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Published on: March 7, 2022
Human 15-lipoxygenase-1 is a regulator of dendritic-cell spreading and podosome formation
Hongya Han1,2, Xiuming Liang2, Monica Ekberg2
1Department of Medicine, Center for Hematology and Regenerative Medicine, Karolinska Institutet, Karolinska University Hospital Huddinge, Stockholm, Sweden; ya.han@ki.se.
Abstract:
Dendritic cells (DCs) involved in proinflammatory immune responses derive mainly from peripheral monocytes, and the cells subsequently mature and migrate into the inflammatory micromilieu. Here we report that suppressing of 15-lipoxygenase-1 led to a substantial reduction in DC spreading and podosome formation in vitro. The surface expression of CD83 was significantly lower in both sh-15-lipoxygenase-1 (15-LOX-1)-transduced cells and DCs cultivated in the presence of a novel specific 15-LOX-1 inhibitor. The T-cell response against tetanus-pulsed DCs was only affected to a minor extent on inhibition of 15-LOX-1. In contrast, endocytosis and migration ability of DCs were significantly suppressed on 15-LOX-1 inhibition. The expression of 15-LOX-1 in DCs was also demonstrated in affected human skin in atopic and contact dermatitis, showing that the enzyme is indeed expressed in inflammatory diseases in vivo. This study demonstrated that inhibiting 15-LOX-1 led to an impaired podosome formation in DCs, and consequently suppressed antigen uptake and migration capacity. These results indicated that 15-LOX-1 is a potential target for inhibiting the trafficking of DCs to lymphoid organs and inflamed tissues and decreasing the inflammatory response attenuating symptoms of certain immunologic and inflammatory disorders such as dermatitis.-Han, H., Liang, X., Ekberg, M., Kritikou, J. S., Brunnström, Å., Pelcman, B., Matl, M., Miao, X., Andersson, M., Yuan, X., Schain, F., Parvin, S., Melin, E., Sjöberg, J., Xu, D., Westerberg, L. S., Björkholm, M., Claesson, H.-E. Human 15-lipoxygenase-1 is a regulator of dendritic-cell spreading and podosome formation.
Insights
Inhibiting 15-lipoxygenase-1 (15-LOX-1) reduces dendritic cell spreading and migration, impacting inflammatory responses. This enzyme is a potential therapeutic target for immune and inflammatory disorders like dermatitis.
Area of Science:
- Immunology
- Cell Biology
- Biochemistry
Background:
- Dendritic cells (DCs) are crucial for initiating proinflammatory immune responses.
- DCs mature and migrate to inflammatory sites, originating from peripheral monocytes.
- Understanding DC regulation is key to managing inflammatory diseases.
Purpose of the Study:
- To investigate the role of 15-lipoxygenase-1 (15-LOX-1) in dendritic cell function.
- To determine the impact of 15-LOX-1 inhibition on DC morphology, migration, and immune response.
- To explore 15-LOX-1 as a potential therapeutic target in inflammatory skin conditions.
Main Methods:
- Utilized shRNA to suppress 15-LOX-1 expression in DCs.
- Employed a specific 15-LOX-1 inhibitor to block enzyme activity.
- Assessed DC spreading, podosome formation, CD83 expression, T-cell response, endocytosis, and migration.
- Examined 15-LOX-1 expression in human skin samples from dermatitis patients.
Main Results:
- 15-LOX-1 suppression significantly reduced DC spreading and podosome formation in vitro.
- Inhibition of 15-LOX-1 led to lower surface CD83 expression on DCs.
- DC endocytosis and migration capabilities were significantly impaired upon 15-LOX-1 inhibition.
- 15-LOX-1 was expressed in human skin affected by atopic and contact dermatitis.
Conclusions:
- 15-LOX-1 plays a critical role in regulating dendritic cell spreading and podosome formation.
- Inhibiting 15-LOX-1 impairs DC antigen uptake and migration, suggesting a role in immune cell trafficking.
- 15-LOX-1 inhibition offers a potential strategy for attenuating inflammatory responses in disorders like dermatitis.
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