| Literature DB >> 31719045 |
Shigeru Okuhara1, Anahid A Birjandi2, Hadeel Adel Al-Lami2, Tomoko Sagai3, Takanori Amano3, Toshihiko Shiroishi3, Guilherme M Xavier2, Karen J Liu2, Martyn T Cobourne4, Sachiko Iseki5.
Abstract
The tongue is a highly specialised muscular organ with a complex anatomy required for normal function. We have utilised multiple genetic approaches to investigate local temporospatial requirements for sonic hedgehog (SHH) signalling during tongue development. Mice lacking a Shh cis-enhancer, MFCS4 (ShhMFCS4/-), with reduced SHH in dorsal tongue epithelium have perturbed lingual septum tendon formation and disrupted intrinsic muscle patterning, with these defects reproduced following global Shh deletion from E10.5 in pCag-CreERTM; Shhflox/flox embryos. SHH responsiveness was diminished in local cranial neural crest cell (CNCC) populations in both mutants, with SHH targeting these cells through the primary cilium. CNCC-specific deletion of orofaciodigital syndrome 1 (Ofd1), which encodes a ciliary protein, in Wnt1-Cre; Ofdfl/Y mice led to a complete loss of normal myotube arrangement and hypoglossia. In contrast, mesoderm-specific deletion of Ofd1 in Mesp1-Cre; Ofdfl/Y embryos resulted in normal intrinsic muscle arrangement. Collectively, these findings suggest key temporospatial requirements for local SHH signalling in tongue development (specifically, lingual tendon differentiation and intrinsic muscle patterning through signalling to CNCCs) and provide further mechanistic insight into the tongue anomalies seen in patients with disrupted hedgehog signalling.Entities:
Keywords: Neural crest; Sonic hedgehog; Tendon; Tongue
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Year: 2019 PMID: 31719045 DOI: 10.1242/dev.180075
Source DB: PubMed Journal: Development ISSN: 0950-1991 Impact factor: 6.862