## Abstract Craniosynostosis is a condition in which some or all of the sutures in the skull of an infant close prematurely. Fibroblast growth factor receptor 2 (FGFR2) mutations are a wellβknown cause of craniosynostosis. Many syndromes that comprise craniosynostosis, such as Apert syndrome, Crouz
A novel mutation in CD40 and its functional characterization
β Scribed by Chun-Jian Qi; Lu Zheng; Hong-Bing Ma; Min Fei; Ke-Qing Qian; Bai-Rong Shen; Chang-Ping Wu; Mauno Vihinen; Xue-Guang Zhang
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 613 KB
- Volume
- 30
- Category
- Article
- ISSN
- 1059-7794
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β¦ Synopsis
CD40 is a costimulatory protein expressed on the surface of many different cells. It delivers signals regulating diverse cellular responses, including proliferation, differentiation, growth suppression, and cell death. In this study, we report a novel CD40 mutant (c.234C>A or p.H78Q) that is expressed in the U266 cell line and in freshly isolated tumor cells. Three-dimensional structural model and Scatchard analysis revealed that the mutated residue located in a region is important for binding to CD40L (CD154). Functional analysis indicated that the mutated CD40 was translocated to the CD40 signalosome and involved in CD40 signal transduction. In conclusion, the mutation in CD40 can lead to an alteration of function, including the change of antigen epitope and the binding affinity with CD40L.
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Multiple endocrine neoplasia (MEN) syndromes are characterized by tumors involving two or more endocrine glands. Two MEN syndromes have long been known: MEN1 and MEN2, caused by germline mutations in __MEN1__ or __RET__, respectively. Recently, mutations in __CDKN1B__, encoding the cyclin-dependent