A novel approach to the measurement of different in vitro leukaemic cell growth parameters: the use of PKH GL fluorescent probes
- PMID: 7692186
- DOI: 10.1016/0145-2126(93)90153-c
A novel approach to the measurement of different in vitro leukaemic cell growth parameters: the use of PKH GL fluorescent probes
Abstract
The application of the fluorescent cell membrane probes PKH2 and PKH 26 GL in the measurement of leukaemic cell growth was examined on four cell lines K562, NALM-6, ACV (a pre-B cell line) and HL-60 using flow cytometry. As the amount of probe per cell reduces at each cell division, the fluorescence can be used to measure cell proliferation. By measuring the mean fluorescence intensity of the cells at the beginning of culture and at various time points, and by combining this information with a viable cell count, it was possible to determine: (1) the number of viable cells; (2) their rate of proliferation; (3) their number of cell divisions; and (4) the maintenance of cells in a viable state over a period of time. It was demonstrated that these parameters could be reliably established using the red fluorescent probe PKH26 GL. In contrast, the green fluorescent probe PKH2 GL showed dye transfer resulting in an underestimation of the number of cell divisions and an overestimation of the maintenance of cells in a viable state. The potential advantages of the use of PKH26 GL over conventional assays for the measurement of leukaemic cell growth parameters are discussed.
Similar articles
-
Measurement of the growth parameters of precursor B-acute lymphoblastic leukaemic cells in co-culture with bone marrow stromal cells; detection of two cd10 positive populations with different proliferative capacities and survival.Leuk Res. 1994 Jan;18(1):37-48. doi: 10.1016/0145-2126(94)90007-8. Leuk Res. 1994. PMID: 8289465
-
Phototoxicity of the fluorescent membrane dyes PKH2 and PKH26 on the human hematopoietic KG1a progenitor cell line.Cytometry. 1999 Aug 1;36(4):312-8. doi: 10.1002/(sici)1097-0320(19990801)36:4<312::aid-cyto5>3.0.co;2-v. Cytometry. 1999. PMID: 10404146
-
PKH26 probe in the study of the proliferation of chemoresistant leukemic sublines.Anticancer Res. 1998 Nov-Dec;18(6A):4243-51. Anticancer Res. 1998. PMID: 9891474
-
Fluorescent dyes for lymphocyte migration and proliferation studies.Immunol Cell Biol. 1999 Dec;77(6):499-508. doi: 10.1046/j.1440-1711.1999.00877.x. Immunol Cell Biol. 1999. PMID: 10571670 Review.
-
Monitoring Cell Proliferation by Dye Dilution: Considerations for Panel Design.Methods Mol Biol. 2024;2779:159-216. doi: 10.1007/978-1-0716-3738-8_9. Methods Mol Biol. 2024. PMID: 38526787 Review.
Cited by
-
Late-stage immature neocortical neurons reconstruct interhemispheric connections and form synaptic contacts with increased efficiency in adult mouse cortex undergoing targeted neurodegeneration.J Neurosci. 2002 May 15;22(10):4045-56. doi: 10.1523/JNEUROSCI.22-10-04045.2002. J Neurosci. 2002. PMID: 12019324 Free PMC article.
-
Methods to Assess Proliferation of Stimulated Human Lymphocytes In Vitro: A Narrative Review.Cells. 2023 Jan 20;12(3):386. doi: 10.3390/cells12030386. Cells. 2023. PMID: 36766728 Free PMC article. Review.
-
From seeing to believing: labelling strategies for in vivo cell-tracking experiments.Interface Focus. 2013 Jun 6;3(3):20130001. doi: 10.1098/rsfs.2013.0001. Interface Focus. 2013. PMID: 23853708 Free PMC article.
-
Nucleofection induces non-specific changes in the metabolic activity of transfected cells.Mol Biol Rep. 2012 Mar;39(3):2187-94. doi: 10.1007/s11033-011-0967-z. Epub 2011 Jun 5. Mol Biol Rep. 2012. PMID: 21643953 Free PMC article.
-
Tracking chondrocytes and assessing their proliferation with carboxyfluorescein diacetate succinimidyl ester: effects on cell functions.Tissue Eng Part C Methods. 2010 Apr;16(2):301-10. doi: 10.1089/ten.TEC.2008.0609. Tissue Eng Part C Methods. 2010. PMID: 19558220 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Medical
Research Materials