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Grem2基因敲除小鼠的门齿畸形

Malformation of incisor teeth in Grem2⁻/⁻ mice.

作者信息

Vogel P, Liu J, Platt K A, Read R W, Thiel M, Vance R B, Brommage R

机构信息

Department of Pathology, Lexicon Pharmaceuticals Inc, The Woodlands, TX, USA

Department of Metabolism, Lexicon Pharmaceuticals Inc, The Woodlands, TX, USA.

出版信息

Vet Pathol. 2015 Jan;52(1):224-9. doi: 10.1177/0300985814528218. Epub 2014 Mar 31.

Abstract

GREMLIN 2 (GREM2)--formerly, protein related to Dan and cerberus (PRDC)-is a potent antagonist of the bone morphogenetic proteins 2 and 4, but little else in known about its functions. We found that Grem2(-/-) mice developed small deformed mandibular and maxillary incisors, indicating that GREMLIN2 is required for normal tooth morphogenesis. Although DEXA scans suggested that bone mineral density might be increased in Grem2(-/-) mice, histology did not reveal any evident bone phenotype. Grem2(-/-) mice did not display any other notable phenotypes evaluated in a high-throughput screening process that encompassed a range of immunologic, metabolic, ophthalmic, and behavioral parameters. Our findings indicate that Grem2 can be added to the growing list of genes that affect tooth development in mice.

摘要

GREMLIN 2(GREM2)——以前称为与Dan和Cerberus相关的蛋白质(PRDC)——是骨形态发生蛋白2和4的强效拮抗剂,但对其功能了解甚少。我们发现Grem2基因敲除小鼠发育出小的畸形下颌和上颌切牙,这表明GREMLIN2是正常牙齿形态发生所必需的。尽管双能X线吸收法扫描表明Grem2基因敲除小鼠的骨矿物质密度可能增加,但组织学检查未发现任何明显的骨表型。在涵盖一系列免疫、代谢、眼科和行为参数的高通量筛选过程中,Grem2基因敲除小鼠未表现出任何其他显著的表型。我们的研究结果表明,Grem2可以添加到影响小鼠牙齿发育的不断增加的基因列表中。

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