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大鼠腮腺发育过程中的分泌蛋白表达模式。

Secretory protein expression patterns during rat parotid gland development.

作者信息

Sivakumar S, Mirels L, Miranda A J, Hand A R

机构信息

Department of Pediatric Dentistry, University of Connecticut Health Center, Farmington 06030, USA.

出版信息

Anat Rec. 1998 Nov;252(3):485-97. doi: 10.1002/(SICI)1097-0185(199811)252:3<485::AID-AR17>3.0.CO;2-J.

Abstract

The rat parotid gland produces a number of well-characterized secretory proteins. Relatively little is known, however, about the onset of their synthesis and cellular localization during gland development. Secretory protein expression was studied in parotid glands of fetal and postnatal rats using light and electron microscopic immunocytochemistry and Northern blotting. Amylase, parotid secretory protein (PSP), common salivary protein-1 (CSP-1), and SMGB were first detected by immunofluorescence in parotid glands of 18 day fetuses. By 5 days after birth, light and electron microscopic immunolabeling localized all of these proteins to the secretory granules of developing acinar cells. Labeling of acinar cells for DNAse I, however, was not observed until 18 days after birth. Between 9 and 25 days, CSP-1 and SMGB reactivity of acinar cells declined, but increased in intercalated duct cells. After 25 days, CSP-1 and SMGB were found only in intercalated ducts, and amylase, PSP, and DNAse I were restricted to acinar cells. Levels of CSP-1 and SMGB mRNA were relatively constant through 21 postnatal days, but declined significantly after that. Amylase and PSP mRNA increased rapidly and continuously from five days after birth to the adult stage. In contrast, DNAse I mRNA was not detectable until 18 days after birth. The immunocytochemical and molecular analyses define three basic patterns of protein expression in the rat parotid gland: proteins whose synthesis is initiated early in development and is maintained in the acinar cells, such as amylase and PSP; proteins that are initially synthesized by immature acinar cells but are restricted to intercalated ducts in the adult gland, such as CSP-1 and SMGB; and proteins that are synthesized only by mature acinar cells and first appear during the third postnatal week, such as DNAse I. The parotid gland exhibits four distinct developmental stages: prenatal, from initiation of the gland rudiment until birth; neonatal, from 1 day up to about 9 days postnatal; transitional, from 9 days to 25 days of age; and adult, from 25 days on. Although differences exist in timing and in the specific proteins expressed, these developmental stages are similar to those seen in the rat submandibular gland. Additionally, the results support the suggestion that intercalated ducts may differentiate from the neonatal acini.

摘要

大鼠腮腺能产生多种特性明确的分泌蛋白。然而,对于这些蛋白在腺体发育过程中的合成起始及细胞定位,人们了解得相对较少。利用光镜和电镜免疫细胞化学以及Northern印迹法,对胎鼠和新生大鼠的腮腺分泌蛋白表达进行了研究。淀粉酶、腮腺分泌蛋白(PSP)、常见唾液蛋白-1(CSP-1)和SMGB首先在18日龄胎儿的腮腺中通过免疫荧光检测到。出生后5天,光镜和电镜免疫标记将所有这些蛋白定位到发育中的腺泡细胞的分泌颗粒中。然而,直到出生后18天,才观察到腺泡细胞对DNA酶I的标记。在9至25天之间,腺泡细胞的CSP-1和SMGB反应性下降,但闰管细胞中的反应性增加。25天后,CSP-1和SMGB仅在闰管中发现,而淀粉酶、PSP和DNA酶I则局限于腺泡细胞。CSP-1和SMGB mRNA水平在出生后21天内相对恒定,但之后显著下降。淀粉酶和PSP mRNA从出生后5天到成年阶段迅速且持续增加。相比之下,DNA酶I mRNA直到出生后18天才可检测到。免疫细胞化学和分子分析确定了大鼠腮腺中三种基本的蛋白表达模式:在发育早期开始合成并在腺泡细胞中持续表达的蛋白,如淀粉酶和PSP;最初由未成熟腺泡细胞合成但在成年腺体中局限于闰管的蛋白,如CSP-1和SMGB;以及仅由成熟腺泡细胞合成且在出生后第三周首次出现的蛋白,如DNA酶I。腮腺呈现出四个不同的发育阶段:产前阶段,从腺体原基开始形成到出生;新生儿阶段,从出生后1天到约9天;过渡阶段,从9天到25天;成年阶段,从25天开始。尽管在时间和所表达的特定蛋白方面存在差异,但这些发育阶段与大鼠下颌下腺的相似。此外,结果支持闰管可能从新生儿腺泡分化而来的观点。

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