4.3 Article

Sertoli Cells Possess Immunomodulatory Properties and the Ability of Mitochondrial Transfer Similar to Mesenchymal Stromal Cells

期刊

STEM CELL REVIEWS AND REPORTS
卷 17, 期 5, 页码 1905-1916

出版社

SPRINGER
DOI: 10.1007/s12015-021-10197-9

关键词

Mesenchymal stem cells; Sertoli cells; Immunomodulation; Mitochondrial transfer

资金

  1. Grant Agency of Charles University [970120]
  2. Grant Agency of the Czech Republic [19-02290S]
  3. Ministry of Health of the Czech Republic [NU21-08-00488]
  4. Charles University programs [4EU +/20/F4/29, SVV 260435, 20604315 PROGRES Q43]

向作者/读者索取更多资源

Sertoli cells (SCs) have been shown to undergo osteogenic, chondrogenic, and adipogenic differentiation successfully, with anti-inflammatory and protective effects. Compared to MSCs, SCs more effectively induce M2 macrophage polarization and regulate inflammatory polarization. Additionally, SCs have demonstrated the ability to transfer mitochondria to immune cells.
It is becoming increasingly evident that selecting an optimal source of mesenchymal stromal cells (MSCs) is crucial for the successful outcome of MSC-based therapies. During the search for cells with potent regenerative properties, Sertoli cells (SCs) have been proven to modulate immune response in both in vitro and in vivo models. Based on morphological properties and expression of surface markers, it has been suggested that SCs could be a kind of MSCs, however, this hypothesis has not been fully confirmed. Therefore, we compared several parameters of MSCs and SCs, with the aim to evaluate the therapeutic potential of SCs in regenerative medicine. We showed that SCs successfully underwent osteogenic, chondrogenic and adipogenic differentiation and determined the expression profile of canonical MSC markers on the SC surface. Besides, SCs rescued T helper (Th) cells from undergoing apoptosis, promoted the anti-inflammatory phenotype of these cells, but did not regulate Th cell proliferation. MSCs impaired the Th17-mediated response; on the other hand, SCs suppressed the inflammatory polarisation in general. SCs induced M2 macrophage polarisation more effectively than MSCs. For the first time, we demonstrated here the ability of SCs to transfer mitochondria to immune cells. Our results indicate that SCs are a type of MSCs and modulate the reactivity of the immune system. Therefore, we suggest that SCs are promising candidates for application in regenerative medicine due to their anti-inflammatory and protective effects, especially in the therapies for diseases associated with testicular tissue inflammation.

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