C-C Chemokine Receptor 7 Promotes T-Cell Acute Lymphoblastic Leukemia Invasion of the Central Nervous System via β2-Integrins.
Cesar I CardonaAlondra RodriguezVivian C TorresAnahi SanchezAngel TorresAaron E VazquezAmy E WaglerMichael A BrissetteColin A BillCharlotte M VinesPublished in: International journal of molecular sciences (2024)
C-C Chemokine Receptor 7 (CCR7) mediates T-cell acute lymphoblastic leukemia (T-ALL) invasion of the central nervous system (CNS) mediated by chemotactic migration to C-C chemokine ligand 19 (CCL19). To determine if a CCL19 antagonist, CCL19 8-83 , could inhibit CCR7-induced chemotaxis and signaling via CCL19 but not CCL21, we used transwell migration and Ca 2+ mobilization signaling assays. We found that in response to CCL19, human T-ALL cells employ β2 integrins to invade human brain microvascular endothelial cell monolayers. In vivo, using an inducible mouse model of T-ALL, we found that we were able to increase the survival of the mice treated with CCL19 8-83 when compared to non-treated controls. Overall, our results describe a targetable cell surface receptor, CCR7, which can be inhibited to prevent β2-integrin-mediated T-ALL invasion of the CNS and potentially provides a platform for the pharmacological inhibition of T-ALL cell entry into the CNS.
Keyphrases
- liver fibrosis
- liver injury
- acute lymphoblastic leukemia
- drug induced
- endothelial cells
- cell migration
- mouse model
- blood brain barrier
- regulatory t cells
- high glucose
- allogeneic hematopoietic stem cell transplantation
- induced apoptosis
- cell proliferation
- immune response
- signaling pathway
- type diabetes
- cell therapy
- cerebrospinal fluid
- binding protein
- metabolic syndrome
- pi k akt
- stress induced