-
Je něco špatně v tomto záznamu ?
The Immunological Epigenetic Landscape of the Human Life Trajectory
I. Juříčková, M. Hudec, F. Votava, J. Vosáhlo, SV. Ovsepian, M. Černá, VB. O'Leary
Status neindexováno Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články
NLK
Directory of Open Access Journals
od 2013
PubMed Central
od 2013
Europe PubMed Central
od 2013
ProQuest Central
od 2013-01-01
Open Access Digital Library
od 2013-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2013
- Publikační typ
- časopisecké články MeSH
Adaptive immunity changes over an individual's lifetime, maturing by adulthood and diminishing with old age. Epigenetic mechanisms involving DNA and histone methylation form the molecular basis of immunological memory during lymphocyte development. Monocytes alter their function to convey immune tolerance, yet the epigenetic influences at play remain to be fully understood in the context of lifespan. This study of a healthy genetically homogenous cohort of children, adults and seniors sought to decipher the epigenetic dynamics in B-lymphocytes and monocytes. Variable global cytosine methylation within retro-transposable LINE-1 repeats was noted in monocytes compared to B-lymphocytes across age groups. The expression of the human leukocyte antigen (HLA)-DQ alpha chain gene HLA-DQA1*01 revealed significantly reduced levels in monocytes in all ages relative to B-lymphocytes, as well as between lifespan groups. High melting point analysis and bisulfite sequencing of the HLA-DQA1*01 promoter in monocytes highlighted variable cytosine methylation in children and seniors but greater stability at this locus in adults. Further epigenetic evaluation revealed higher histone lysine 27 trimethylation in monocytes from this adult group. Chromatin immunoprecipitation and RNA pulldown demonstrated association with a novel lncRNA TINA with structurally conserved similarities to the previously recognized epigenetic modifier PARTICLE. Seeking to interpret the epigenetic immunological landscape across three representative age groups, this study focused on HLA-DQA1*01 to expose cytosine and histone methylation alterations and their association with the non-coding transcriptome. Such insights unveil previously unknown complex epigenetic layers, orchestrating the strength and weakening of adaptive immunity with the progression of life.
Faculty of Engineering and Science University of Greenwich London Chatham Maritime Kent ME4 4TB UK
Královské Vinohrady University Hospital Vinohrady 10034 Prague Czech Republic
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc22031301
- 003
- CZ-PrNML
- 005
- 20230127131123.0
- 007
- ta
- 008
- 230119s2022 sz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.3390/biomedicines10112894 $2 doi
- 035 __
- $a (PubMed)36428462
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a sz
- 100 1_
- $a Juříčková, Iva $u Department of Medical Genetics, Third Faculty of Medicine, Charles University, Vinohrady, 10000 Prague, Czech Republic
- 245 14
- $a The Immunological Epigenetic Landscape of the Human Life Trajectory / $c I. Juříčková, M. Hudec, F. Votava, J. Vosáhlo, SV. Ovsepian, M. Černá, VB. O'Leary
- 520 9_
- $a Adaptive immunity changes over an individual's lifetime, maturing by adulthood and diminishing with old age. Epigenetic mechanisms involving DNA and histone methylation form the molecular basis of immunological memory during lymphocyte development. Monocytes alter their function to convey immune tolerance, yet the epigenetic influences at play remain to be fully understood in the context of lifespan. This study of a healthy genetically homogenous cohort of children, adults and seniors sought to decipher the epigenetic dynamics in B-lymphocytes and monocytes. Variable global cytosine methylation within retro-transposable LINE-1 repeats was noted in monocytes compared to B-lymphocytes across age groups. The expression of the human leukocyte antigen (HLA)-DQ alpha chain gene HLA-DQA1*01 revealed significantly reduced levels in monocytes in all ages relative to B-lymphocytes, as well as between lifespan groups. High melting point analysis and bisulfite sequencing of the HLA-DQA1*01 promoter in monocytes highlighted variable cytosine methylation in children and seniors but greater stability at this locus in adults. Further epigenetic evaluation revealed higher histone lysine 27 trimethylation in monocytes from this adult group. Chromatin immunoprecipitation and RNA pulldown demonstrated association with a novel lncRNA TINA with structurally conserved similarities to the previously recognized epigenetic modifier PARTICLE. Seeking to interpret the epigenetic immunological landscape across three representative age groups, this study focused on HLA-DQA1*01 to expose cytosine and histone methylation alterations and their association with the non-coding transcriptome. Such insights unveil previously unknown complex epigenetic layers, orchestrating the strength and weakening of adaptive immunity with the progression of life.
- 590 __
- $a NEINDEXOVÁNO
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Hudec, Michael $u Department of Medical Genetics, Third Faculty of Medicine, Charles University, Vinohrady, 10000 Prague, Czech Republic $1 https://orcid.org/0000000265939911
- 700 1_
- $a Votava, Felix $u Department of Children and Adolescents, Third Faculty of Medicine, Charles University, Vinohrady, 10000 Prague, Czech Republic $u Královské Vinohrady University Hospital, Vinohrady, 10034 Prague, Czech Republic
- 700 1_
- $a Vosáhlo, Jan $u Department of Children and Adolescents, Third Faculty of Medicine, Charles University, Vinohrady, 10000 Prague, Czech Republic $u Královské Vinohrady University Hospital, Vinohrady, 10034 Prague, Czech Republic
- 700 1_
- $a Ovsepian, Saak Victor $u Faculty of Engineering and Science, University of Greenwich London, Chatham Maritime, Kent ME4 4TB, UK
- 700 1_
- $a Černá, Marie $u Department of Medical Genetics, Third Faculty of Medicine, Charles University, Vinohrady, 10000 Prague, Czech Republic $1 https://orcid.org/0000000212085588
- 700 1_
- $a O'Leary, Valerie Bríd $u Department of Medical Genetics, Third Faculty of Medicine, Charles University, Vinohrady, 10000 Prague, Czech Republic $1 https://orcid.org/0000000311719830
- 773 0_
- $w MED00205373 $t Biomedicines $x 2227-9059 $g Roč. 10, č. 11 (2022)
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/36428462 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20230119 $b ABA008
- 991 __
- $a 20230127131115 $b ABA008
- 999 __
- $a ok $b bmc $g 1889448 $s 1182634
- BAS __
- $a 3
- BAS __
- $a PreBMC-PubMed-not-MEDLINE
- BMC __
- $a 2022 $b 10 $c 11 $e 20221111 $i 2227-9059 $m Biomedicines $n Biomedicines $x MED00205373
- LZP __
- $a Pubmed-20230119