TY - JOUR
T1 - IL-4 induces differentiation of human embryonic stem cells into fibrogenic fibroblast-like cells
AU - Sato, Tadashi
AU - Liu, Xiangde
AU - Basma, Hesham
AU - Togo, Shinsaku
AU - Sugiura, Hisatoshi
AU - Nelson, Amy
AU - Nakanishi, Masanori
AU - Kanaji, Nobuhiro
AU - Wang, Xingqi
AU - Kim, Miok
AU - Li, Yingji
AU - Michalski, Joel
AU - Farid, Maha
AU - Sharp, John G.
AU - Rennard, Stephen I.
N1 - Funding Information:
Supported by National Heart, Lung, and Blood Institute RO1-064088 ; the Pulmonary Section, Department of Internal Medicine, the Chancellor’s office, and the Larson Endowment of the University of Nebraska Medical Center (UNMC; to S.I.R.); the Uehara Memorial Foundation and the Japanese Respiratory Research Foundation and the Pfizer Fellowship (to T.S.). The UNMC Microarray Core receives partial support from National Institutes of Health grant P20 RR016469 from the INBRE Program of the National Center for Research Resources .
PY - 2011/6
Y1 - 2011/6
N2 - Background: Fibroblast heterogeneity is recognized, and fibroblasts from diseased tissues, including those of asthmatic subjects, have functional phenotypes that differ from normal tissue. However, progenitor-progeny relationships and the factors that control fibroblast differentiation are poorly defined. Objective: We sought to determine whether IL-4 could alter the functional phenotype of fibroblasts during their differentiation from stem/progenitor cells. Methods: Using a 3-dimensional collagen gel system, we obtained embryoid bodies derived from human embryonic stem cells and recovered spindle-shaped cells consistent with fibroblasts that had differentiated in the presence or absence of IL-4. Results: IL-4-induced fibroblast-like cells were more active in contraction of collagen gels, migration, and production of fibronectin than control (without IL-4) cells. IL-4-induced cells demonstrated less expression of miR-155, which modulated contraction, migration, and fibronectin production. These differences persisted in culture without further addition of IL-4, suggesting the differentiated phenotype might be a permanent alteration. Conclusion: The current study demonstrates that IL-4 induces differentiation of stem/precursor cells into fibroblast-like cells that demonstrate a more fibrogenic phenotype, which is due to reduced expression of miR-155. These findings provide a novel mechanism for the persistent abnormalities in IL-4-related diseases and a novel target to regulate tissue remodeling by fibroblasts.
AB - Background: Fibroblast heterogeneity is recognized, and fibroblasts from diseased tissues, including those of asthmatic subjects, have functional phenotypes that differ from normal tissue. However, progenitor-progeny relationships and the factors that control fibroblast differentiation are poorly defined. Objective: We sought to determine whether IL-4 could alter the functional phenotype of fibroblasts during their differentiation from stem/progenitor cells. Methods: Using a 3-dimensional collagen gel system, we obtained embryoid bodies derived from human embryonic stem cells and recovered spindle-shaped cells consistent with fibroblasts that had differentiated in the presence or absence of IL-4. Results: IL-4-induced fibroblast-like cells were more active in contraction of collagen gels, migration, and production of fibronectin than control (without IL-4) cells. IL-4-induced cells demonstrated less expression of miR-155, which modulated contraction, migration, and fibronectin production. These differences persisted in culture without further addition of IL-4, suggesting the differentiated phenotype might be a permanent alteration. Conclusion: The current study demonstrates that IL-4 induces differentiation of stem/precursor cells into fibroblast-like cells that demonstrate a more fibrogenic phenotype, which is due to reduced expression of miR-155. These findings provide a novel mechanism for the persistent abnormalities in IL-4-related diseases and a novel target to regulate tissue remodeling by fibroblasts.
KW - Embryonic stem cells, fibroblasts, IL-4, fibrosis, asthma, microRNA
KW - miR-155, chemotaxis, collagen gel contraction, TGF-β
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U2 - 10.1016/j.jaci.2011.01.049
DO - 10.1016/j.jaci.2011.01.049
M3 - Article
C2 - 21388667
AN - SCOPUS:79957877529
SN - 0091-6749
VL - 127
SP - 1595-1603.e9
JO - Journal of Allergy and Clinical Immunology
JF - Journal of Allergy and Clinical Immunology
IS - 6
ER -