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来自癌前乳腺增生的上皮细胞对乳腺脂肪组织的反应性生长。

Growth of epithelium from a preneoplastic mammary outgrowth in response to mammary adipose tissue.

作者信息

Beck J C, Hosick H L, Watkins B A

机构信息

Department of Zoology, Washington State University, Pullman 99164.

出版信息

In Vitro Cell Dev Biol. 1989 May;25(5):409-18. doi: 10.1007/BF02624625.

Abstract

We investigated the effects of conditioned media derived from mouse mammary fat pads on the proliferation of CL-S1 cells, an epithelial cell line originally isolated from a preneoplastic mammary outgrowth line. Cell proliferation in vitro in serum-free defined medium was compared to that in this medium conditioned using intact mammary fat pad pieces or isolated fat pad adipocytes. Culture medium was conditioned by incubating the conditioning material in defined culture medium for 24 h at 37 degrees C. Conditioned medium induced CL-S1 proliferation as much as 10- to 20-fold above the minimal levels of growth in control cultures after 13 d of culture. The growth-stimulatory factor(s) had an apparent molecular weight of greater than 10 kDa. This growth-stimulatory activity was both heat and trypsin stable. Because the role of adipose tissue is to store and release lipids, we next tested whether lipids are released during medium conditioning. The lipid composition of the fat pad conditioned medium was characterized using both thin layer and gas liquid chromatography. These lipid analyses indicated that the fat pad pieces released significant amounts of fatty acids and phospholipids into the medium during the conditioning period. The free fatty acid composition included both saturated and unsaturated molecules, and about 80% of the total fatty acids consisted of palmitate, stearate, oleate, and linoleate. These same fatty acids were a structural component of the majority of phospholipid found in the medium. The addition of palmitate or stearate to defined medium had no effect or was inhibitory for CL-S1 proliferation, depending on the concentration used. Defined medium supplemented with oleate, arachidonate, or linoleate induced CL-S1 proliferation, and the inhibitory effects of palmitate and stearate were overcome by addition of oleate and linoleate. These data indicate that both unsaturated and saturated fatty acids are released from intact adipose cells of the mouse mammary fat pad and that fatty acids can influence the growth of preneoplastic mouse mammary epithelium. Thus, unsaturated fatty acids, perhaps in conjunction with other substances released simultaneously, are candidate molecules for the substances that mediate the effect of adipose tissue on growth of epithelium.

摘要

我们研究了源自小鼠乳腺脂肪垫的条件培养基对CL-S1细胞增殖的影响,CL-S1细胞系是一种最初从癌前乳腺增生系中分离出的上皮细胞系。将无血清限定培养基中的体外细胞增殖与使用完整乳腺脂肪垫碎片或分离的脂肪垫脂肪细胞处理后的该培养基中的细胞增殖进行比较。通过在限定培养基中于37℃孵育处理材料24小时来制备条件培养基。培养13天后,条件培养基诱导CL-S1细胞增殖比对照培养物中的最低生长水平高10至20倍。生长刺激因子的表观分子量大于10 kDa。这种生长刺激活性对热和胰蛋白酶均稳定。由于脂肪组织的作用是储存和释放脂质,我们接下来测试了在培养基制备过程中是否会释放脂质。使用薄层色谱法和气液色谱法对脂肪垫条件培养基的脂质组成进行了表征。这些脂质分析表明,在制备期间,脂肪垫碎片向培养基中释放了大量脂肪酸和磷脂。游离脂肪酸组成包括饱和和不饱和分子,总脂肪酸的约80%由棕榈酸、硬脂酸、油酸和亚油酸组成。这些相同的脂肪酸是培养基中发现的大多数磷脂的结构成分。向限定培养基中添加棕榈酸或硬脂酸对CL-S1细胞增殖没有影响或具有抑制作用,这取决于所使用的浓度。添加油酸、花生四烯酸或亚油酸的限定培养基诱导CL-S1细胞增殖,并且添加油酸和亚油酸可克服棕榈酸和硬脂酸的抑制作用。这些数据表明,不饱和脂肪酸和饱和脂肪酸均从小鼠乳腺脂肪垫的完整脂肪细胞中释放出来,并且脂肪酸可以影响癌前小鼠乳腺上皮的生长。因此,不饱和脂肪酸,可能与同时释放的其他物质一起,是介导脂肪组织对上皮生长影响的物质的候选分子。

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