Department of Pharmacology, Stony Brook University Renaissance School of Medicine, Stony Brook, NY 11794, USA.
Department of Microbiology and Immunology, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.
Viruses. 2020 Oct 1;12(10):1117. doi: 10.3390/v12101117.
Although extracellular vesicle (EV) surface electrostatic properties (measured as zeta potential, ζ-potential) have been reported by many investigators, the biophysical implications of charge and EV origin remains uncertain. Here, we compared the ζ-potential of human blood EVs (BEVs) and semen EVs (SEVs) from 26 donors that were HIV-infected (HIV+, = 13) or HIV uninfected (HIV-, = 13). We found that, compared to BEVs that bear neutral surface charge, SEVs were significantly more negatively charged, even when BEVs and SEVs were from the same individual. Comparison of BEVs and SEVs from HIV- and HIV+ groups revealed subtle HIV-induced alteration in the ζ-potential of EVs, with the effect being more significant in SEVs (∆ζ-potential = -8.82 mV, -value = 0.0062) than BEVs (∆ζ-potential = -1.4 mV, -value = 0.0462). These observations were validated by differences in the isoelectric point (IEP) of EVs, which was in the order of HIV + SEV ≤ HIV-SEV ≪ HIV + BEV ≤ HIV-BEV. Functionally, the rate and efficiency of SEV internalization by the human cervical epithelial cell line, primary peripheral blood lymphocytes, and primary blood-derived monocytes were significantly higher than those of BEVs. Mechanistically, removal of sialic acids from the surface of EVs using neuraminidase treatment significantly decreased SEV's surface charge, concomitant with a substantial reduction in SEV's internalization. The neuraminidase effect was independent of HIV infection and insignificant for BEVs. Finally, these results were corroborated by enrichment of glycoproteins in SEVs versus BEVs. Taken together, these findings uncover fundamental tissue-specific differences in surface electrostatic properties of EVs and highlight the critical role of surface charge in EV/target cell interactions.
尽管许多研究人员已经报道了细胞外囊泡(EV)的表面静电特性(以 ζ-电位测量),但电荷和 EV 起源的生物物理意义仍不确定。在这里,我们比较了来自 26 名供体的人类血液 EV(BEV)和精液 EV(SEV)的 ζ-电位,这些供体中 HIV 感染(HIV+,n=13)或未感染(HIV-,n=13)。我们发现,与表面带中性电荷的 BEV 相比,SEV 带负电荷的程度明显更高,即使 BEV 和 SEV 来自同一个体。HIV-和 HIV+组的 BEV 和 SEV 比较显示,EV 的 ζ-电位有微妙的 HIV 诱导改变,而 SEV 的影响更为显著(∆ζ-电位=-8.82 mV,-值=0.0062),而非 BEV(∆ζ-电位=-1.4 mV,-值=0.0462)。这些观察结果通过 EV 等电点(IEP)的差异得到验证,EV 的 IEP 顺序为 HIV+SEV≤HIV-SEV≪HIV+BEV≤HIV-BEV。在功能上,SEV 被人宫颈上皮细胞系、原代外周血淋巴细胞和原代血源性单核细胞内化的速率和效率明显高于 BEV。从机制上讲,用神经氨酸酶处理去除 EV 表面的唾液酸会显著降低 SEV 的表面电荷,同时大大降低 SEV 的内化。神经氨酸酶的作用与 HIV 感染无关,对 BEV 影响不大。最后,这些结果通过 SEV 相对于 BEV 中糖蛋白的富集得到证实。综上所述,这些发现揭示了 EV 表面静电特性的基本组织特异性差异,并强调了表面电荷在 EV/靶细胞相互作用中的关键作用。