Human umbilical cord mesenchymal stromal cells attenuate pulmonary fibrosis via regulatory T cell through interaction with macrophage

• DOI: 10.1186/s13287-021-02469-5
• Publication Date: 2021-07-13T13:03:26Z
• Authors: Zan Tang; Junxiao Gao; Jie Wu; Guifang Zeng; Yan Liao; Zhenkun Song; Xiao Liang; Junyuan Hu; Yong Hu; Muyun Liu; Nan Li
• Keywords: 0301 basic medicine; Medicine (General); Human umbilical cord mesenchymal stromal cell; Macrophage; Research; Macrophages; Pulmonary Fibrosis; Mesenchymal Stem Cells; QD415-436; Biochemistry; T-Lymphocytes, Regulatory; Umbilical Cord; 3. Good health; Mice; 03 medical and health sciences; R5-920; Animals; Humans; Single cell RNA sequencing; Regulatory T cell

Abstract Background Pulmonary fibrosis (PF) is a growing clinical problem with limited therapeutic options. Human umbilical cord mesenchymal stromal cell (hucMSC) therapy is being investigated in clinical trials for the treatment of PF patients. However, little is known about the underlying molecular and cellular mechanisms of hucMSC therapy on PF. In this study, the molecular and cellular behavior of hucMSC was investigated in a bleomycin-induced mouse PF model.

Methods The effect of hucMSCs on mouse lung regeneration was determined by detecting Ki67 expression and EdU incorporation in alveolar type 2 (AT2) and lung fibroblast cells. hucMSCs were transfected to express the membrane localized GFP before transplant into the mouse lung. The cellular behavior of hucMSCs in mouse lung was tracked by GFP staining. Single cell RNA sequencing was performed to investigate the effects of hucMSCs on gene expression profiles of macrophages after bleomycin treatment.

Results hucMSCs could alleviate collagen accumulation in lung and decrease the mortality of mouse induced by bleomycin. hucMSC transplantation promoted AT2 cell proliferation and inhibited lung fibroblast cell proliferation. By using single cell RNA sequencing, a subcluster of interferon-sensitive macrophages (IFNSMs) were identified after hucMSC infusion. These IFNSMs elevate the secretion of CXCL9 and CXCL10 following hucMSC infusion and recruit more Treg cells to the injured lung.

Conclusions Our study establishes a link between hucMSCs, macrophage, Treg, and PF. It provides new insights into how hucMSCs interact with macrophage during the repair process of bleomycin-induced PF and play its immunoregulation function.