Structural reconstruction of mouse acute aortic dissection by intravenously administered human Muse cells without immunosuppression.

Autor: Takahashi M; Division of Cardiovascular Surgery and Tohoku University Graduate School of Medicine1-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi, Japan. makoto.t@med.tohoku.ac.jp.; Department of Stem Cell Biology and Histology, Tohoku University Graduate School of Medicine, Sendai, Japan. makoto.t@med.tohoku.ac.jp., Kushida Y; Department of Stem Cell Biology and Histology, Tohoku University Graduate School of Medicine, Sendai, Japan., Kuroda Y; Department of Stem Cell Biology and Histology, Tohoku University Graduate School of Medicine, Sendai, Japan., Wakao S; Department of Stem Cell Biology and Histology, Tohoku University Graduate School of Medicine, Sendai, Japan., Horibata Y; Department of Biochemistry, Dokkyo Medical University School of Medicine, Mibu, Tochigi, Japan., Sugimoto H; Department of Biochemistry, Dokkyo Medical University School of Medicine, Mibu, Tochigi, Japan., Dezawa M; Department of Stem Cell Biology and Histology, Tohoku University Graduate School of Medicine, Sendai, Japan. mdezawa@med.tohoku.ac.jp., Saiki Y; Division of Cardiovascular Surgery and Tohoku University Graduate School of Medicine1-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi, Japan. yoshisaiki@med.tohoku.ac.jp.
Jazyk: angličtina
Zdroj: Communications medicine [Commun Med (Lond)] 2024 Sep 09; Vol. 4 (1), pp. 174. Date of Electronic Publication: 2024 Sep 09.
DOI: 10.1038/s43856-024-00597-6
Abstrakt: Background: Stanford type B-acute aortic dissection (type B-AAD) is often life-threatening without invasive surgery. Multilineage-differentiating stress enduring cell (Muse cells), which comprise several percent of mesenchymal stem cells (MSCs), are endogenous pluripotent-like stem cells that selectively home to damaged tissue and replace damaged/apoptotic cells by in-vivo differentiation.
Methods: Mortality, aortic diameter expansion, cell localization, cell differentiation, and inflammation of the dissected aorta were evaluated in type B-AAD model mice intravenously injected with human-Muse cells, -elastin-knockdown (KD)-Muse cells, -human leukocyte antigen-G (HLA-G)-KD-Muse cells, or MSCs, all without immunosuppressant.
Results: Here, we show the Muse (50,000 cells) group has a lower incidence of aortic rupture and mortality of AAD compared with the MSC-50K (50,000 human-MSCs) and vehicle groups. Spectrum computed tomography in-vivo dynamics and 3-dimensional histologic analyses demonstrate that Muse cells more effectively home to the AAD tissue and survive for 8 weeks in the Muse group than in the MSC-750K (750,000 human-MSCs containing 50,000 Muse cells) group. Homing of Muse cells is impeded in the HLA-G-KD-Muse (50,000 cells) group. Differentiation of homed Muse cells into CD31(+) and alpha-smooth muscle actin (+) cells, production and reorganization of elastic fibers in the AAD tissue, and suppression of diameter expansion are greater in the Muse group than in the MSC-750K and elastin-KD-Muse (50,000 cells) groups.
Conclusions: Intravenously administered Muse cells reconstruct the dissected aorta and improve mortality and diameter enlargement rates. Moreover, small doses of purified Muse cells are more effective than large doses of MSCs. HLA-G is suggested to contribute to the successful survival and homing of Muse cells.
(© 2024. The Author(s).)
Databáze: MEDLINE
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