Karvinen Sira, Sievänen Tero, Karppinen Jari E, Hautasaari Pekka, Bart Geneviève, Samoylenko Anatoliy, Vainio Seppo J, Ahtiainen Juha P, Laakkonen Eija K, Kujala Urho M
Gerontology Research Center and Faculty of Sport and Health Sciences, University of Jyväskylä, Jyväskylä, Finland.
Faculty of Sport and Health Sciences, University of Jyväskylä, Jyväskylä, Finland.
Front Physiol. 2020 Jul 15;11:676. doi: 10.3389/fphys.2020.00676. eCollection 2020.
To date, microRNAs (miRs) carried in extracellular vesicles (EVs) in response to exercise have been studied in blood but not in non-invasively collectable body fluids. In the present study, we examined whether six exercise-responsive miRs, miRs-21, -26, -126, -146, -221, and -222, respond to acute endurance exercise stimuli of different intensities in sweat.
We investigated the response of miRs isolated from sweat and serum EVs to three endurance exercise protocols: (1) maximal aerobic capacity (VO ), (2) anaerobic threshold (AnaT), and (3) aerobic threshold (AerT) tests. Sauna bathing was used as a control test to induce sweating through increased body temperature in the absence of exercise. All protocols were performed by the same subjects ( = 8, three males and five females). The occurrence of different miR carriers in sweat and serum was investigated via EV markers (CD9, CD63, and TSG101), an miR-carrier protein (AGO2), and an HDL-particle marker (APOA1) with Western blot. Correlations between miRs in sweat and serum (post-sample) were examined.
Of the studied miR carrier markers, sweat EV fractions expressed CD63 and, very weakly, APOA1, while the serum EV fraction expressed all the studied markers. In sweat EVs, miR-21 level increased after AerT and miR-26 after all the endurance exercise tests compared with the Sauna ( < 0.050). miR-146 after AnaT correlated to sweat and serum EV samples ( = 0.881, = 0.004).
Our preliminary study is the first to show that, in addition to serum, sweat EVs carry miRs. Interestingly, we observed that miRs-21 and -26 in sweat EVs respond to endurance exercise of different intensities. Our data further confirmed that miR responses to endurance exercise in sweat and serum were triggered by exercise and not by increased body temperature. Our results highlight that sweat possesses a unique miR carrier content that should be taken into account when planning analyses from sweat as a substitute for serum.
迄今为止,人们已对血液中响应运动的细胞外囊泡(EV)所携带的微小RNA(miR)进行了研究,但尚未对非侵入性采集的体液进行研究。在本研究中,我们检测了六种运动反应性miR,即miR-21、-26、-126、-146、-221和-222,是否对汗液中不同强度的急性耐力运动刺激产生反应。
我们研究了从汗液和血清EV中分离出的miR对三种耐力运动方案的反应:(1)最大有氧能力(VO )、(2)无氧阈(AnaT)和(3)有氧阈(AerT)测试。使用桑拿浴作为对照测试,在不运动的情况下通过升高体温来诱导出汗。所有方案均由相同的受试者(n = 8,三名男性和五名女性)执行。通过EV标志物(CD9、CD63和TSG101)、miR携带蛋白(AGO2)和高密度脂蛋白颗粒标志物(APOA1)的蛋白质印迹法,研究汗液和血清中不同miR载体的存在情况。检测汗液和血清(采样后)中miR之间的相关性。
在所研究的miR载体标志物中,汗液EV组分表达CD63,APOA1表达非常微弱,而血清EV组分表达所有研究的标志物。在汗液EV中,与桑拿浴相比,AerT后miR-21水平升高,所有耐力运动测试后miR-26水平升高(P < 0.050)。AnaT后的miR-146与汗液和血清EV样本相关(r = 0.881,P = 0.004)。
我们的初步研究首次表明,除血清外,汗液EV也携带miR。有趣的是,我们观察到汗液EV中的miR-21和-26对不同强度的耐力运动有反应。我们的数据进一步证实,汗液和血清中miR对耐力运动的反应是由运动触发的,而不是由体温升高触发的。我们的结果突出表明,汗液具有独特的miR载体成分,在将汗液作为血清替代品进行分析规划时应予以考虑。