Ksp37 is a rapidly mobilized NK cell secretory protein that engages FGF2
Charlotte KJC Hermans, Kishan K Chudasama, Axel Berg-Larsen, Ellen M. HaugsteniD, Merete Thune WiigeriD, Alonso Sanchez, Silje Zandstra KrokeideiD, Agnieszka Graczyk-Bartnik, Marta Klopotowska, Malgorzata Firczuk, Jørgen Wesche, Karl-Johan MalmbergiD, Aline PfefferleiD
Abstract
A key feature of natural killer (NK) cells is their preloaded arsenal of effector molecules, allowing them to rapidly respond upon activation. In this study, we characterized a previously unexplored secretory protein, termed killer-specific secretory protein of 37 kDa (Ksp37), which is highly abundant in differentiated CD56dim NK cells. Ksp37 is rapidly secreted in a dose-dependent and JAK-1 dependent manner upon low levels of cytokine stimulation, making it a sensitive readout for NK cell activation. Following secretion, intracellular levels were rapidly replenished, preserving responsiveness to subsequent cytokine stimulation. We found that Ksp37 is stored in polarized intracellular compartments distinct from those containing canonical cytotoxic effector molecules, including granzyme B and perforin, which require stronger stimulation for release. Lastly, we identified Ksp37 as a novel binding partner of fibroblast growth factor 2 (FGF2). This opens new avenues of exploration for the role of NK cells in remodeling their extracellular environment by modulating the FGF2-FGFR1 axis, which plays a key role in tumor growth, angiogenesis and tissue repair.
02 /Specification & Classification
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