Flow cytometric measurement of absolute telomere length
- Authors: Demina I.A.1, Semchenkova A.A.2, Kagirova Z.R.3, Popov A.M.2
-
Affiliations:
- Dmitriy Rogachev National Medical Research Center of Pediatric Hematology, Oncology, Immunology Ministry of Healthcare of Russian Federation
- Dmitriy Rogachev National Medical Research Center of Pediatric Hematology, Oncology, Immunology Ministry of Healthcare of Russian Federation.
- Russian National Research Medical University named after N.I. Pirogov.
- Issue: Vol 17, No 4 (2018)
- Pages: 68-74
- Section: CLINICAL SIGNIFICANCE OF BASIC RESEARCH
- Submitted: 12.01.2019
- Accepted: 12.01.2019
- Published: 12.01.2019
- URL: https://hemoncim.com/jour/article/view/216
- DOI: https://doi.org/10.24287/1726-1708-2018-17-4-68-74
- ID: 216
Cite item
Full Text
Abstract
The length of the end of chromosomes – telomeres is a dynamic and constant characterizes cellular aging process. Measurement of telomere length (TL) and its connection with the diagnosis, course, prognosis and treatment of a number of diseases in recent years, is of great interest for researchers. The methods used for this are varied and are primarily by molecular biological. Variability of methodological approaches, the lack of a common standard of measurement TL measurements in absolute and relative terms: all this leads to results that cannot be compared with each other. The aim of this work is the development of data conversion algorithm is obtained by flow cytometry in absolute telomere length, expressed in kilobases (kb). The study was conducted from venous blood of children 2–3 years of age (8 healthy children and 3 patients with dyskeratosis congenita). As control material used cell line 1301 (ATCC, UK). Determination of relative telomere length was performed by using a set FlowFISH Telomere PNA Kit / FITC (DakoCytomation, Glostrup, Denmark). RTL code and the absolute length of telomeres were calculated for each study participant. Data on the length of patients telomere were compared with data on TL healthy children of appropriate age. RTL average value for healthy children 2–3 years was 30.1, and an absolute telomere length – 15.56 kb. Telomere length patients with dyskeratosis congenita was significantly shorter (RTL 1.4–4.3, the absolute value of TL 0.3–2.4 kb). The algorithm conversion molecular fluorescence equivalent in absolute TL is universal and can be used in any laboratory equipped with a flow cytometer. The resulting data TL can be compared with the data expressed in absolute units and obtained by any other method.
Keywords
About the authors
I. A. Demina
Dmitriy Rogachev National Medical Research Center of Pediatric Hematology, Oncology, Immunology Ministry of Healthcare of Russian Federation
Author for correspondence.
Email: idemina@mail.ru
ORCID iD: 0000-0002-4317-2094
PhD, leading scientist Laboratory of cell’s immunology and immunogenesis.
117997, Moscow, Samory Mashela st., 1.
Russian Federation
A. A. Semchenkova
Dmitriy Rogachev National Medical Research Center of Pediatric Hematology, Oncology, Immunology Ministry of Healthcare of Russian Federation.
ORCID iD: 0000-0002-7082-1694
Russian Federation
Z. R. Kagirova
Russian National Research Medical University named after N.I. Pirogov.
ORCID iD: 0000-0001-9002-7909
Russian Federation
A. M. Popov
Dmitriy Rogachev National Medical Research Center of Pediatric Hematology, Oncology, Immunology Ministry of Healthcare of Russian Federation.
ORCID iD: 0000-0002-0889-6986
Russian Federation
References
- de Lange T. Shelterin: the protein complex that shapes and safeguards human telomeres. Genes & development 2005; 19 (18): 2100–10.
- Callen E., Surralles J. Telomere dysfunction in genome instability syndromes. Mutation research 2004; 567 (1): 85–104.
- Jang J.S., Choi Y.Y., Lee W.K., Choi J.E., Cha S.I., Kim Y.J., et al. Telomere length and the risk of lung cancer. Cancer science 2008; 99 (7): 1385–9.
- Plentz R.R., Wiemann S.U., Flemming P., Meier P.N., Kubicka S., Kreipe H., et al. Telomere shortening of epithelial cells characterises the adenoma-carcinoma transition of human colorectal cancer. Gut 2003; 52 (9): 1304–7.
- Sieglova Z., Zilovcova S., Cermak J., Rihova H., Brezinova D., Dvorakova R., et al. Dynamics of telomere erosion and its association with genome instability in myelodysplastic syndromes (MDS) and acute myelogenous leukemia arising from MDS: a marker of disease prognosis? Leukemia research 2004; 28 (10): 1013–21.
- Epel E.S., Blackburn E.H., Lin J., Dhab- har F.S., Adler N.E., Morrow J.D., Cawthon R.M. Accelerated telomere shortening in response to life stress. PNAS 2004; 101 (49):17312–5.
- Morla M., Busquets X., Pons J., Saule- da J., MacNee W., Agusti A.G. Telomere shortening in smokers with and without COPD. Eur Respir J 2006; 27 (3): 525–8.
- Paul L., Cattaneo M., D’Angelo A., Sampietro F., Fermo I., Razzari C., et al. Telomere length in peripheral blood mononuclear cells is associated with folate status in men. J Nutrit 2009; 139 (7): 1273–8.
- Zannolli R., Mohn A., Buoni S., Pietro- belli A., Messina M., Chiarelli F., Miracco C. Telomere length and obesity. Acta Paediatr 2008; 97 (7): 952–4.
- Stefa A., Lamprokostopoulou A., Bria- na D.D., Kontogeorgou A., Papageorgiou I., Malamitsi-Puchner A., et al. The effect of intrauterine growth on leukocyte telomere length at birth. J Matern Fetal Neonatal Med 2018. doi: 10.1080/14767058.2018.1479392
- Bakaysa S.L., Mucci L.A., Slagbo- om P.E., Boomsma D.I., McClearn G.E., Johansson B., Pedersen N.L. Telomere length predicts survival independent of genetic influences. Aging cell 2007: 6 (6): 769–74.
- Baerlocher G.M., Vulto I., de Jong G., Lansdorp P.M. Flow cytometry and FISH to measure the average length of telomeres (flow FISH). Nat Protoc 2006; 1 (5): 2365–76.
- Hultdin M., Gronlund E., Norrback K., Eriksson-Lindström E., Just T., Roos G. Telomere analysis by fluorescence in situ hybridization and flow cytometry. Nucleic Acids Res 1998; 26 (16): 3651–6.
- O’Callaghan N.J., O’Callaghan M.F. A quantitative PCR method for measuring absolute telomere length. Biol Proced Online 2011; 13: 3. doi: 10.1186/1480-9222-13-3
- Mitchell J.R., Wood E., Collins K. A telomerase component is defective in the human disease dyskeratosis congenita. Nature 1999; 402 (6761): 551–5.
- Alter B.P., Giri N., Savage S.A., Rosen- berg P.S. Telomere length in inherited bone marrow failure syndromes. Haematologica 2015; 100 (1): 49–54.
- Britt-Compton B., Rowson J., Loc- ke M., Mackenzie I., Kipling D., Baird D.M. Structural stability and chromosomespecific telomere length is governed by cis-acting determinants in humans. Hum Mol Genet 2006; 15 (5): 725–33.
- Baird D.M., Rowson J., Wynford-Tho- mas D., Kipling D. Extensive allelic variation and ultrashort telomeres in senescent human cells. Nat Genet 2003; 33 (2): 203–7.
- Njajou O.T., Hsueh W.C., Blackburn E.H., Newman A.B., Wu S.H., Li R., et al. Association between telomere length, specific causes of death, and years of healthy life in health, aging, and body composition, a population-based cohort study. J Gerontol A Biol Sci Med Sci 2009; 64 (8): 860–4.
- Poon S.S., Lansdorp P.M. Measurements of telomere length on individual chromosomes by image cytometry. Methods Cell Biol 2001; 64 (part B): 69–96.
- Canela A., Vera E., Klatt P., Blas- co M.A. High-throughput telomere length quantification by FISH and its application to human population studies. PNAS 2007; 104 (13): 5300–5.
- Gutierrez-Rodrigues F., Santana- Lemos B.A., Scheucher P.S., Alves- Paiva R.M., Calado R.T. Direct comparison of Flow-FISH and qPCR as diagnostic tests for telomere length measurement in humans. PLOS ONE 2014; 9 (11): e113747. doi: 10.1371/journal.pone.0113747
Supplementary files
