of cells and expression status of specific surface markers [cluster of differentiation (CD)], such as CD5, CD19, CD20, CD38, and CD45, have long been considered as the essential indicators for the diagnosis and prognosis of B‐cell chronic lymphocytic leukemia (B‐CLL). Clinically, it is difficult to simultaneously obtain cell morphology and distribution of surface markers with flow cytometry, especially for some surrogate markers such as CD38. Here, as an alternative and complementary prognostic method, fluorescence microscopy and image processing method are introduced to directly visualize the cells from patients and to quantitatively determine the expression status of surface markers. In this study, the morphological parameters of B‐CLL cells were measured to establish the correlation between the cellular morphology and the surface marker expression. It was clear that the CD38+ and CD38− B‐CLL cells from the same CD38+ patients had hardly any size differences; however, an increase in perimeter was observed for CD38− patients. Moreover, the expression level of the receptors on the cell was independent of the cell size. There was no evidence showing that the expression intensities of CD19 and CD38 were related to each other for the CD38+ B‐CLL cells. On the same cells, CD5 was more selectively expressed on the cell membrane; however, the expression patterns suggested that the cell membrane of CD38− B‐CLL cells contained the least expression level of CD19. Microsc. Res. Tech. 76:1147–1153, 2013 . © 2013 Wiley Periodicals, Inc.