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Bone Marrow Mesenchymal Stem Cell-Derived Exosomes Alleviate Diabetic Kidney Disease in Rats by Inhibiting Apoptosis and Inflammation.
Liu, Libo; Zhou, Yuquan; Zhao, Xin; Yang, Xueyao; Wan, Xueqi; An, Ziyu; Zhang, Huan; Tian, Jinfan; Ge, Changjiang; Song, Xiantao.
Afiliação
  • Liu L; Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University, 100029 Beijing, China.
  • Zhou Y; Department of Cardiology, The Second Affiliated Hospital of Shandong First Medical University, 271000 Taian, Shandong, China.
  • Zhao X; Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University, 100029 Beijing, China.
  • Yang X; Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University, 100029 Beijing, China.
  • Wan X; Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University, 100029 Beijing, China.
  • An Z; Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University, 100029 Beijing, China.
  • Zhang H; Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University, 100029 Beijing, China.
  • Tian J; Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University, 100029 Beijing, China.
  • Ge C; Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University, 100029 Beijing, China.
  • Song X; Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University, 100029 Beijing, China.
Front Biosci (Landmark Ed) ; 28(9): 203, 2023 09 14.
Article em En | MEDLINE | ID: mdl-37796685
ABSTRACT
BACKGROUND AND

AIMS:

Previous studies have confirmed the anti-inflammation effect of bone marrow mesenchymal stem cell-derived exosomes (BMSC-Exo). We aimed to investigate the therapeutic effect of BMSC-Exo on diabetic kidney disease (DKD), as well as the underlying mechanisms.

METHODS:

SD rats were induced by streptozotocin combined with a high-fat diet to establish a diabetes disease model. BMSCs-Exo were injected via tail veins at a weekly dose of 100 µg for 12 weeks. Pathological changes in the rat kidneys were evaluated using HE, Masson, and Periodic Acid-Schiff and immunohistochemical staining. TUNEL staining and western blot were used to evaluate the expression levels of apoptosis-related proteins in the rat kidney cells. The TNF-α level was detected by PCR and NF-κB (p65) by western blotting to examine the inflammatory responses in the renal tissue.

RESULTS:

BMSCs-Exo significantly alleviated the renal structural damage and the distribution of apoptotic cells in diabetic rats. Furthermore, BMSCs-Exo increased the expression of pro-apoptosis protein Bax and decreased the expression of apoptosis-executing protein Cleaved Caspase 9 and Cleaved caspase 3. In addition, the transcription level of TNF-α in kidney tissue and NF-κB (p65) expression was also decreased through BMSCs-Exo treatment. Besides, the levels of glucose (GLU), creatinine (Cr), and burea nitrogen (BUN) in diabetic rats were decreased by the BMSC-Exo treatment.

CONCLUSIONS:

BMSCs-Exo may alleviate diabetic kidney damage by inhibiting apoptosis and inflammation.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Experimental / Nefropatias Diabéticas / Exossomos / Células-Tronco Mesenquimais Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Experimental / Nefropatias Diabéticas / Exossomos / Células-Tronco Mesenquimais Idioma: En Ano de publicação: 2023 Tipo de documento: Article