Caveolin‐1‐driven membrane remodelling regulates hnRNPK‐mediated exosomal microRNA sorting in cancer
| Autor: | Renee S. Richards, Shivangi Wani, Nicole Cloonan, Vandhana Bharti, Amanda Lewis, Carlos Salomon, Archa H. Fox, Aine Farrell, Jayde E. Ruelcke, Charles S. Bond, Robert G. Parton, David A. Margolin, Michelle M. Hill, Harley Robinson, Li Li, Alexandre S. Cristino, Andrew Lai, Robert A. Gardiner |
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| Jazyk: | angličtina |
| Rok vydání: | 2021 |
| Předmět: |
Male
0301 basic medicine Medicine (General) hnRNPK Caveolin 1 Medicine (miscellaneous) Exosomes Metastasis Heterogeneous-Nuclear Ribonucleoprotein K 03 medical and health sciences 0302 clinical medicine R5-920 RNA‐binding protein Caveolae microRNA medicine Humans cancer RNA Neoplasm cargo Research Articles RNA sequence motif miRNA epigenetics Chemistry Cell Membrane membrane raft Prostatic Neoplasms Cancer Membrane raft Extracellular vesicle medicine.disease Microvesicles Cell biology lipid raft MicroRNAs HEK293 Cells 030104 developmental biology 030220 oncology & carcinogenesis Molecular Medicine extracellular vesicle Colorectal Neoplasms Research Article |
| Zdroj: | Clinical and Translational Medicine Clinical and Translational Medicine, Vol 11, Iss 4, Pp n/a-n/a (2021) |
| ISSN: | 2001-1326 |
| Popis: | Background Caveolae proteins play diverse roles in cancer development and progression. In prostate cancer, non‐caveolar caveolin‐1 (CAV1) promotes metastasis, while CAVIN1 attenuates CAV1‐induced metastasis. Here, we unveil a novel mechanism linking CAV1 to selective loading of exosomes with metastasis‐promoting microRNAs. Results We identify hnRNPK as a CAV1‐regulated microRNA binding protein. In the absence of CAVIN1, non‐caveolar CAV1 drives localisation of hnRPNK to multi‐vesicular bodies (MVBs), recruiting AsUGnA motif‐containing miRNAs and causing their release within exosomes. This process is dependent on the lipid environment of membranes as shown by cholesterol depletion using methyl‐β‐cyclodextrin or by treatment with n‐3 polyunsaturated fatty acids. Consistent with a role in bone metastasis, knockdown of hnRNPK in prostate cancer PC3 cells abolished the ability of PC3 extracellular vesicles (EV) to induce osteoclastogenesis, and biofluid EV hnRNPK is elevated in metastatic prostate and colorectal cancer. Conclusions Taken together, these results support a novel pan‐cancer mechanism for CAV1‐driven exosomal release of hnRNPK and associated miRNA in metastasis, which is modulated by the membrane lipid environment. Highlights 1. Non‐caveolar caveolin‐1 drives non‐canonical localization of hnRNPK to multivesicular bodies (MVB) via membrane raft‐dependent mechanism. 2. MVB localized hnRNPK mediates EV loading of AsUGnA motif‐containing miRNA, which is required for EV‐induced in vitro osteoclastogenesiss. 3. Elevated EV hnRNPK in biofluids from metastatic cancer patients suggest a role as a biomarker. |
| Databáze: | OpenAIRE |
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