Three-dimensional cultured human umbilical cord mesenchymal stem cells attenuate pulmonary fibrosis by improving the balance of mitochondrial fusion and fission

Author:

Zhai Huifang1,Jiang Mengqi2,Zhao Yaqin3,Wang Yujie2,Zhang Haitong3,Ji Yunxia3,Song Xiaodong2,Zhang Jinjin2,Lv Changjun3,Li Minge1ORCID

Affiliation:

1. Department of Clinical Nursing, Binzhou Medical University Hospital, Binzhou Medical University , Binzhou 256603 , People’s Republic of China

2. Department of Cellular and Genetic Medicine, Binzhou Medical University , Yantai 264003 , People’s Republic of China

3. Department of Respiratory and Critical Care Medicine, Binzhou Medical University Hospital, Binzhou Medical University , Binzhou 256603 , People’s Republic of China

Abstract

Abstract Pulmonary fibrosis is a kind of fibrotic interstitial pneumonia with poor prognosis. Aging, environmental pollution, and coronavirus disease 2019 are considered as independent risk factors for pulmonary fibrogenesis. Consequently, the morbidity and mortality striking continues to rise in recent years. However, the clinical therapeutic efficacy is very limited and unsatisfactory. So it is necessary to develop a new effective therapeutic approach for pulmonary fibrosis. Human umbilical cord mesenchymal stem cells (hucMSCs) are considered as a promising treatment for various diseases because of their multiple differentiation and immunomodulatory function. The key bottleneck in the clinical application of hucMSCs therapy is the high-quality and large-scale production. This study used FloTrix miniSpin bioreactor, a three-dimensional (3D) cell culture system, for large-scale expansion of hucMSCs in vitro, and proved 3D cultured hucMSCs inhibited the differentiation of fibroblasts into myofibroblasts and myofibroblasts proliferation and migration, leading to slow down the development of pulmonary fibrosis. Further mechanistic studies clarified that hucMSCs reduced the amount of binding between circELP2 and miR-630, resulting in blocking YAP/TAZ translocation from cytoplasm to nucleus. This condition inhibited mitochondrial fusion and promoted mitochondrial fission, and ultimately improved fusion/fission balance and cellular homeostasis. To sum up, this work clarified the anti-fibrosis and mechanism of hucMSCs cultured from the 3D FloTrix miniSpin bioreactor. We hope to provide new ideas and new methods for the clinical transformation and industrialization of hucMSCs therapy.

Funder

National Natural Science Foundation of China

Publisher

Oxford University Press (OUP)

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