Science Bite - 3 min Oral Presentation (Students and ECRs only) Lorne Infection and Immunity 2020

Application of activity-based probes to interrogate the contribution of cathepsin X to dendritic cell function (#62)

Bangyan Xu 1 , Justine D Mintern 1 , Laura E Edgington-Mitchell 1 2 3
  1. Department of Biochemistry and Molecular Biology, The University of Melbourne, Parkville, VIC, Australia
  2. Drug Discovery Biology, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, VIC, Australia
  3. Department of Maxillofacial Surgery, College of Dentistry, New York University, New York, USA

Cathepsin X/Z/P (Cat X) is a lysosomal cysteine protease that exhibits unique monocarboxypeptidase activity. Increased Cat X expression is associated with cancer and inflammation, although its roles in normal physiology are still poorly understood. It is expressed by antigen-presenting cells such as dendritic cells (DCs). DCs undergo functional changes upon agonism of pattern recognition receptors (e.g., Toll-like receptors) by pathogen-associated molecular patterns such as CpG. Mature DCs can secrete cytokines, present antigens to T cells, etc. We hypothesise that Cat X contributes to DC function, but this has not been examined in detail until now.

We used activity-based probes, immunoblotting, and immunofluorescence imaging to measure active and total levels of Cat X in naïve DCs (DC1940) or those stimulated with agonists of TLR-3, 4, 6, and 9 (Poly I:C, LPS, R-848, and CpG, respectively). Lysosomal and secreted Cat X levels were significantly elevated in response to CpG treatment, and to a much lesser extent with the other TLR agonists.

To examine the impact of Cat X on DC function, we generated Cat X-deficient DC1940 cells using CRISPR-Cas9. Expression of surface markers indicating DC maturation was unaffected by cathepsin X deficiency. By contrast, we observed a reduction in the secretion of several chemokines and cytokines (CCL3, CCL5, CD14, IL-12 and TNF-α) upon CpG stimulation in Cat X-deficient cells. Cat X-deficient cells exhibited altered processing of cathepsin L, while the activities of other lysosomal proteases were unaffected. We also found that Cat X-deficient cells had impaired proliferation and adhesion.

Collectively, these data indicate that Cat X is strongly upregulated by TLR-9 agonism in DCs. While it may not be essential for DC maturation, Cat X may regulate cytokine secretion, processing of related endolysosomal proteases, proliferation and adhesion. Future studies will examine other features of DC function, including, phagocytosis and antigen processing/presentation.