-
Je něco špatně v tomto záznamu ?
Distinct Immunoregulatory Mechanisms in Mesenchymal Stem Cells: Role of the Cytokine Environment
V. Holan, B. Hermankova, P. Bohacova, J. Kossl, M. Chudickova, M. Hajkova, M. Krulova, A. Zajicova, E. Javorkova,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- aktivace lymfocytů účinky léků imunologie MeSH
- antigeny CD279 genetika imunologie metabolismus MeSH
- buněčné mikroprostředí účinky léků imunologie MeSH
- cyklooxygenasa 2 genetika imunologie metabolismus MeSH
- cytokiny imunologie metabolismus farmakologie MeSH
- ELISA MeSH
- exprese genu účinky léků genetika imunologie MeSH
- indolamin-2,3,-dioxygenasa genetika imunologie metabolismus MeSH
- interferon gama farmakologie MeSH
- interleukin-10 imunologie metabolismus MeSH
- interleukin-4 farmakologie MeSH
- interleukin-6 genetika imunologie metabolismus MeSH
- kokultivační techniky MeSH
- kultivované buňky MeSH
- mezenchymální kmenové buňky účinky léků imunologie metabolismus MeSH
- myši MeSH
- polymerázová řetězová reakce s reverzní transkripcí MeSH
- regulační B-lymfocyty účinky léků imunologie metabolismus MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Mesenchymal stem cells (MSCs) represent a population of cells which have the ability to regulate reactivity of T and B lymphocytes by multiple mechanisms. The immunoregulatory activities of MSCs are strictly influenced by the cytokine environment. Here we show that two functionally distinct cytokines, interleukin-4 (IL-4) and interferon-γ (IFN-γ), significantly potentiate the ability of MSCs to inhibit IL-10 production by activated regulatory B cells (Bregs). However, MSCs in the presence of IL-4 or IFN-γ inhibit the IL-10 production by different mechanisms. Preincubation of MSCs with IFN-γ led to the suppression, but pretreatment with IL-4 of neither MSCs nor B cells resulted in the suppression of IL-10 production. The search for candidate regulatory molecules expressed in cytokine-treated MSCs revealed different patterns of the gene expression. Pretreatment of MSCs with IFN-γ, but not with IL-4, induced expression of indoleamine-2,3-dioxygenase, cyclooxygenase-2 and programmed cell death-ligand 1. To identify the molecule(s) responsible for the suppression of IL-10 production, we used specific inhibitors of the putative regulatory molecules. We found that indomethacine, an inhibitor of cyclooxygenase-2 (Cox-2) activity, completely abrogated the inhibition of IL-10 production in cultures containing MSCs and IFN-γ, but had no effect on the suppression in cell cultures containing MSCs and IL-4. The results show that MSCs can inhibit the response of B cells to one stimulus by different mechanisms in dependence on the cytokine environment and thus support the idea of the complexity of immunoregulatory action of MSCs.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc18017023
- 003
- CZ-PrNML
- 005
- 20180518142021.0
- 007
- ta
- 008
- 180515s2016 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1007/s12015-016-9688-y $2 doi
- 035 __
- $a (PubMed)27665290
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Holan, Vladimir $u Department of Transplantation Immunology, Institute of Experimental Medicine, Czech Academy of Sciences, Prague, Videnska 1083, 14220, Prague 4, Czech Republic. holan@biomed.cas.cz. Department of Cell Biology, Faculty of Natural Science, Charles University, Vinicna 7, 12843, Prague 4, Czech Republic. holan@biomed.cas.cz.
- 245 10
- $a Distinct Immunoregulatory Mechanisms in Mesenchymal Stem Cells: Role of the Cytokine Environment / $c V. Holan, B. Hermankova, P. Bohacova, J. Kossl, M. Chudickova, M. Hajkova, M. Krulova, A. Zajicova, E. Javorkova,
- 520 9_
- $a Mesenchymal stem cells (MSCs) represent a population of cells which have the ability to regulate reactivity of T and B lymphocytes by multiple mechanisms. The immunoregulatory activities of MSCs are strictly influenced by the cytokine environment. Here we show that two functionally distinct cytokines, interleukin-4 (IL-4) and interferon-γ (IFN-γ), significantly potentiate the ability of MSCs to inhibit IL-10 production by activated regulatory B cells (Bregs). However, MSCs in the presence of IL-4 or IFN-γ inhibit the IL-10 production by different mechanisms. Preincubation of MSCs with IFN-γ led to the suppression, but pretreatment with IL-4 of neither MSCs nor B cells resulted in the suppression of IL-10 production. The search for candidate regulatory molecules expressed in cytokine-treated MSCs revealed different patterns of the gene expression. Pretreatment of MSCs with IFN-γ, but not with IL-4, induced expression of indoleamine-2,3-dioxygenase, cyclooxygenase-2 and programmed cell death-ligand 1. To identify the molecule(s) responsible for the suppression of IL-10 production, we used specific inhibitors of the putative regulatory molecules. We found that indomethacine, an inhibitor of cyclooxygenase-2 (Cox-2) activity, completely abrogated the inhibition of IL-10 production in cultures containing MSCs and IFN-γ, but had no effect on the suppression in cell cultures containing MSCs and IL-4. The results show that MSCs can inhibit the response of B cells to one stimulus by different mechanisms in dependence on the cytokine environment and thus support the idea of the complexity of immunoregulatory action of MSCs.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a regulační B-lymfocyty $x účinky léků $x imunologie $x metabolismus $7 D060151
- 650 _2
- $a kultivované buňky $7 D002478
- 650 _2
- $a buněčné mikroprostředí $x účinky léků $x imunologie $7 D060833
- 650 _2
- $a kokultivační techniky $7 D018920
- 650 _2
- $a cyklooxygenasa 2 $x genetika $x imunologie $x metabolismus $7 D051546
- 650 _2
- $a cytokiny $x imunologie $x metabolismus $x farmakologie $7 D016207
- 650 _2
- $a ELISA $7 D004797
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a exprese genu $x účinky léků $x genetika $x imunologie $7 D015870
- 650 _2
- $a indolamin-2,3,-dioxygenasa $x genetika $x imunologie $x metabolismus $7 D050503
- 650 _2
- $a interferon gama $x farmakologie $7 D007371
- 650 _2
- $a interleukin-10 $x imunologie $x metabolismus $7 D016753
- 650 _2
- $a interleukin-4 $x farmakologie $7 D015847
- 650 _2
- $a interleukin-6 $x genetika $x imunologie $x metabolismus $7 D015850
- 650 _2
- $a aktivace lymfocytů $x účinky léků $x imunologie $7 D008213
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a mezenchymální kmenové buňky $x účinky léků $x imunologie $x metabolismus $7 D059630
- 650 _2
- $a myši $7 D051379
- 650 _2
- $a antigeny CD279 $x genetika $x imunologie $x metabolismus $7 D061026
- 650 _2
- $a polymerázová řetězová reakce s reverzní transkripcí $7 D020133
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Hermankova, Barbora $u Department of Transplantation Immunology, Institute of Experimental Medicine, Czech Academy of Sciences, Prague, Videnska 1083, 14220, Prague 4, Czech Republic. Department of Cell Biology, Faculty of Natural Science, Charles University, Vinicna 7, 12843, Prague 4, Czech Republic.
- 700 1_
- $a Bohacova, Pavla $u Department of Transplantation Immunology, Institute of Experimental Medicine, Czech Academy of Sciences, Prague, Videnska 1083, 14220, Prague 4, Czech Republic. Department of Cell Biology, Faculty of Natural Science, Charles University, Vinicna 7, 12843, Prague 4, Czech Republic.
- 700 1_
- $a Kossl, Jan $u Department of Transplantation Immunology, Institute of Experimental Medicine, Czech Academy of Sciences, Prague, Videnska 1083, 14220, Prague 4, Czech Republic. Department of Cell Biology, Faculty of Natural Science, Charles University, Vinicna 7, 12843, Prague 4, Czech Republic.
- 700 1_
- $a Chudickova, Milada $u Department of Transplantation Immunology, Institute of Experimental Medicine, Czech Academy of Sciences, Prague, Videnska 1083, 14220, Prague 4, Czech Republic. Department of Cell Biology, Faculty of Natural Science, Charles University, Vinicna 7, 12843, Prague 4, Czech Republic.
- 700 1_
- $a Hajkova, Michaela $u Department of Transplantation Immunology, Institute of Experimental Medicine, Czech Academy of Sciences, Prague, Videnska 1083, 14220, Prague 4, Czech Republic. Department of Cell Biology, Faculty of Natural Science, Charles University, Vinicna 7, 12843, Prague 4, Czech Republic.
- 700 1_
- $a Krulova, Magdalena $u Department of Transplantation Immunology, Institute of Experimental Medicine, Czech Academy of Sciences, Prague, Videnska 1083, 14220, Prague 4, Czech Republic. Department of Cell Biology, Faculty of Natural Science, Charles University, Vinicna 7, 12843, Prague 4, Czech Republic.
- 700 1_
- $a Zajicova, Alena $u Department of Transplantation Immunology, Institute of Experimental Medicine, Czech Academy of Sciences, Prague, Videnska 1083, 14220, Prague 4, Czech Republic.
- 700 1_
- $a Javorkova, Eliska $u Department of Transplantation Immunology, Institute of Experimental Medicine, Czech Academy of Sciences, Prague, Videnska 1083, 14220, Prague 4, Czech Republic. Department of Cell Biology, Faculty of Natural Science, Charles University, Vinicna 7, 12843, Prague 4, Czech Republic.
- 773 0_
- $w MED00184570 $t Stem cell reviews $x 1558-6804 $g Roč. 12, č. 6 (2016), s. 654-663
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/27665290 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20180515 $b ABA008
- 991 __
- $a 20180518142159 $b ABA008
- 999 __
- $a ok $b bmc $g 1300647 $s 1013863
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2016 $b 12 $c 6 $d 654-663 $i 1558-6804 $m Stem cell reviews $n Stem cell rev. $x MED00184570
- LZP __
- $a Pubmed-20180515