Abstract
ABSTRACTThe bioactivity of Sonic hedgehog (Shh) depends on specific lipid modifications; a palmitate at its N-terminus and a cholesterol at its C-terminus. This dual-lipid modification makes Shh molecules lipophilic, which prevents them from diffusing freely in extracellular space. Multiple lines of evidence indicate that Shh proteins are carried by various forms of extracellular vesicles (EVs). It also has been shown, for instance, that in some tissues Shh proteins are transported to neighboring cells directly via filopodia. We have previously reported that Shh proteins are expressed in hippocampal neurons. In this study we show that, in the hippocampus and cerebellum of postnatal day (P)2 rats, Shh is mostly found near or on the membrane surface of small neurites or filopodia. We also examined cultured hippocampal neurons where we observed noticeable and widespread Shh-immunolabeled vesicles located outside neurons. Through immunoelectron microscopy and biochemical analysis, we find Shh-containing EVs with a wide range of sizes. Unlike robust Shh activity in EVs isolated from cells overexpressing an N-terminal Shh fragment construct, we did not detect measurable Shh activity in EVs purified from the medium of cultured hippocampal neurons. These results suggest the complexity of the transcellular Shh signaling mechanisms in neurons.
Highlights
Sonic hedgehog (Shh) signaling pathway plays critical roles in embryonic development as well as in adult tissue homeostasis (Briscoe and Thérond, 2013; Ferent and Traiffort, 2015)
Immunoblot analysis of HEK293 cells expressing the fulllength Shh or N-terminal fragment of Shh again confirmed the specificity of the antibody (Fig. 1A)
Because multivesicular bodies (MVB) are believed to be a cellular source of exosomes, we focused on identifying exosomes positively labeled with Shh
Summary
Sonic hedgehog (Shh) signaling pathway plays critical roles in embryonic development as well as in adult tissue homeostasis (Briscoe and Thérond, 2013; Ferent and Traiffort, 2015). The 19-kDa N-terminal fragment of Shh undergoes a unique type of modification – with a palmitate added to its N-terminus (Pepinsky et al, 1998) and a cholesterol to its C-terminus (Porter et al, 1996). This dual lipid-modified N-terminal fragment is the signaling molecule that activates the Shh signaling pathway in Shhresponding cells (Chamoun et al, 2001; Lee and Treisman, 2001). It has been reported that EVs with different compositions harbor Shh (Vyas et al, 2014)
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