Kiyozumi Daiji, Sugimoto Nagisa, Nakano Itsuko, Sekiguchi Kiyotoshi
Laboratory of Extracellular Matrix Biochemistry, Institute for Protein Research, Osaka University, Suita, Osaka, 565-0871, Japan.
Matrix Biol. 2007 Jul;26(6):456-62. doi: 10.1016/j.matbio.2007.03.001. Epub 2007 Mar 30.
A novel protein family characterized by the presence of 12 CSPG repeats and Calx-beta domains includes Fras1, QBRICK/Frem1, Frem2 and Frem3. Although Fras1, QBRICK/Frem1 and Frem2 have been shown to localize at the basement membrane through reciprocal stabilization, it remains unclear whether Frem3 is also deposited at the basement membrane in a similar manner. Here we show that Frem3 localizes at the basement membrane with tissue distribution patterns clearly distinct from those of other 12 CSPG repeats-containing proteins (12-CSPG proteins). In adult mice, Frem3 was present at the basement membrane underlying ductal cells of the salivary gland, retinal ganglion cells, basal cells of epidermis and hair follicles, where other 12-CSPG proteins were barely expressed. In embryos and neonates, the expression of Frem3 transcripts was significantly lower than that of the other 12-CSPG proteins, although Frem3 protein was coexpressed with other 12-CSPG proteins at the basement membranes of retina, renal epithelia and epidermis. Interestingly, Frem3 deposition at the epidermal basement membrane was not severely compromised in blebbing mutant embryos, in which the basement membrane deposition of other 12-CSPG proteins was dramatically reduced due to the breakdown of their reciprocal stabilization. These results indicate that Frem3 is a basement membrane protein that is distinct from other 12-CSPG proteins in its tissue distribution and competence to assemble into the basement membrane.
一个以存在12个硫酸软骨素蛋白聚糖(CSPG)重复序列和钙结合蛋白β(Calx-beta)结构域为特征的新型蛋白质家族包括Fras1、QBRICK/Frem1、Frem2和Frem3。尽管Fras1、QBRICK/Frem1和Frem2已被证明通过相互稳定作用定位于基底膜,但Frem3是否也以类似方式沉积在基底膜上仍不清楚。在此我们表明,Frem3定位于基底膜,其组织分布模式与其他含12个CSPG重复序列的蛋白质(12-CSPG蛋白质)明显不同。在成年小鼠中,Frem3存在于唾液腺导管细胞、视网膜神经节细胞、表皮基底细胞和毛囊下方的基底膜,而其他12-CSPG蛋白质在这些部位几乎不表达。在胚胎和新生儿中,Frem3转录本的表达明显低于其他12-CSPG蛋白质,尽管Frem3蛋白与其他12-CSPG蛋白质在视网膜、肾上皮和表皮的基底膜共表达。有趣的是,在泡状突变胚胎中,Frem3在表皮基底膜的沉积并未受到严重影响,在这种突变胚胎中,由于其他12-CSPG蛋白质相互稳定作用的破坏,它们在基底膜的沉积显著减少。这些结果表明,Frem3是一种基底膜蛋白,其在组织分布和组装到基底膜的能力方面与其他12-CSPG蛋白质不同。