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地塞米松、表皮生长因子和视黄酸对原代培养大鼠下颌下腺腺泡-闰管复合体的影响。

Effects of dexamethasone, epidermal growth factor, and retinoic acid on rat submandibular acinar-intercalated duct complexes in primary culture.

作者信息

Redman R S, Quissell D O, Barzen K A

机构信息

Oral Pathology Research Laboratory, Veterans Administration Medical Center, Washington, DC 20422.

出版信息

In Vitro Cell Dev Biol. 1988 Aug;24(8):734-42. doi: 10.1007/BF02623642.

Abstract

Mature acini with attached segments of intercalated ducts were dissociated from the submandibular glands of rats and grown in primary culture on gels of reconstituted rat tail collagen. Screening evaluations indicated that the following new conditions promoted a substantial improvement in the survival of the cells as compared with our previously reported results: a) adding dexamethasone, epidermal growth factor, and retinoic acid to the medium, b) decreasing the fetal bovine serum in the medium to 1%; and c) adjusting the oxygen in the gas phase to 50%. A detailed evaluation, including light and electron microscopy and biochemical analysis, then provided the following observations. The acinar-ductal complexes enlarged throughout the 22-d culture period, and after 4 d sheets comprised of a one- to two-cell thick layer of acinar cells spread among the complexes. Synthesis of mucin, and its secretion in response to norepinephrine or cAMP, dropped precipitously to very low levels after 2 d. However, synthesis of DNA, general proteins, and glycoproteins dropped only transiently after 2 d, rising to levels approaching those of freshly dissociated complexes by 22 d. These data indicate that a shift occurred from the synthesis of large quantities of secretory proteins and glycoproteins, especially mucins, during the first 2 d in culture, to other materials thereafter. Overall, the new culture conditions resulted in substantial growth and survival of acinar cells through 22 d in primary culture, but the important acinar characteristic of the synthesis and secretion of mucins was essentially lost after 4 d.

摘要

将带有闰管附着段的成熟腺泡从大鼠下颌下腺中分离出来,在重组大鼠尾胶原凝胶上进行原代培养。筛选评估表明,与我们之前报道的结果相比,以下新条件可显著提高细胞存活率:a)在培养基中添加地塞米松、表皮生长因子和视黄酸;b)将培养基中的胎牛血清浓度降至1%;c)将气相中的氧气浓度调整至50%。随后进行的详细评估,包括光镜和电镜观察以及生化分析,得出了以下观察结果。在整个22天的培养期内,腺泡-导管复合体不断增大,4天后,由一到两层细胞厚的腺泡细胞层组成的薄片在复合体之间扩散。培养2天后,粘蛋白的合成及其对去甲肾上腺素或cAMP的分泌急剧下降至极低水平。然而,DNA、总蛋白和糖蛋白的合成在2天后仅短暂下降,到22天时回升至接近刚分离的复合体的水平。这些数据表明,在培养的前2天,细胞从大量合成分泌蛋白和糖蛋白,尤其是粘蛋白,转变为之后合成其他物质。总体而言,新的培养条件使腺泡细胞在原代培养的22天内实现了显著生长和存活,但粘蛋白合成和分泌这一重要的腺泡特征在4天后基本丧失。

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