TY - JOUR
T1 - Proteomic analysis of exosomes from nasopharyngeal carcinoma cell identifies intercellular transfer of angiogenic proteins
AU - Chan, Yuk-Kit
AU - Zhang, Huoming
AU - Liu, Pei
AU - Tsao, Sai-Wah
AU - Lung, Maria Li
AU - Mak, Nai-Ki
AU - Wong, Ricky Ngok-Shun
AU - Yue, Patrick Ying-Kit
N1 - Grant sponsor: AoE NPC; Grant number: AoE/M-06/08, GRF17120814
PY - 2015/10
Y1 - 2015/10
N2 - Exosomes, a group of secreted extracellular nanovesicles containing genetic materials and signaling molecules, play a critical role in intercellular communication. During tumorigenesis, exosomes have been demonstrated to promote tumor angiogenesis and metastasis while their biological functions in nasopharyngeal carcinoma (NPC) are poorly understood. In this study, we focused on the role of NPC-derived exosomes on angiogenesis. Exosomes derived from the NPC C666-1 cells and immortalized nasopharyngeal epithelial cells (NP69 and NP460) were isolated using ultracentrifugation. The molecular profile and biophysical characteristics of exosomes were verified by Western blotting, sucrose density gradient and electron microscopy. We showed that the C666-1 exosomes (10 and 20 μg/ml) could significantly increase the tubulogenesis, migration and invasion of human umbilical vein endothelial cells (HUVECs) in a dose-dependent manner. Subsequently, an iTRAQ-based quantitative proteomics was used to identify the differentially expressed proteins in C666-1 exosomes. Among the 640 identified proteins, 51 and 89 proteins were considered as up- and down-regulated (≥ 1.5-fold variations) in C666-1 exosomes compared to the normal counterparts, respectively. As expected, pro-angiogenic proteins including intercellular adhesion molecule-1 (ICAM-1) and CD44 variant isoform 5 (CD44v5) are among the up-regulated proteins, whereas angio-suppressive protein, thrombospondin-1 (TSP-1) was down-regulated in C666-1 exosomes. Further confocal microscopic study and Western blotting clearly demonstrated that the alteration of ICAM-1 and TSP-1 expressions in recipient HUVECs are due to internalization of exosomes. Taken together, these data strongly indicated the critical roles of identified angiogenic proteins in the involvement of exosomes-induced angiogenesis, which could potentially be developed as therapeutic targets in future. What's new? Many cells secrete exosomes. These nanoscale vesicles contain signaling molecules, mRNA, and miRNA, and play a critical role in intercellular communication. In this study, the authors identified several angiogenic factors in exosomes from nasopharyngeal carcinoma (NPC) cells. Purified NPC exosomes also caused normal endothelial cells to change to an angiogenic phenotype. These findings shed new light on the mechanisms by which NPC tumors may increase their blood supply, and also suggest that these exosomes may offer a promising therapeutic target.
AB - Exosomes, a group of secreted extracellular nanovesicles containing genetic materials and signaling molecules, play a critical role in intercellular communication. During tumorigenesis, exosomes have been demonstrated to promote tumor angiogenesis and metastasis while their biological functions in nasopharyngeal carcinoma (NPC) are poorly understood. In this study, we focused on the role of NPC-derived exosomes on angiogenesis. Exosomes derived from the NPC C666-1 cells and immortalized nasopharyngeal epithelial cells (NP69 and NP460) were isolated using ultracentrifugation. The molecular profile and biophysical characteristics of exosomes were verified by Western blotting, sucrose density gradient and electron microscopy. We showed that the C666-1 exosomes (10 and 20 μg/ml) could significantly increase the tubulogenesis, migration and invasion of human umbilical vein endothelial cells (HUVECs) in a dose-dependent manner. Subsequently, an iTRAQ-based quantitative proteomics was used to identify the differentially expressed proteins in C666-1 exosomes. Among the 640 identified proteins, 51 and 89 proteins were considered as up- and down-regulated (≥ 1.5-fold variations) in C666-1 exosomes compared to the normal counterparts, respectively. As expected, pro-angiogenic proteins including intercellular adhesion molecule-1 (ICAM-1) and CD44 variant isoform 5 (CD44v5) are among the up-regulated proteins, whereas angio-suppressive protein, thrombospondin-1 (TSP-1) was down-regulated in C666-1 exosomes. Further confocal microscopic study and Western blotting clearly demonstrated that the alteration of ICAM-1 and TSP-1 expressions in recipient HUVECs are due to internalization of exosomes. Taken together, these data strongly indicated the critical roles of identified angiogenic proteins in the involvement of exosomes-induced angiogenesis, which could potentially be developed as therapeutic targets in future. What's new? Many cells secrete exosomes. These nanoscale vesicles contain signaling molecules, mRNA, and miRNA, and play a critical role in intercellular communication. In this study, the authors identified several angiogenic factors in exosomes from nasopharyngeal carcinoma (NPC) cells. Purified NPC exosomes also caused normal endothelial cells to change to an angiogenic phenotype. These findings shed new light on the mechanisms by which NPC tumors may increase their blood supply, and also suggest that these exosomes may offer a promising therapeutic target.
KW - Angiogenesis
KW - Exosomes
KW - iTRAQ
KW - Nasopharyngeal carcinoma
KW - Proteomic
UR - http://www.scopus.com/inward/record.url?scp=84938952292&partnerID=8YFLogxK
U2 - 10.1002/ijc.29562
DO - 10.1002/ijc.29562
M3 - Journal article
C2 - 25857718
AN - SCOPUS:84938952292
SN - 0020-7136
VL - 137
SP - 1830
EP - 1841
JO - International Journal of Cancer
JF - International Journal of Cancer
IS - 8
ER -