Literature DB >> 20554886

Sulfotransferase Ndst1 is needed for mandibular and TMJ development.

T Yasuda1, C Mundy, T Kinumatsu, Y Shibukawa, T Shibutani, K Grobe, N Minugh-Purvis, M Pacifici, E Koyama.   

Abstract

Heparan sulfate proteoglycans (HS-PGs) regulate several developmental processes, but their possible roles in mandibular and TMJ formation are largely unclear. To uncover such roles, we generated mice lacking Golgi-associated N-sulfotransferase 1 (Ndst1) that catalyzes sulfation of HS-PG glycosaminoglycan chains. Ndst1-null mouse embryos exhibited different degrees of phenotypic penetrance. Severely affected mutants lacked the temporomandibular joint and condyle, but had a mandibular remnant that displayed abnormal tooth germs, substandard angiogenesis, and enhanced apoptosis. In mildly affected mutants, the condylar growth plate was dysfunctional and exhibited thicker superficial and polymorphic cell zones, a much wider distribution of Indian hedgehog signaling activity, and ectopic ossification along its lateral border. Interestingly, mildly affected mutants also exhibited facial asymmetry resembling that seen in individuals with hemifacial microsomia. Our findings indicate that Ndst1-dependent HS sulfation is critical for mandibular and TMJ development and allows HS-PGs to exert their roles via regulation of Ihh signaling topography and action.

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Year:  2010        PMID: 20554886      PMCID: PMC3318048          DOI: 10.1177/0022034510373766

Source DB:  PubMed          Journal:  J Dent Res        ISSN: 0022-0345            Impact factor:   6.116


  33 in total

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Journal:  J Dent Res       Date:  2010-03-03       Impact factor: 6.116

6.  Validity of the Hfm transgenic mouse as a model for hemifacial microsomia.

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Review 10.  Heparan sulfate proteoglycans: structure, protein interactions and cell signaling.

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  15 in total

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Review 3.  Glycosaminoglycan synthesis in the nucleus pulposus: Dysregulation and the pathogenesis of disc degeneration.

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9.  Augmented Indian hedgehog signaling in cranial neural crest cells leads to craniofacial abnormalities and dysplastic temporomandibular joint in mice.

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