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Global Translational Medicine                                               Stem cells in aortic aneurysm








































            Figure 1. A schematic overview of cell types in aortic aneurysm and dissection. Various markers representing different cell types are listed in different
            layers of the aortic wall.
            MSC: Mesenchymal stem cell; EC: Endothelial cell; Mast: Mast cells; Neutr: Neutrophils; VSMC: Vascular smooth muscle cell; Macro: Macrophages;
            Mono: Monocytes; DC: Dendritic cells; FibroL: Fibroblasts.

            in the aneurysm lumen, while inhibiting the expression of   promote tissue repair by inducing a macrophage phenotype
            MMP-2 and MMP-9 in aneurysm tissue in vivo .       shift from M1 to M2, which may ultimately prevent the
                                                 [57]
                                                                        [60]
              So far, the effect of EPCs in AA has not been clearly   AA growth . In the process of AAA formation, IL-17
                                                                              +
            concluded, but it can predict the occurrence, development   produced by CD4  T cells can promote inflammation,
                                                                                         [61]
            and rupture of aneurysm at early stage, as well as the   and MSCs can inhibit its effect . In addition to direct
            postoperative outcome.                             regulation, MSCs can also indirectly suppress aortic
                                                               inflammation by modulating microRNAs to attenuate
            3.2. Bone marrow-derived mesenchymal stem cells    AA formation . For example, miR-194 can inhibit
                                                                           [62]
            Bone   marrow-derived  mesenchymal  stem   cells   the expression of BCL2 interacting protein 3 (BNIP3)
                                                                                                           [63]
            (BM-MSCs) are a class of adult stem cells with self-renewal   through KDM3A, inhibiting the progression of AAA .
            and multi-directional differentiation potential, which have   MSC-derived extracellular vesicles also contribute to the
                                                                                                     [64]
            a wide range of roles in AA. Positive markers are found   inhibition of AAA by regulating microRNA-147 . For the
            to be CD73, CD105, CD90, CD29, and STRO2 . Many    hydrolysis of elastin, adult BM-MSC-derived VSMCs can
                                                   [58]
            studies have shown that mesenchymal stem cells (MSCs)   synthesize and assemble elastin to repair and regenerate
                                                                                  [65]
            have an effective therapeutic effect on AA, and the specific   the elastic matrix of AA .
            molecular mechanisms have been widely studied.       Accordingly, MSCs have a good prospect in the
              It is known that the pathogenesis of AA is closely   treatment of AA, but many specific mechanisms are not
            related to vascular inflammation, and MSCs can reduce   fully understood.
            aortic inflammation to treat AA. The inhibitory effect of   3.3. Adipose-derived mesenchymal stem cells
            MSCs on dendritic cells, macrophages and T cells has   (ADSCs)
            long been demonstrated , and the specific mechanism of
                               [59]
            inhibition of inflammation in AA formation has recently   Adipose-derived mesenchymal stem cells (ADSCs) were
            been elucidated. MSCs also reduce inflammation and   also found to play an indispensable role in TAA and AAA.


            Volume 2 Issue 1 (2023)                         4                      https://doi.org/10.36922/gtm.v2i1.241
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