1 School of Interdisciplinary Bioscience and Bioengineering, Pohang University of Science and Technology, Pohang, Gyeongbuk, Republic of Korea.
2 Department of Mechanical Engineering, Pohang University of Science and Technology, Pohang, Gyeongbuk, Republic of Korea.
J Dent Res. 2017 Jul;96(8):938-944. doi: 10.1177/0022034517702100. Epub 2017 Apr 14.
Saliva contains biological information as blood and is recognized as a valuable diagnostic medium for their noninvasiveness. Although "-omics" researches have tried to investigate saliva, the origin and significance of its contents are not clear, and its usage is largely confined to oral disease in the diagnostic and prognostic field. In an attempt to broaden the applicability of saliva and to find systemic disease-derived RNA in saliva, we made mouse models that had human melanoma and isolated extracellular vesicles (EVs) from their saliva by an aqueous 2-phase system (ATPS), then identified and evaluated their expression of human melan-A RNA, which is associated with melanoma on skin. With ATPS, EVs were isolated efficiently and stably while taking less time compared to isolation by ultracentrifugation. When ATPS was used to isolate EVs from saliva, the mean ± SD percentage of EVs recovered from initial EVs was 38.22% ± 18.55% by the number of particles, and the mean ± SD percentage of RNA recovered from the initial amount was 60.33% ± 5.34%. RNAs within isolated EVs were analyzed subsequently by reverse transcription quantitative polymerase chain reaction and polymerase chain reaction from saliva and plasma. In melanoma mice, amplification of human melan-A was identified from saliva and plasma, even though a relative amount of normalized melan-A was lower than that of plasma. These results present a possibility that RNAs derived from systemic disease are transferred into saliva from blood in EVs. Also, they suggest that saliva could be exploited in obtaining information about systemic disease, not only about oral disease, by examining RNAs in EVs from saliva instead of blood.
唾液中含有生物信息,如同血液一样,并且因其无创性而被认为是一种有价值的诊断介质。尽管“组学”研究试图探索唾液,但它的来源和意义尚不清楚,其用途在很大程度上局限于口腔疾病的诊断和预后领域。为了扩大唾液的适用性,并在唾液中寻找系统性疾病来源的 RNA,我们构建了携带人类黑色素瘤的小鼠模型,并用双水相系统(ATPS)从其唾液中分离细胞外囊泡(EVs),然后鉴定和评估与皮肤黑色素瘤相关的人黑色素-A RNA 的表达。与超速离心法相比,使用 ATPS 可以更有效地分离 EVs,并且用时更短。当使用 ATPS 从唾液中分离 EVs 时,通过颗粒数计算,初始 EVs 中回收的 EVs 的平均值±SD 百分比为 38.22%±18.55%,初始量中回收的 RNA 的平均值±SD 百分比为 60.33%±5.34%。随后通过逆转录定量聚合酶链反应和聚合酶链反应分析分离出的 EV 内的 RNA。在黑色素瘤小鼠中,即使标准化黑色素-A 的相对量低于血浆,也能从唾液和血浆中鉴定出人类黑色素-A 的扩增。这些结果表明,来自系统性疾病的 RNA 可能通过 EV 从血液转移到唾液中。此外,这些结果还表明,通过检查唾液中 EV 中的 RNA,而不是血液中的 RNA,唾液可以用于获取有关系统性疾病的信息,而不仅仅是口腔疾病的信息。