Bizingre Chloé, Arellano-Anaya Zaira, Picard Flavien, Pietri Mathéa, Baudry Anne, Roussel Florence, Bianchi Clara, Alleaume-Butaux Aurélie, Ardila-Osorio Hector, Romao Maryse, Lavieu Grégory, Raposo Graça, Schneider Benoit
INSERM UMR-S 1124, Paris, France.
Université Paris Cité, UMR-S 1124, Paris, France.
J Extracell Vesicles. 2025 Jul;14(7):e70114. doi: 10.1002/jev2.70114.
Small extracellular vesicles (SEVs) are involved in diverse functions in normal and pathological situations, including intercellular communication, immunity, metastasis and neurodegeneration. Cell release of SEVs is assumed to occur passively right after multivesicular bodies of the endocytic pathway fuse with the plasma membrane. We show here that the completion of SEV release depends on membrane-bound ADAM10 and ADAM17 sheddases that promote the detachment of SEVs from the cell surface by catalysing the cleavage of adhesion proteins of the SEV membrane. The intensity of ADAM10/17-mediated release of SEVs depends on a balanced control of 3-phosphoinositide-dependent kinase 1 (PDK1) and ERK1/2 signalling pathways converging on 90-kDa ribosomal S6 kinase-2 (RSK2), which, in turn, fine-tunes ADAM17 bioavailability and ADAM10/17 enzymatic activities at the plasma membrane, according to a mechanism that relies, at least in part, on variation of the rhomboid-like pseudoprotease iRhom2 cell surface level. By identifying a new proteolytic step involved in the basal release of SEVs, our work may help understand how the deregulation of ADAM10/17-mediated discharge of SEVs contributes to several pathological states.
小细胞外囊泡(SEV)在正常和病理情况下参与多种功能,包括细胞间通讯、免疫、转移和神经退行性变。SEV的细胞释放被认为是在内吞途径的多囊泡体与质膜融合后立即被动发生的。我们在此表明,SEV释放的完成取决于膜结合的ADAM10和ADAM17蛋白酶,它们通过催化SEV膜粘附蛋白的裂解来促进SEV从细胞表面脱离。ADAM10/17介导的SEV释放强度取决于对3-磷酸肌醇依赖性激酶1(PDK1)和ERK1/2信号通路的平衡控制,这两条信号通路汇聚于90 kDa核糖体S6激酶2(RSK2),而RSK2又根据一种至少部分依赖于类菱形假蛋白酶iRhom2细胞表面水平变化的机制,对质膜上ADAM17的生物利用度和ADAM10/17的酶活性进行微调。通过确定SEV基础释放中涉及的一个新的蛋白水解步骤,我们的工作可能有助于理解ADAM10/17介导的SEV释放失调如何导致多种病理状态。