Related Experiment Video
Updated: Apr 3, 2026

Impedance-based Real-time Measurement of Cancer Cell Migration and Invasion
Published on: April 2, 2020
CTGF knockdown in Vero cells reduces autophagy and adhesion and promotes short-term suspension adaptation
Runsheng Peng1,2,3, Renhou Jia1,2,3, Rong Huang1,2,3
1Ministry of Education Engineering Research Centre for Key Technology and Industrialisation of Cell-Based Vaccines, Northwest Minzu University, Lanzhou, Gansu, China.
Introduction:
Vero cells are extensively used in viral vaccine production, but their adaptation to serum-free suspension culture is hindered by excessive autophagy and strong anchorage dependence.
Methods:
In this study, we identified Connective Tissue Growth Factor (CTGF/CCN2) as significantly upregulated under starvation-an inducer of autophagy-via RNA-seq screening. A stable CTGF knockdown Vero cell line (knockdown efficiency >50%) was established using lentiviral shRNA.
Results:
Functional characterization demonstrated that CTGF depletion concurrently attenuated autophagic flux (evidenced by reduced LC3-II/I ratio and lysosomal activity) and impaired cell adhesion (with adhesion rates decreased by 50%-60% on extracellular matrix proteins), while maintaining normal cell proliferation.
Discussion:
Our findings reveal a new role for CTGF in regulating the environmental adaptation of Vero cells by coordinating autophagy and adhesion functions. The engineered cell line provides a novel strategy to overcome suspension adaptation bottlenecks, offering significant potential for improving vaccine production scalability.
More Related Videos
07:05TGF-β-mediated Endothelial to Mesenchymal Transition EndMT and the Functional Assessment of EndMT Effectors using CRISPR/Cas9 Gene Editing
Published on: February 26, 2021
11:00Adenovirus-mediated Genetic Removal of Signaling Molecules in Cultured Primary Mouse Embryonic Fibroblasts
Published on: September 9, 2010
Related Concept Videos
Intracellular Signaling Affects Focal Adhesions
Some...
Receptor Downregulation in MVBs
The EGFR can initiate signaling pathways that lead to cell proliferation, migration, and differentiation. Overexpression of EGFR stimulates cells to proliferate. Excessive EGFR...
Cell Motility through Blebbing
Blebbing Through the Matrix
In multicellular...
TGF - β Signaling Pathway