Interaction network of extracellular vesicles building universal analysis via eye tears: iNEBULA

Author:

Hu Liang12ORCID,Liu Xiaoling12ORCID,Zheng Qiaolan2,Chen Wuhe2ORCID,Xu Hao12,Li Hengrui12,Luo Jiaxin12ORCID,Yang Rui12,Mao Xulong3,Wang Siyao12ORCID,Chen Tucan12ORCID,Lee Luke P.4567ORCID,Liu Fei12ORCID

Affiliation:

1. National Engineering Research Center of Ophthalmology and Optometry, Eye Hospital, Wenzhou Medical University, Wenzhou 325027, China.

2. National Clinical Research Center for Ocular Diseases, Eye Hospital, Wenzhou Medical University, Wenzhou 325027, China.

3. The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, China.

4. Renal Division and Division of Engineering in Medicine, Department of Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA 02115, USA.

5. Department of Bioengineering, University of California at Berkeley, Berkeley, CA 94720, USA.

6. Department of Electrical Engineering and Computer Science, University of California at Berkeley, Berkeley, CA 94720, USA.

7. Institute of Quantum Biophysics, Department of Biophysics, Sungkyunkwan University, Suwon, Gyeonggi-do 16419, Korea.

Abstract

Discovering the secrets of diseases from tear extracellular vesicles (EVs) is well-recognized and appreciated. However, a precise understanding of the interaction network between EV populations and their biogenesis from our body requires more in-depth and systematic analysis. Here, we report the biological profiles of different-size tear EV subsets from healthy individuals and the origins of EV proteins. We have identified about 1800 proteins and revealed the preferential differences in the biogenesis among distinct subsets. We observe that eye-related proteins that maintain retinal homeostasis and regulate inflammation are preferentially enriched in medium-size EVs (100 to 200 nm) fractions. Using universal analysis in combination with the Human Protein Atlas consensus dataset, we found the genesis of tear EV proteins with 37 tissues and 79 cell types. The proteins related to retinal neuronal cells, glial cells, and blood and immune cells are selectively enriched among EV subsets. Our studies in heterogeneous tear EVs provide building blocks for future transformative precision molecular diagnostics and therapeutics.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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