Collapse of Telomere Homeostasis in Hematopoietic Cells Caused by Heterozygous Mutations in Telomerase Genes
Telomerase activity is readily detectable in extracts from human hematopoietic stem and progenitor cells, but appears unable to maintain telomere length with proliferation in vitro and with age in vivo. We performed a detailed study of the telomere length by flow FISH analysis in leukocytes from 835 healthy individuals and 60 individuals with reduced telomerase activity. Healthy individuals showed a broad range in average telomere length in granulocytes and lymphocytes at any given age. The average telomere length declined with age at a rate that differed between age-specific breakpoints and between cell types. Gender differences between leukocyte telomere lengths were observed for all cell subsets studied; interestingly, this trend could already be detected at birth. Heterozygous carriers for mutations in either the telomerase reverse transcriptase (hTERT) or the telomerase RNA template (hTERC) gene displayed striking and comparable telomere length deficits. Further, non-carrier relatives of such heterozygous individuals had somewhat shorter leukocyte telomere lengths than expected; this difference was most profound for granulocytes. Failure to maintain telomere homeostasis as a result of partial telomerase deficiency is thought to trigger cell senescence or cell death, eventually causing tissue failure syndromes. Our data are consistent with these statements and suggest that the likelihood of similar processes occurring in normal individuals increases with age. Our work highlights the essential role of telomerase in the hematopoietic system and supports the notion that telomerase levels in hematopoietic cells, while limiting and unable to prevent overall telomere shortening, are nevertheless crucial to maintain telomere homeostasis with age.
Vyšlo v časopise:
Collapse of Telomere Homeostasis in Hematopoietic Cells Caused by Heterozygous Mutations in Telomerase Genes. PLoS Genet 8(5): e32767. doi:10.1371/journal.pgen.1002696
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.pgen.1002696
Souhrn
Telomerase activity is readily detectable in extracts from human hematopoietic stem and progenitor cells, but appears unable to maintain telomere length with proliferation in vitro and with age in vivo. We performed a detailed study of the telomere length by flow FISH analysis in leukocytes from 835 healthy individuals and 60 individuals with reduced telomerase activity. Healthy individuals showed a broad range in average telomere length in granulocytes and lymphocytes at any given age. The average telomere length declined with age at a rate that differed between age-specific breakpoints and between cell types. Gender differences between leukocyte telomere lengths were observed for all cell subsets studied; interestingly, this trend could already be detected at birth. Heterozygous carriers for mutations in either the telomerase reverse transcriptase (hTERT) or the telomerase RNA template (hTERC) gene displayed striking and comparable telomere length deficits. Further, non-carrier relatives of such heterozygous individuals had somewhat shorter leukocyte telomere lengths than expected; this difference was most profound for granulocytes. Failure to maintain telomere homeostasis as a result of partial telomerase deficiency is thought to trigger cell senescence or cell death, eventually causing tissue failure syndromes. Our data are consistent with these statements and suggest that the likelihood of similar processes occurring in normal individuals increases with age. Our work highlights the essential role of telomerase in the hematopoietic system and supports the notion that telomerase levels in hematopoietic cells, while limiting and unable to prevent overall telomere shortening, are nevertheless crucial to maintain telomere homeostasis with age.
Zdroje
1. d'Adda di FagagnaFReaperPMClay-FarraceLFieglerHCarrP 2003 A DNA damage checkpoint response in telomere-initiated senescence. Nature 426 194 198
2. SmogorzewskaAde LangeT 2002 Different telomere damage signaling pathways in human and mouse cells. Embo J 21 4338 4348
3. Britt-ComptonBRowsonJLockeMMackenzieIKiplingD 2006 Structural stability and chromosome-specific telomere length is governed by cis-acting determinants in humans. Hum Mol Genet 15 725 733
4. GreiderCWBlackburnEH 1985 Identification of a specific telomere terminal transferase activity in Tetrahymena extracts. Cell 43 405 413
5. MuntoniANeumannAAHillsMReddelRR 2009 Telomere elongation involves intra-molecular DNA replication in cells utilizing alternative lengthening of telomeres. Hum Mol Genet 18 1017 1027
6. LansdorpPM 2005 Major cutbacks at chromosome ends. Trends Biochem Sci 30 388 395
7. HemannMTStrongMAHaoLYGreiderCW 2001 The shortest telomere, not average telomere length, is critical for cell viability and chromosome stability. Cell 107 67 77
8. AubertGLansdorpPM 2008 Telomeres and aging. Physiol Rev 88 557 579
9. AubertGHillsMLansdorpPM 2011 Telomere length measurement-Caveats and a critical assessment of the available technologies and tools. Mutat Res 730 59 67
10. LansdorpPMVerwoerdNPvan de RijkeFMDragowskaVLittleMT 1996 Heterogeneity in telomere length of human chromosomes. Hum Mol Genet 5 685 691
11. MartensUMZijlmansJMPoonSSDragowskaWYuiJ 1998 Short telomeres on human chromosome 17p. Nat Genet 18 76 80
12. ChangEHarleyCB 1995 Telomere length and replicative aging in human vascular tissues. Proc Natl Acad Sci U S A 92 11190 11194
13. HastieNDDempsterMDunlopMGThompsonAMGreenDK 1990 Telomere reduction in human colorectal carcinoma and with ageing. Nature 346 866 868
14. RuferNBrummendorfTHKolvraaSBischoffCChristensenK 1999 Telomere fluorescence measurements in granulocytes and T lymphocyte subsets point to a high turnover of hematopoietic stem cells and memory T cells in early childhood. J Exp Med 190 157 167
15. SlagboomPEDroogSBoomsmaDI 1994 Genetic determination of telomere size in humans: a twin study of three age groups. Am J Hum Genet 55 876 882
16. HarleyCBFutcherABGreiderCW 1990 Telomeres shorten during ageing of human fibroblasts. Nature 345 458 460
17. BaerlocherGMMakJRothARiceKSLansdorpPM 2003 Telomere shortening in leukocyte subpopulations from baboons. J Leukoc Biol 73 289 296
18. HillsMLuckeKChavezEAEavesCJLansdorpPM 2009 Probing the mitotic history and developmental stage of hematopoietic cells using single telomere length analysis (STELA). Blood 113 5765 5775
19. VaziriHDragowskaWAllsoppRCThomasTEHarleyCB 1994 Evidence for a mitotic clock in human hematopoietic stem cells: loss of telomeric DNA with age. Proc Natl Acad Sci U S A 91 9857 9860
20. BroccoliDYoungJWde LangeT 1995 Telomerase activity in normal and malignant hematopoietic cells. Proc Natl Acad Sci U S A 92 9082 9086
21. ChiuCPDragowskaWKimNWVaziriHYuiJ 1996 Differential expression of telomerase activity in hematopoietic progenitors from adult human bone marrow. Stem Cells 14 239 248
22. WengNPPalmerLDLevineBLLaneHCJuneCH 1997 Tales of tails: regulation of telomere length and telomerase activity during lymphocyte development, differentiation, activation, and aging. Immunol Rev 160 43 54
23. ShepherdBEGuttorpPLansdorpPMAbkowitzJL 2004 Estimating human hematopoietic stem cell kinetics using granulocyte telomere lengths. Exp Hematol 32 1040 1050
24. CaladoRTYoungNS 2009 Telomere diseases. N Engl J Med 361 2353 2365
25. AlterBPBaerlocherGMSavageSAChanockSJWekslerBB 2007 Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita. Blood 110 1439 1447
26. KirwanMDokalI 2008 Dyskeratosis congenita: a genetic disorder of many faces. Clin Genet 73 103 112
27. ArmaniosMYChenJJCoganJDAlderJKIngersollRG 2007 Telomerase mutations in families with idiopathic pulmonary fibrosis. N Engl J Med 356 1317 1326
28. BaerlocherGMRiceKVultoILansdorpPM 2007 Longitudinal data on telomere length in leukocytes from newborn baboons support a marked drop in stem cell turnover around 1 year of age. Aging Cell 6 121 123
29. JuZJiangHJaworskiMRathinamCGompfA 2007 Telomere dysfunction induces environmental alterations limiting hematopoietic stem cell function and engraftment. Nat Med 13 742 747
30. ParkJIVenteicherASHongJYChoiJJunS 2009 Telomerase modulates Wnt signalling by association with target gene chromatin. Nature 460 66 72
31. XuLBlackburnEH 2007 Human cancer cells harbor T-stumps, a distinct class of extremely short telomeres. Mol Cell 28 315 327
32. TakaiHSmogorzewskaAde LangeT 2003 DNA damage foci at dysfunctional telomeres. Curr Biol 13 1549 1556
33. LansdorpPM 2000 Repair of telomeric DNA prior to replicative senescence. Mech Ageing Dev 118 23 34
34. RheeDBGhoshALuJBohrVALiuY 2011 Factors that influence telomeric oxidative base damage and repair by DNA glycosylase OGG1. DNA Repair (Amst) 10 34 44
35. SahinECollaSLiesaMMoslehiJMullerFL 2011 Telomere dysfunction induces metabolic and mitochondrial compromise. Nature 470 359 365
36. BakerDJWijshakeTTchkoniaTLeBrasseurNKChildsBG 2011 Clearance of p16Ink4a-positive senescent cells delays ageing-associated disorders. Nature 479 232 236
37. VulliamyTJDokalI 2008 Dyskeratosis congenita: the diverse clinical presentation of mutations in the telomerase complex. Biochimie 90 122 130
38. FrenckRWJrBlackburnEHShannonKM 1998 The rate of telomere sequence loss in human leukocytes varies with age. Proc Natl Acad Sci U S A 95 5607 5610
39. LansdorpPMDragowskaWMayaniH 1993 Ontogeny-related changes in proliferative potential of human hematopoietic cells. J Exp Med 178 787 791
40. BowieMBKentDGDykstraBMcKnightKDMcCaffreyL 2007 Identification of a new intrinsically timed developmental checkpoint that reprograms key hematopoietic stem cell properties. Proc Natl Acad Sci U S A 104 5878 5882
41. KimISaundersTLMorrisonSJ 2007 Sox17 dependence distinguishes the transcriptional regulation of fetal from adult hematopoietic stem cells. Cell 130 470 483
42. LansdorpPM 2009 Telomeres and disease. EMBO J 28 2532 2540
43. MocchegianiEMalavoltaM 2004 NK and NKT cell functions in immunosenescence. Aging Cell 3 177 184
44. BuchkovichKJGreiderCW 1996 Telomerase regulation during entry into the cell cycle in normal human T cells. Mol Biol Cell 7 1443 1454
45. GeigerHRudolphKL 2009 Aging in the lympho-hematopoietic stem cell compartment. Trends Immunol 30 360 365
46. KnudsonMKulkarniSBallasZKBesslerMGoldmanF 2005 Association of immune abnormalities with telomere shortening in autosomal-dominant dyskeratosis congenita. Blood 105 682 688
47. BenetosAOkudaKLajemiMKimuraMThomasF 2001 Telomere length as an indicator of biological aging: The gender effect and relation with pulse pressure and pulse wave velocity. Hypertension 37 381 385
48. CaladoRTYewdellWTWilkersonKLRegalJAKajigayaS 2009 Sex hormones, acting on the TERT gene, increase telomerase activity in human primary hematopoietic cells. Blood 114 2236 2243
49. SalpeaKDHumphriesSE 2010 Telomere length in atherosclerosis and diabetes. Atherosclerosis 209 35 38
50. EpelESBlackburnEHLinJDhabharFSAdlerNE 2004 Accelerated telomere shortening in response to life stress. Proc Natl Acad Sci U S A 101 17312 17315
51. CawthonRMSmithKRO'BrienESivatchenkoAKerberRA 2003 Association between telomere length in blood and mortality in people aged 60 years or older. Lancet 361 393 395
52. NjajouOTHsuehWCBlackburnEHNewmanABWuSH 2009 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 64 860 864
53. AlderJKChenJJLancasterLDanoffSSuSC 2008 Short telomeres are a risk factor for idiopathic pulmonary fibrosis. Proc Natl Acad Sci U S A 105 13051 13056
54. CaladoRTRegalJAHillsMYewdellWTDalmazzoLF 2009 Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia. Proc Natl Acad Sci U S A 106 1187 1192
55. CaladoRTRegalJAKajigayaSYoungNS 2009 Erosion of telomeric single-stranded overhang in patients with aplastic anaemia carrying telomerase complex mutations. Eur J Clin Invest 39 1025 1032
56. GoldmanFDAubertGKlingelhutzAJHillsMCooperSR 2008 Characterization of primitive hematopoietic cells from patients with dyskeratosis congenita. Blood 111 4523 4531
57. LyHSchertzerMJastaniahWDavisJYongSL 2005 Identification and functional characterization of two variant alleles of the telomerase RNA template gene (TERC) in a patient with Dyskeratosis Congenita. Blood 106 1246 1252
58. YamaguchiHBaerlocherGMLansdorpPMChanockSJNunezO 2003 Mutations of the human telomerase RNA gene (TERC) in aplastic anemia and myelodysplastic syndrome. Blood 102 916 918
59. YamaguchiHCaladoRTLyHKajigayaSBaerlocherGM 2005 Mutations in TERT, the gene for telomerase reverse transcriptase, in aplastic anemia. N Engl J Med 352 1413 1424
60. TanejaKLChavezEACoullJLansdorpPM 2001 Multicolor fluorescence in situ hybridization with peptide nucleic acid probes for enumeration of specific chromosomes in human cells. Genes Chromosomes Cancer 30 57 63
61. BaerlocherGMVultoIde JongGLansdorpPM 2006 Flow cytometry and FISH to measure the average length of telomeres (flow FISH). Nat Protoc 1 2365 2376
62. Lopez-VergesSMilushJMPandeySYorkVAArakawa-HoytJ 2010 CD57 defines a functionally distinct population of mature NK cells in the human CD56dimCD16+ NK-cell subset. Blood 116 3865 3874
63. BaerlocherGMLansdorpPM 2003 Telomere length measurements in leukocyte subsets by automated multicolor flow-FISH. Cytometry A 55 1 6
64. ChambersJMHastieTJ 1992 Statistical Models in S. Pacific Grove, CA: Wadsworth & Brooks/Cole
Štítky
Genetika Reprodukčná medicínaČlánok vyšiel v časopise
PLOS Genetics
2012 Číslo 5
- Je „freeze-all“ pro všechny? Odborníci na fertilitu diskutovali na virtuálním summitu
- Gynekologové a odborníci na reprodukční medicínu se sejdou na prvním virtuálním summitu
Najčítanejšie v tomto čísle
- Inactivation of a Novel FGF23 Regulator, FAM20C, Leads to Hypophosphatemic Rickets in Mice
- Genome-Wide Association of Pericardial Fat Identifies a Unique Locus for Ectopic Fat
- Slowing Replication in Preparation for Reduction
- Deletion of PTH Rescues Skeletal Abnormalities and High Osteopontin Levels in Mice