Gaspari Giulia, Lange-Consiglio Anna, Cremonesi Fausto, Desantis Salvatore
Laboratory of Reproduction and Regenerative Medicine, Department of Veterinary Medicine and Animal Science (DIVAS), University of Milan, 26900 Lodi, Italy.
Department of Precision and Regenerative Medicine and Ionian Area, University of Bari Aldo Moro, 70010 Valenzano, Italy.
Int J Mol Sci. 2025 Feb 19;26(4):1784. doi: 10.3390/ijms26041784.
Extracellular vesicles (EVs) are important mediators of cell-cell communication thanks to their ability to transfer their bioactive cargo, thus regulating a variety of physiological contexts. EVs derived from amniotic mesenchymal/stromal cells (eAMC-EVs) are internalized by equine endometrial cells (eECs) with positive effects on regenerative medicine treatments. As the cellular uptake of EVs is influenced by the glycan profile of both EVs and target cells, this study is focused on the role of surface glycans in the uptake of eAMC-EVs by recipient eECs. Equine ECs were obtained by enzymatic digestion of uteri from healthy mares. Equine AMC-EVs were isolated from amniotic cell cultures according to a standardized protocol. The glycan pattern was studied using a panel of lectins in combination with fucosidase and neuraminidase treatment. Both eECs and eAMC-EVs expressed N-linked high mannose glycans, as well as fucosylated and sialylated glycans. All these glycans were involved in the uptake of eAMC-EVs by eECs. The internalization of eAMC-EVs was strongly reduced after cleavage of α1,2-linked fucose and α2,3/α2,6-linked sialic acids. These results demonstrate that surface glycans are involved in the internalization of eAMC-EVs by eECs and that fucosylated and sialylated glycans are highly relevant in the transfer of bioactive molecules with effects on regenerative medicine treatments.
细胞外囊泡(EVs)是细胞间通讯的重要介质,因为它们能够传递其生物活性货物,从而调节多种生理环境。源自羊膜间充质/基质细胞的细胞外囊泡(eAMC-EVs)被马子宫内膜细胞(eECs)内化,对再生医学治疗有积极作用。由于细胞外囊泡的细胞摄取受细胞外囊泡和靶细胞聚糖谱的影响,本研究聚焦于表面聚糖在受体eECs摄取eAMC-EVs中的作用。通过酶消化健康母马的子宫获得马子宫内膜细胞。根据标准化方案从羊膜细胞培养物中分离出马羊膜间充质细胞外囊泡。使用一组凝集素结合岩藻糖苷酶和神经氨酸酶处理研究聚糖模式。eECs和eAMC-EVs均表达N-连接的高甘露糖聚糖以及岩藻糖基化和唾液酸化聚糖。所有这些聚糖都参与了eECs对eAMC-EVs的摄取。在切割α1,2-连接的岩藻糖和α2,3/α2,6-连接的唾液酸后,eAMC-EVs的内化作用大大降低。这些结果表明,表面聚糖参与了eECs对eAMC-EVs的内化,并且岩藻糖基化和唾液酸化聚糖在对再生医学治疗有影响的生物活性分子的传递中高度相关。