Pavelka M, Ellinger A
Eur J Cell Biol. 1983 Jan;29(2):253-61.
In the small intestine cell differentiation from immature crypt cells to mature absorptive cells localized along the villi is accompanied by alterations in the organization of the trans Golgi side. In immature crypt cells the transmost Golgi cisterna is usually located closely adjacent to the other cisternae thus being a component of the stack. Concomitantly with cell differentiation the transmost cisterna of an increasing number of Golgi stacks sets off from the other cisternae being then located at various distances to the stacks. This transmost cisterna has, as in several other cell types, been interpreted as "GERL" (Golgi associated endoplasmic reticulum lysosomes [20, 28]) and thus, has been postulated to represent a specialized region of the endoplasmic reticulum. Our results, however, have shown that the cytochemical staining pattern which has been used as a basis for the differentiation of GERL from Golgi components is not present in crypt cells nor in mature absorptive cells of the proximal small intestine: identical cisternae react for thiamine pyrophosphatase, inosine diphosphatase, and acid phosphatase. Thiamine pyrophosphatase and inosine diphosphatase--enzymes characteristic for Golgi cisternae--are apparent over transmost cisternae defined as GERL, too, and in addition, acid phosphatase--postulated as GERL-marker--is demonstrable over stacked Golgi cisternae. This overlapping cytochemical reaction, as well as the alterations during cell differentiation, indicate that those structures which have been described as GERL are to be interpreted as Golgi components rather than as endoplasmic reticulum. On the other hand, endoplasmic reticulum is a constant component of the trans Golgi face in undifferentiated crypt-base cells and in maturing cells of the crypt-top region. From its localization closely adjacent to trans Golgi cisternae it may be termed "Golgi-associated endoplasmic reticulum"; however, these cisternae of endoplasmic reticulum are constantly devoid of acid phosphatase. No indications exist for continuities with the thiamine pyrophosphatase-, inosine diphosphatase-, and acid phosphatase-positive transmost Golgi cisternae, and for an engagement in production of lysosomes.
在小肠中,从位于隐窝的未成熟细胞分化为沿绒毛分布的成熟吸收细胞的过程中,反式高尔基体侧的组织结构会发生改变。在未成熟的隐窝细胞中,最外侧的高尔基体潴泡通常紧邻其他潴泡,因此是高尔基体堆叠的一部分。随着细胞分化,越来越多的高尔基体堆叠中最外侧的潴泡与其他潴泡分离,然后与高尔基体堆叠保持不同距离。与其他几种细胞类型一样,这个最外侧的潴泡被解释为“GERL”(高尔基体相关的内质网溶酶体[20, 28]),因此被假定代表内质网的一个特殊区域。然而,我们的结果表明,用于区分GERL和高尔基体成分的细胞化学染色模式在隐窝细胞和近端小肠的成熟吸收细胞中均不存在:相同的潴泡对硫胺素焦磷酸酶、肌苷二磷酸酶和酸性磷酸酶均有反应。硫胺素焦磷酸酶和肌苷二磷酸酶——高尔基体潴泡的特征性酶——在被定义为GERL的最外侧潴泡上也很明显,此外,被假定为GERL标志物的酸性磷酸酶在堆叠的高尔基体潴泡上也可检测到。这种重叠的细胞化学反应以及细胞分化过程中的变化表明,那些被描述为GERL的结构应被解释为高尔基体成分而非内质网。另一方面,内质网是未分化的隐窝底部细胞和隐窝顶部区域成熟细胞中反式高尔基体面的一个恒定成分。由于其紧邻反式高尔基体潴泡的定位,它可被称为“高尔基体相关内质网”;然而,这些内质网潴泡始终缺乏酸性磷酸酶。没有迹象表明其与硫胺素焦磷酸酶、肌苷二磷酸酶和酸性磷酸酶阳性的最外侧高尔基体潴泡有连续性,也没有迹象表明其参与溶酶体的产生。