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Global Translational Medicine                                               Stem cells in aortic aneurysm



               https://doi.org/10.1161/circulationaha.111.083451     https://doi.org/10.1161/01.Atv.0000142805.20398.74
            62.  Hawkins RB, Salmon M, Su G, et al., 2021, Mesenchymal   72.  Gong J, Zhou D, Jiang L, et al., 2020, In vitro lineage-specific
               stem cells alter microRNA expression and attenuate thoracic   differentiation of vascular smooth muscle cells in response to
               aortic aneurysm formation. J Surg Res, 268: 221–231.   SMAD3 deficiency: Implications for SMAD3-related thoracic
                                                                  aortic aneurysm. Arterioscler Thromb Vasc Biol, 40: 1651–1663.
               https://doi.org/10.1016/j.jss.2021.06.057
                                                                  https://doi.org/10.1161/atvbaha.120.313033
            63.  Zhang H, Wang Y, Bian X,  et al., 2021, MicroRNA-194
               acts as a suppressor during abdominal aortic aneurysm   73.  Wang G, Jacquet L, Karamariti E, et al., 2015, Origin and
               via inhibition of KDM3A-mediated BNIP3.  Life Sci, 277:   differentiation of vascular smooth muscle cells.  J Physiol,
               119309.                                            593: 3013–3030.
               https://doi.org/10.1016/j.lfs.2021.119309          https://doi.org/10.1113/jp270033
            64.  Spinosa M, Lu G, Su G, et al., 2018, Human mesenchymal   74.  Pan H, Xue C, Auerbach BJ, et al., 2020, Single-cell genomics
               stromal cell-derived extracellular vesicles attenuate aortic   reveals a novel cell state during smooth muscle cell phenotypic
               aneurysm formation and macrophage activation via   switching and potential therapeutic targets for atherosclerosis
               microRNA-147. FASEB J, 32: fj201701138RR.          in mouse and human. Circulation, 142: 2060–2075.
               https://doi.org/10.1096/fj.201701138RR             https://doi.org/10.1161/circulationaha.120.048378
            65.  Swaminathan G, Stoilov I, Broekelmann T,  et al., 2018,   75.  Chen PY, Qin L, Li G,  et al., 2020, Smooth muscle cell
               Phenotype-based  selection  of  bone  marrow  mesenchymal   reprogramming in aortic aneurysms.  Cell Stem Cell, 26:
               stem cell-derived smooth muscle cells for elastic matrix   542–557.e511.
               regenerative repair in abdominal aortic aneurysms. J Tissue      https://doi.org/10.1016/j.stem.2020.02.013
               Eng Regen Med, 12: e60–e70.
                                                               76.  Lu S, Jolly AJ, Strand KA, et al., 2020, Smooth muscle-derived
               https://doi.org/10.1002/term.2349                  progenitor cell myofibroblast differentiation through KLF4
            66.  Mildmay-White A, Khan W, 2017, Cell surface markers on   downregulation promotes arterial remodeling and fibrosis.
               adipose-derived stem cells: A systematic review. Curr Stem   JCI Insight, 5: e139445.
               Cell Res Ther, 12: 484–492.                        https://doi.org/10.1172/jci.insight.139445
               https://doi.org/10.2174/1574888x11666160429122133  77.  Cao J, Yang Z, Xiao R, et al., 2020, Regenerative potential
            67.  Xie J, Jones TJ, Feng D, et al., 2017, Human adipose-derived   of pluripotent nontumorgenetic stem cells: Multilineage
               stem cells suppress elastase-induced murine abdominal   differentiating stress enduring cells (Muse cells). Regen Ther,
               aortic inflammation and aneurysm expansion through   15: 92–96.
               paracrine factors. Cell Transplant, 26: 173–189.      https://doi.org/10.1016/j.reth.2020.04.011
               https://doi.org/10.3727/096368916x692212        78.  Peng GY, Lin Y, Li JJ, et al., 2019, The application of induced
            68.  Hu J, Jiang Y, Wu X,  et al., 2022, Exosomal miR-17-5p   pluripotent stem cells in pathogenesis study and gene
               from adipose-derived mesenchymal stem cells inhibits   therapy for vascular disorders: Current progress and future
               abdominal aortic aneurysm by suppressing TXNIP-NLRP3   challenges. Stem Cells Int, 2019: 9613258.
               inflammasome. Stem Cell Res Ther, 13: 349.         https://doi.org/10.1155/2019/9613258
               https://doi.org/10.1186/s13287-022-03037-1      79.  Granata A, Serrano F, Bernard WG, et al., 2017, An iPSC-
            69.  Huang X, Zhang H, Liang X, et al., 2019, Adipose-derived   derived vascular model of Marfan syndrome identifies
               mesenchymal stem cells isolated from patients with   key mediators of smooth muscle cell death. Nat Genet, 49:
               abdominal aortic aneurysm exhibit senescence phenomena.   97–109.
               Oxid Med Cell Longev, 2019: 1305049.               https://doi.org/10.1038/ng.3723
               https://doi.org/10.1155/2019/1305049            80.  Wang Y, Yin P, Bian GL, et al., 2017, The combination of
            70.  Zou S, Ren P, Zhang L,  et al., 2020, Activation of bone   stem cells and tissue engineering: An advanced strategy for
               marrow-derived cells and resident aortic cells during aortic   blood vessels regeneration and vascular disease treatment.
               injury. J Surg Res, 245: 1–12.                     Stem Cell Res Ther, 8: 194.
                                                                  https://doi.org/10.1186/s13287-017-0642-y
               https://doi.org/10.1016/j.jss.2019.07.013
            71.  Sho E, Sho M, Nanjo H,  et al., 2004, Hemodynamic   81.  Rurali E, Perrucci GL, Pilato CA, et al., 2018, Precise therapy
               regulation of CD34+ cell localization and differentiation in   for thoracic aortic aneurysm in Marfan syndrome: A puzzle
               experimental aneurysms. Arterioscler Thromb Vasc Biol, 24:   nearing its solution. Prog Cardiovasc Dis, 61: 328–335.
               1916–1921.                                         https://doi.org/10.1016/j.pcad.2018.07.020


            Volume 2 Issue 1 (2023)                         16                     https://doi.org/10.36922/gtm.v2i1.241
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