Nestin+ Mesenchymal Precursors Generate Distinct Spleen Stromal Cell Subsets and Have Immunomodulatory Function

Mesenchymal stromal cells (MSCs) are known to be widespread in many tissues and possess a broad spectrum of immunoregulatory properties. They have been used in the treatment of a variety of inflammatory diseases; however, the therapeutic effects are still inconsistent owing to their heterogeneity. Spleen stromal cells have evolved to regulate the immune response at many levels as they are bathed in a complex inflammatory milieu during infection. Therefore, it is unknown whether they have stronger immunomodulatory effects than their counterparts derived from other tissues. Here, using a transgenic mouse model expressing GFP driven by the Nestin (Nes) promoter, Nes-GFP(+) cells from bone marrow and spleen were collected. Artificial lymphoid reconstruction in vivo was performed. Cell phenotype, inhibition of T cell inflammatory cytokines, and in vivo therapeutic effects were assessed. We observed Nes-GFP(+) cells colocalized with splenic stromal cells and further demonstrated that these Nes-GFP(+) cells had the ability to establish ectopic lymphoid-like structures in vivo. Moreover, we showed that the Nes-GFP(+) cells possessed the characteristics of MSCs. Spleen-derived Nes-GFP(+) cells exhibited greater immunomodulatory ability in vitro and more remarkable therapeutic efficacy in inflammatory diseases, especially inflammatory bowel disease (IBD) than bone marrow-derived Nes-GFP(+) cells. Overall, our data showed that Nes-GFP(+) cells contributed to subsets of spleen stromal populations and possessed the biological characteristics of MSCs with a stronger immunoregulatory function and therapeutic potential than bone marrow-derived Nes-GFP(+) cells.

Automated summary

This study found that Nes-GFP(+) cells derived from the spleen have stronger immunomodulatory ability and therapeutic potential compared to those derived from bone marrow. These spleen-derived cells also demonstrated the ability to establish ectopic lymphoid-like structures.