Abstract
Fibrodysplasia ossificans progressiva (FOP) is a rare autosomal dominant congenital disorder characterized by progressive heterotopic ossification in muscle tissues. A constitutively activated mutation of a bone morphogenetic protein (BMP) receptor, ALK2, has been identified in patients with FOP. We report here that four structurally related compounds, lucilactaene, hydroxylucilactaene, NG-391 and NG-393, produced by fungal strain Fusarium sp. B88, inhibit BMP signaling in vitro. Alkaline phosphatase activity, a marker enzyme of osteoblastic differentiation, was decreased in C2C12 myoblasts stably expressing mutant ALK2 by treatment with those compounds with IC50 values of 5.7, 6.8, 6.9 and 6.1μM, respectively. Furthermore, NG-391 and NG-393 inhibited BMP-specific luciferase reporter activity, which is directly regulated by transcription factor Smads, with IC50 values of 1.4 and 2.1μM, respectively. These findings suggest that these fungal metabolites may provide a new direction in the development of FOP therapeutics.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
