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小鼠下颌下腺中表皮生长因子mRNA的原位定位

In situ localization of mRNA for epidermal growth factor in the submandibular gland of the mouse.

作者信息

Gresik E W, Gubits R M, Barka T

出版信息

J Histochem Cytochem. 1985 Dec;33(12):1235-40. doi: 10.1177/33.12.3877752.

Abstract

Epidermal growth factor (EGF) is a polypeptide originally isolated from the mouse submandibular gland, where it is localized immunocytochemically in cells of the granular convoluted tubules (GCT). cDNAs encoding the precursor of mouse submandibular EGF have been cloned (Scott et al. Science 221:236, 1983; Gray et al. Nature 303:722, 1983). A fragment of one of these clones, pmegf10, containing the EGF coding region, was tritium-labeled by nick-translation and used as a probe for in situ hybridization to EGF mRNA. A specific hybridization signal for EGF mRNA was seen only in mature or developing GCT cells. The intensity of the signal was stronger in glands of intact males than in females or in castrated males. In glands of castrates treated with testosterone, or of intact females treated with triiodothyronine (T3), the signal was comparable to that in intact males. In glands of males treated with T3 the intensity of the signal was stronger than in untreated males. A weak to moderate signal was seen in developing GCT cells of 20-day-old males but not females. Hybridization for 3 days gave a stronger signal than that for 1 day. No signal was seen in either sex at 10 days of age, or in control preparations exposed to labeled DNA of pBR322. The presence of EGF mRNA exclusively in GCT cells provides strong evidence that these cells are the only site of synthesis of EGF in the submandibular gland. In situ hybridization with this cDNA probe will provide a sensitive method to determine possible cellular sites of EGF production outside of the submandibular gland.

摘要

表皮生长因子(EGF)是最初从小鼠颌下腺分离出来的一种多肽,通过免疫细胞化学方法发现它定位于颗粒曲管(GCT)细胞中。编码小鼠颌下EGF前体的cDNA已被克隆(斯科特等人,《科学》221:236,1983;格雷等人,《自然》303:722,1983)。其中一个克隆pmegf10的片段,包含EGF编码区,通过切口平移法用氚标记,并用作原位杂交检测EGF mRNA的探针。仅在成熟或发育中的GCT细胞中观察到EGF mRNA的特异性杂交信号。完整雄性腺体中的信号强度比雌性或去势雄性腺体中的更强。在用睾酮处理的去势动物腺体或用三碘甲状腺原氨酸(T3)处理的完整雌性腺体中,信号与完整雄性腺体中的相当。在用T3处理的雄性腺体中,信号强度比未处理的雄性更强。在20日龄雄性而非雌性的发育中的GCT细胞中观察到弱至中等强度的信号。杂交3天产生的信号比杂交1天更强。在10日龄的两性动物中或在暴露于pBR322标记DNA的对照制剂中均未观察到信号。EGF mRNA仅存在于GCT细胞中,这有力地证明了这些细胞是颌下腺中EGF的唯一合成部位。用该cDNA探针进行原位杂交将提供一种灵敏的方法来确定颌下腺以外可能产生EGF的细胞部位。

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