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发育中的切牙中Col1a1 - GFP转基因的表达。

Col1a1-GFP transgene expression in developing incisors.

作者信息

Braut A, Kalajzic I, Kalajzic Z, Rowe D W, Kollar E J, Mina M

机构信息

Department of Pediatric Dentistry, University of Connecticut Health Center, Farmington, Connecticut, USA.

出版信息

Connect Tissue Res. 2002;43(2-3):216-9. doi: 10.1080/03008200290001078.

Abstract

Previous studies have shown that terminal differentiation of odontoblasts is accompanied by dramatic increases in type I collagen synthesis. Recently transgenic mice in which green fluorescent protein (GFP) expression is under the control of the rat 3.6 (pOBCol3.6GFPtpz) and 2.3 (pOBCol2.3GFPemd) Col1a1 promoter fragments were generated. Our analysis of these GFP-expressing transgenic mice shows that the 2.3-kb promoter fragment directs strong expression of GFP only to bones and teeth, whereas the 3.6-kb fragment of promoter directs strong expression of GFP in bone and tooth, as well as in other type I collagen producing tissues. Our observations of incisors in these transgenic mice show high levels of GFP expression in functional odontoblasts and in differentiated osteoblasts. These observations show that expression of GFP reporter genes closely follow the patterns of expression of alpha 1(I) collagen in various tissues including odontoblasts.

摘要

先前的研究表明,成牙本质细胞的终末分化伴随着I型胶原合成的显著增加。最近,构建了绿色荧光蛋白(GFP)表达受大鼠3.6(pOBCol3.6GFPtpz)和2.3(pOBCol2.3GFPemd)Col1a1启动子片段控制的转基因小鼠。我们对这些表达GFP的转基因小鼠的分析表明,2.3 kb的启动子片段仅将GFP的强表达导向骨骼和牙齿,而3.6 kb的启动子片段则将GFP的强表达导向骨骼、牙齿以及其他产生I型胶原的组织。我们对这些转基因小鼠切牙的观察显示,功能性成牙本质细胞和分化的成骨细胞中GFP表达水平很高。这些观察结果表明,GFP报告基因的表达与α1(I)胶原在包括成牙本质细胞在内的各种组织中的表达模式密切相关。

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