| First Author | Ullah I | Year | 2023 |
| Journal | J Cell Sci | Volume | 136 |
| Issue | 14 | PubMed ID | 37357611 |
| Mgi Jnum | J:359939 | Mgi Id | MGI:7565981 |
| Doi | 10.1242/jcs.260809 | Citation | Ullah I, et al. (2023) Src- and Abl-family kinases activate spleen tyrosine kinase to maximize phagocytosis and Leishmania infection. J Cell Sci 136(14) |
| abstractText | Leishmania spp. are obligate intracellular parasites that must be internalized by phagocytic cells to evade immune responses and cause disease. The uptake of both Leishmania promastigotes (insect-stage parasites) and amastigotes (proliferative-stage parasites in humans and mice) by phagocytes is thought to be mainly host cell driven, not parasite driven. Our previous work indicates that host Src- and Abl-family kinases facilitate Leishmania entry into macrophages and pathogenesis in murine cutaneous leishmaniasis. Here, we demonstrate that host spleen tyrosine kinase (SYK) is required for efficient uptake of Leishmania promastigotes and amastigotes. A Src-family kinase-Abl-family kinase-SYK signaling cascade induces Leishmania amastigote internalization. Finally, lesion size and parasite burden during Leishmania infection is significantly decreased in mice lacking SYK in monocytes or by treatment with the SYK inhibitor entospletinib. In summary, SYK is required for maximal Leishmania uptake by macrophages and disease in mice. Our results suggest potential for treating leishmaniasis using host cell-directed agents. |
