首页> 外文期刊>Journal of Morphology >Immunolocalization of keratin-associated beta-proteins (beta-keratins) in the regenerating lizard epidermis indicates a new process for the differentiation of the epidermis in lepidosaurians
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Immunolocalization of keratin-associated beta-proteins (beta-keratins) in the regenerating lizard epidermis indicates a new process for the differentiation of the epidermis in lepidosaurians

机译:再生蜥蜴表皮中与角蛋白相关的β蛋白(β-角蛋白)的免疫定位表明鳞状龙的表皮分化的新过程。

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The process of keratinocyte differentiation was analyzed in the regenerating epidermis of the lizard Anolis carolinensis, where the genes coding for beta-proteins (beta-keratins) are known. The regenerating epidermis forms all epidermal layers found in normal scales (Oberh?utchen-, beta-, mesos-, and alpha-layer). Three specific proteins representing the larger families of beta-proteins, glycine-rich (HgG5, 28% glycine, 3.6% cysteine), glycine-cysteine medium-rich (HgGC10, 13% glycine, 14.5% cysteine), and glycine-cysteine rich (HgGC3, 30.4% glycine, 8.7% cysteine) have been immunolocalized at the ultrastructural level. HgG5 is only present in differentiating beta-cells, a weak or no labeling is observed in Oberh?utchen and is absent in alpha-cells. The protein is located in the pale corneous material forming the compact beta-layer but is absent in mature Oberh?utchen cells. HgGC10 is present among beta-packets in Oberh?utchen and beta-cells but disappears in more compact and electron-pale corneous material. The labeling disappears in mesos-cells and is present with variable intensity in alpha-cells, whereas lacunar and clear-cells are low labeled to unlabeled. HgGC3 is sparse or absent in beta-cells but is lightly present in the darker corneous material of differentiating and mature alpha-cells, lacunar-cells, and clear-cells. The study suggests that while glycine-rich proteins (electron-pale) are specifically used for building the resistant and hydrophobic beta-layer, cysteine-glycine rich proteins (electron-denser) are used to form the pliable corneous material present in the Oberh?utchen and alpha-cells. The differential accumulation of beta-proteins on the alpha-keratin cytoskeleton scaffold and not the alternance of beta- with alpha-keratins allow the differentiation of different epidermal layers.
机译:在蜥蜴Anolis carolinensis的再生表皮中分析了角质形成细胞的分化过程,其中已知编码β蛋白(β-角蛋白)的基因。再生的表皮形成正常规模的所有表皮层(Oberh?utchen,β,mesos和α层)。代表更大的β蛋白家族的三种特定蛋白质,富含甘氨酸的蛋白(HgG5、28%甘氨酸,3.6%半胱氨酸),富含甘氨酸-半胱氨酸的培养基(HgGC10、13%甘氨酸,14.5%半胱氨酸)和富含甘氨酸-半胱氨酸(HgGC3、30.4%甘氨酸,8.7%半胱氨酸)已在超微结构水平进行了免疫定位。 HgG5仅存在于分化的β细胞中,在Oberh?utchen中观察到的标记很弱或没有,而在α细胞中则没有。该蛋白质位于形成紧密的β层的浅色角质层中,但在成熟的Oberh?utchen细胞中不存在。 HgGC10存在于Oberh?utchen的beta包和beta细胞中,但消失在更紧凑和电子苍白的角质材料中。标记在中胚层细胞中消失,并在α细胞中以可变的强度存在,而腔隙和透明细胞的标记程度低至未标记。 HgGC3在β细胞中稀疏或不存在,但在分化和成熟的α细胞,腔隙细胞和透明细胞的深色角质物质中轻度存在。研究表明,虽然富含甘氨酸的蛋白质(电子苍白)专门用于构建抗性和疏水性β层,但富含半胱氨酸-甘氨酸的蛋白质(电子登革热)用于形成Oberh?中存在的柔韧的角质材料。 utchen和alpha单元。 β-蛋白在α-角蛋白细胞骨架支架上的差异积累,而不是β-与α-角蛋白的交替差异,可以区分不同的表皮层。

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