Bone Marrow-Derived Mesenchymal Stromal Cells (MSCs) Modulate the Inflammatory Character of Alveolar Macrophages from Sarcoidosis Patients.

alveolar macrophages bone marrow stromal cells cell therapy sarcoidosis

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
19 Jan 2020
Historique:
received: 16 12 2019
revised: 02 01 2020
accepted: 14 01 2020
entrez: 23 1 2020
pubmed: 23 1 2020
medline: 23 1 2020
Statut: epublish

Résumé

Sarcoidosis is a devastating inflammatory disease affecting many organs, especially the lungs and lymph nodes. Bone marrow-derived mesenchymal stromal cells (MSCs) can "reprogram" various types of macrophages towards an anti-inflammatory phenotype. We wanted to determine whether alveolar macrophages from sarcoidosis subjects behave similarly by mounting an anti-inflammatory response when co-cultured with MSCs. Fifteen sarcoidosis and eight control subjects underwent bronchoscopy and bronchoalveolar lavage (BAL). Unselected BAL cells (70-94% macrophages) were isolated and cultured with and without MSCs from healthy adults. Following stimulation of the cultured cells with lipopolysaccharide, the medium was removed to measure interleukin 10 and tumor necrosis factor alpha (IL-10 and TNF-α). In two additional sarcoidosis subjects, flow cytometry was used to study intracellular cytokines and surface markers associated with alveolar macrophages to confirm the results. Unselected BAL cells from sarcoidosis subjects co-cultured with MSCs showed a reduction in TNF-α (pro-inflammatory M1) and an increase in IL-10 (anti-inflammatory M2) in 9 of 11 samples studied. Control subject samples showed few, if any, differences in cytokine production. Unselected BAL cells from two additional patients analyzed by flow cytometry confirmed a switch towards an anti-inflammatory state (i.e., M1 to M2) after co-culture with MSCs. These results suggest that, similarly to other macrophages, alveolar macrophages also respond to MSC contacts by changing towards an anti-inflammatory phenotype. Based on our results, we hypothesize that mesenchymal stromal cells applied to the airways might alleviate lung inflammation and decrease steroid need in patients with sarcoidosis.

Identifiants

pubmed: 31963936
pii: jcm9010278
doi: 10.3390/jcm9010278
pmc: PMC7019909
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : NIH HHS
ID : Intramural Research Program
Pays : United States
Organisme : Semmelweis University Dean's Research Award
ID : 2015

Références

Blood. 2007 Nov 15;110(10):3499-506
pubmed: 17664353
Respir Res. 2018 Apr 18;19(1):66
pubmed: 29669565
Sci Rep. 2016 Dec 02;6:38308
pubmed: 27910911
Expert Opin Biol Ther. 2018 Apr;18(4):399-407
pubmed: 29327613
Blood. 2005 Feb 15;105(4):1815-22
pubmed: 15494428
Sci Transl Med. 2017 Nov 15;9(416):
pubmed: 29141887
Front Immunol. 2019 Jul 31;10:1645
pubmed: 31417542
Mediators Inflamm. 2015;2015:816460
pubmed: 26089604
Trends Mol Med. 2019 Feb;25(2):149-163
pubmed: 30711482
Front Med (Lausanne). 2018 May 15;5:142
pubmed: 29868594
Br Med J. 1961 Nov 4;2(5261):1165-72
pubmed: 14497750
Stem Cells. 2016 Sep;34(9):2429-42
pubmed: 27299362
Clin Immunol. 2010 Oct;137(1):89-101
pubmed: 20674506
Am J Respir Crit Care Med. 2001 Jun;163(7):1540-5
pubmed: 11401870
Nat Genet. 2005 Apr;37(4):357-64
pubmed: 15735647
Cytotherapy. 2018 Mar;20(3):273-278
pubmed: 29434007
Nucl Med Biol. 2011 Oct;38(7):961-7
pubmed: 21810549
Exp Hematol. 2007 Mar;35(3):426-33
pubmed: 17309823
Curr Protoc Immunol. 2013 Oct 01;102:Unit 22F.12.
pubmed: 24510517
Exp Hematol. 2009 Dec;37(12):1445-53
pubmed: 19772890
Proc Natl Acad Sci U S A. 1994 May 24;91(11):4965-9
pubmed: 7910965
J Exp Med. 2017 Aug 7;214(8):2387-2404
pubmed: 28694385
J Cell Biochem. 2012 Sep;113(9):2806-12
pubmed: 22511358
Nat Genet. 2008 Sep;40(9):1103-6
pubmed: 19165924
Sarcoidosis Vasc Diffuse Lung Dis. 2016 Mar 29;33(1):17-28
pubmed: 27055832
Curr Mol Med. 2013 Jun;13(5):856-67
pubmed: 23642066
Oncotarget. 2017 May 2;8(18):30511-30523
pubmed: 28430622
Respiration. 2018;96(2):148-158
pubmed: 29719298
Am J Respir Cell Mol Biol. 2016 Jan;54(1):13-24
pubmed: 26267148
Chest. 2017 May;151(5):971-981
pubmed: 27890713
Lancet. 2004 May 1;363(9419):1439-41
pubmed: 15121408
Immunol Lett. 2015 Dec;168(2):208-14
pubmed: 26051681
Am J Respir Crit Care Med. 1995 Sep;152(3):1061-6
pubmed: 7663784
J Orthop Res. 1991 Sep;9(5):641-50
pubmed: 1870029
Dig Dis Sci. 2017 Apr;62(4):851-860
pubmed: 28168575
Nat Rev Immunol. 2014 Feb;14(2):81-93
pubmed: 24445666
J Transl Med. 2013 Jul 15;11:171
pubmed: 23855653
Sarcoidosis Vasc Diffuse Lung Dis. 2015 Jul 22;32(2):106-14
pubmed: 26278689
Bull Exp Biol Med. 2018 Mar;164(4):576-578
pubmed: 29504107
Respirology. 2014 Oct;19(7):1013-8
pubmed: 25039426
Adv Exp Med Biol. 2016;951:77-98
pubmed: 27837556
Stem Cells Transl Med. 2015 Jun;4(6):615-24
pubmed: 25925837
Thorax. 2011 Feb;66(2):144-50
pubmed: 21139119
Chest. 2018 Jun;153(6):1432-1442
pubmed: 29224832
JAMA. 2011 Jan 26;305(4):391-9
pubmed: 21266686
Eur Respir J. 2003 Mar;21(3):421-8
pubmed: 12661995
Thorax. 2018 Jun;73(6):565-574
pubmed: 29653970
Nat Med. 2009 Jan;15(1):42-9
pubmed: 19098906
J Immunol. 2014 May 15;192(10):4560-4570
pubmed: 24711618
Stem Cell Res Ther. 2018 Feb 26;9(1):45
pubmed: 29482654
Nat Med. 2012 Apr 15;18(5):759-65
pubmed: 22504485
Expert Rev Clin Pharmacol. 2018 Jul;11(7):677-687
pubmed: 29883224
Front Immunol. 2012 Sep 26;3:297
pubmed: 23056000
Blood. 2005 Mar 1;105(5):2214-9
pubmed: 15514012
Stem Cells. 2016 Jul;34(7):1909-21
pubmed: 27015881
J Aerosol Med Pulm Drug Deliv. 2014 Feb;27(1):30-4
pubmed: 23409833

Auteurs

Ian McClain Caldwell (I)

Adult Stem Cell Section, National Institute of Dental and Craniofacial Research (NIDCR), National Institutes of Health (NIH), Bethesda, MD 20892, USA.

Christopher Hogden (C)

Adult Stem Cell Section, National Institute of Dental and Craniofacial Research (NIDCR), National Institutes of Health (NIH), Bethesda, MD 20892, USA.

Krisztian Nemeth (K)

Adult Stem Cell Section, National Institute of Dental and Craniofacial Research (NIDCR), National Institutes of Health (NIH), Bethesda, MD 20892, USA.
Stem Cell Laboratory, Department of Dermatology, Venerology and Dermato-oncology, Semmelweis University, Budapest 1085, Hungary.

Michael Boyajian (M)

Adult Stem Cell Section, National Institute of Dental and Craniofacial Research (NIDCR), National Institutes of Health (NIH), Bethesda, MD 20892, USA.

Miklos Krepuska (M)

Adult Stem Cell Section, National Institute of Dental and Craniofacial Research (NIDCR), National Institutes of Health (NIH), Bethesda, MD 20892, USA.

Gergely Szombath (G)

Stem Cell Laboratory, Department of Dermatology, Venerology and Dermato-oncology, Semmelweis University, Budapest 1085, Hungary.

Sandra MacDonald (S)

National Heart, Lung, and Blood Institute (NHLBI), NIH, Bethesda, MD 20892, USA.

Mehrnoosh Abshari (M)

Combined Technical Research Core, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892, USA.

Joel Moss (J)

National Heart, Lung, and Blood Institute (NHLBI), NIH, Bethesda, MD 20892, USA.

Lynn Vitale-Cross (L)

Adult Stem Cell Section, National Institute of Dental and Craniofacial Research (NIDCR), National Institutes of Health (NIH), Bethesda, MD 20892, USA.

Joseph R Fontana (JR)

National Heart, Lung, and Blood Institute (NHLBI), NIH, Bethesda, MD 20892, USA.

Eva Mezey (E)

Adult Stem Cell Section, National Institute of Dental and Craniofacial Research (NIDCR), National Institutes of Health (NIH), Bethesda, MD 20892, USA.

Classifications MeSH