Proteomic analysis of serum exosomes derived from Crouzon syndrome patients carrying a mutant FGFR2C342Y
10.3760/cma.j.issn.1009-4598.2018.04.014
- VernacularTitle: Crouzon综合征中FGFR2C342Y基因突变的血清exosome蛋白组学变化
- Author:
Min GE
1
;
Yingzhi WU
;
Ronghu KE
;
Tianyi CAI
;
Junyi YANG
;
Xiongzheng MU
Author Information
1. Huashan Hospital Fudan University, Shanghai 200040, China
- Publication Type:Journal Article
- Keywords:
Crouzon;
Genes;
Exosome;
Proteomic;
Fibronectin1
- From:
Chinese Journal of Plastic Surgery
2018;34(4):299-304
- CountryChina
- Language:Chinese
-
Abstract:
Objective:Reveal the global expression profile of serum exosomal proteins of Crouzon syndrome patients.
Methods:We isolated microvesicles from serum of Crouzon children with a C342Y mutation in FGFR2 by ultracentrifugation, which were further characterized by electron microscopy and immunoblotting. The protein profiling in normal subjects and Crouzon patients was systematically compared by iTRAQ proteomic analysis.
Results:The result demonstrated that microvesicles were between 30—100 nm in diameter, round shape with cup-like concavity and expressed exosomal marker tumor susceptibility gene (TSG) 101 and flotillin (Flot) 1. We identified a total number of 62 proteins, among which 22 proteins overlap with ExoCarta database and were different between the Crouzon patient and the normal subject. The Ingenuity Pathway Analysis showed that the functions of these proteins are mostly involved in Developmental Disorder, Hereditary Disorder, Skeletal and Muscular Disorders, which are all related to the clinical manifestations of Crouzon syndrome. In addition, the proteins were focused on the network of "Organismal Injury and Abnormalities, Hematological System Development and Function, Cell-To-Cell Signaling and Interaction" . The central protein FN1 was presented as the key protein in the network.
Conclusions:Our data demonstrated that serum exosomes harbor informative proteins and FN1 was selected as a potential candidate for its role in promoting osteoblast adhesion, proliferation and mineralization.
