Exosomes are secreted extracellular vesicles that contain bioactive molecules such as proteins and microRNAs. The exosomes have recently drawn considerable interest as they are implicated in many pathophysiological processes such as neurodegeneration, viral propagation, and tumor invasion. Despite the great interests in the medical fields, the basic cell biological understanding of the exosomes is disproportionally lacking. The exosomes are generated when the limiting membranes of endosomes invaginate toward the lumen to form multivesicular bodies (MVBs). The Endosomal Sorting Complex Responsible for Transport (ESCRT) mediates the biogenesis of the exosomes. However, how the exosomes are delivered to the plasma membrane for their release remains elusive. The exocyst is an octameric protein complex consisting of Sec3, Sec5, Sec6, Sec8, Sec10, Sec15, Exo70, and Exo84. The exocyst is thought to mediate the trafficking of protein and lipid cargos from intracellular compartments to the plasma membrane. Our preliminary data revealed that the exocyst directly interacts with the ESCRT and inhibition of the exocyst in cells block exosome secretion. In this proposal, we will first study the molecular mechanisms by which the biogenesis and release of exosomes is coordinated by different members of the exocyst complex. Second, we will investigate how the secretion of exosomes is regulated during tumor cell invasion; a molecular pathway by which oncogenic Akt promotes exosome secretion through the activation of Rab GTPase will be delineated. Our study will contribute to the understanding of the basic biology of exosomes, and shed light to the mechanisms of tumor cell invasion.

Public Health Relevance

Exosomes play important role in many pathophysiological processes such as cardiovascular development, immune responses, host-pathogen interaction, neuronal degeneration, and tumor invasion. Studying the molecular basis and regulatory mechanisms of exosomal trafficking, and how exosomes promote tumor invasion will help us understand many basic physiological processes and bridge the fields of basic exosome biology and cancer biology.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM085146-12
Application #
9915934
Study Section
Nuclear and Cytoplasmic Structure/Function and Dynamics Study Section (NCSD)
Program Officer
Xu, Jianhua
Project Start
2009-06-01
Project End
2021-04-30
Budget Start
2020-05-01
Budget End
2021-04-30
Support Year
12
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
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Lu, Hezhe; Liu, Shujing; Zhang, Gao et al. (2016) Oncogenic BRAF-Mediated Melanoma Cell Invasion. Cell Rep 15:2012-24
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Yu, Shiyan; Yehia, Ghassan; Wang, Juanfei et al. (2014) Global ablation of the mouse Rab11a gene impairs early embryogenesis and matrix metalloproteinase secretion. J Biol Chem 289:32030-43
Das, Amlan; Gajendra, Sangeetha; Falenta, Katarzyna et al. (2014) RalA promotes a direct exocyst-Par6 interaction to regulate polarity in neuronal development. J Cell Sci 127:686-99
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Lu, Hezhe; Liu, Jianglan; Liu, Shujing et al. (2013) Exo70 isoform switching upon epithelial-mesenchymal transition mediates cancer cell invasion. Dev Cell 27:560-73
Cai, Bishuang; Giridharan, Sai Srinivas Panapakkam; Zhang, Jing et al. (2013) Differential roles of C-terminal Eps15 homology domain proteins as vesiculators and tubulators of recycling endosomes. J Biol Chem 288:30172-80

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