Detail
Článek
Článek online
FT
Medvik - BMČ
  • Je něco špatně v tomto záznamu ?

Comparison of two human organoid models of lung and intestinal inflammation reveals Toll-like receptor signalling activation and monocyte recruitment

SS. Jose, M. De Zuani, F. Tidu, M. Hortová Kohoutková, L. Pazzagli, G. Forte, R. Spaccapelo, T. Zelante, J. Frič,

. 2020 ; 9 (5) : e1131. [pub] 20200505

Jazyk angličtina Země Austrálie

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc20019232

Objectives: The activation of immune responses in mucosal tissues is a key factor for the development and sustainment of several pathologies including infectious diseases and autoimmune diseases. However, translational research and personalised medicine struggle to advance because of the lack of suitable preclinical models that successfully mimic the complexity of human tissues without relying on in vivo mouse models. Here, we propose two in vitro human 3D tissue models, deprived of any resident leucocytes, to model mucosal tissue inflammatory processes. Methods: We developed human 3D lung and intestinal organoids differentiated from induced pluripotent stem cells to model mucosal tissues. We then compared their response to a panel of microbial ligands and investigated their ability to attract and host human primary monocytes. Results: Mature lung and intestinal organoids comprised epithelial (EpCAM+) and mesenchymal (CD73+) cells which responded to Toll-like receptor stimulation by releasing pro-inflammatory cytokines and expressing tissue inflammatory markers including MMP9, COX2 and CRP. When added to the organoid culture, primary human monocytes migrated towards the organoids and began to differentiate to an 'intermediate-like' phenotype characterised by increased levels of CD14 and CD16. Conclusion: We show that human mucosal organoids exhibit proper immune functions and successfully mimic an immunocompetent tissue microenvironment able to host patient-derived immune cells. Our experimental set-up provides a novel tool to tackle the complexity of immune responses in mucosal tissues which can be tailored to different human pathologies.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc20019232
003      
CZ-PrNML
005      
20201123123829.0
007      
ta
008      
201103s2020 at f 000 0|eng||
009      
AR
024    7_
$a 10.1002/cti2.1131 $2 doi
035    __
$a (PubMed)32377340
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a at
100    1_
$a Jose, Shyam Sushama $u International Clinical Research Center St. Anne's University Hospital Brno Brno Czech Republic.
245    10
$a Comparison of two human organoid models of lung and intestinal inflammation reveals Toll-like receptor signalling activation and monocyte recruitment / $c SS. Jose, M. De Zuani, F. Tidu, M. Hortová Kohoutková, L. Pazzagli, G. Forte, R. Spaccapelo, T. Zelante, J. Frič,
520    9_
$a Objectives: The activation of immune responses in mucosal tissues is a key factor for the development and sustainment of several pathologies including infectious diseases and autoimmune diseases. However, translational research and personalised medicine struggle to advance because of the lack of suitable preclinical models that successfully mimic the complexity of human tissues without relying on in vivo mouse models. Here, we propose two in vitro human 3D tissue models, deprived of any resident leucocytes, to model mucosal tissue inflammatory processes. Methods: We developed human 3D lung and intestinal organoids differentiated from induced pluripotent stem cells to model mucosal tissues. We then compared their response to a panel of microbial ligands and investigated their ability to attract and host human primary monocytes. Results: Mature lung and intestinal organoids comprised epithelial (EpCAM+) and mesenchymal (CD73+) cells which responded to Toll-like receptor stimulation by releasing pro-inflammatory cytokines and expressing tissue inflammatory markers including MMP9, COX2 and CRP. When added to the organoid culture, primary human monocytes migrated towards the organoids and began to differentiate to an 'intermediate-like' phenotype characterised by increased levels of CD14 and CD16. Conclusion: We show that human mucosal organoids exhibit proper immune functions and successfully mimic an immunocompetent tissue microenvironment able to host patient-derived immune cells. Our experimental set-up provides a novel tool to tackle the complexity of immune responses in mucosal tissues which can be tailored to different human pathologies.
655    _2
$a časopisecké články $7 D016428
700    1_
$a De Zuani, Marco $u International Clinical Research Center St. Anne's University Hospital Brno Brno Czech Republic.
700    1_
$a Tidu, Federico $u International Clinical Research Center St. Anne's University Hospital Brno Brno Czech Republic. Department of Biology Faculty of Medicine Masaryk University Brno Czech Republic.
700    1_
$a Hortová Kohoutková, Marcela $u International Clinical Research Center St. Anne's University Hospital Brno Brno Czech Republic.
700    1_
$a Pazzagli, Lucia $u Department of Experimental Medicine and University Research Center for Functional Genomic (C.U.R.Ge.F) University of Perugia Perugia Italy.
700    1_
$a Forte, Giancarlo $u International Clinical Research Center St. Anne's University Hospital Brno Brno Czech Republic.
700    1_
$a Spaccapelo, Roberta $u Department of Experimental Medicine and University Research Center for Functional Genomic (C.U.R.Ge.F) University of Perugia Perugia Italy.
700    1_
$a Zelante, Teresa $u Department of Experimental Medicine and University Research Center for Functional Genomic (C.U.R.Ge.F) University of Perugia Perugia Italy.
700    1_
$a Frič, Jan $u International Clinical Research Center St. Anne's University Hospital Brno Brno Czech Republic. Institute of Hematology and Blood Transfusion Prague Czech Republic.
773    0_
$w MED00205362 $t Clinical & translational immunology $x 2050-0068 $g Roč. 9, č. 5 (2020), s. e1131
856    41
$u https://pubmed.ncbi.nlm.nih.gov/32377340 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20201103 $b ABA008
991    __
$a 20201123123828 $b ABA008
999    __
$a ind $b bmc $g 1586012 $s 1109430
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2020 $b 9 $c 5 $d e1131 $e 20200505 $i 2050-0068 $m Clinical & translational immunology $n Clin Transl Immunology $x MED00205362
LZP    __
$a Pubmed-20201103

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...