Quantitation of TGF-β proteins in mouse tissues shows reciprocal changes in TGF-β1 and TGF-β3 in normal vs neoplastic mammary epithelium

被引:23
作者
Flanders, Kathleen C. [1 ]
Yang, Yu-an [1 ]
Herrmann, Michelle [1 ]
Chen, JinQiu [1 ]
Mendoza, Nerissa [2 ]
Mirza, Amer M. [2 ]
Wakefield, Lalage M. [1 ]
机构
[1] NCI, Lab Canc Biol & Genet, Bethesda, MD 20892 USA
[2] Xoma Corp, Berkeley, CA 94710 USA
关键词
TGF-beta isoforms; protein; quantitation; mouse tissues; mammary gland; TRANSFORMING-GROWTH-FACTOR; INDUCED PULMONARY-FIBROSIS; BREAST-CANCER; IMMUNOHISTOCHEMICAL LOCALIZATION; GROWTH-FACTOR-BETA-1; GENE; EXPRESSION PATTERNS; TRANSGENIC MICE; MESSENGER-RNA; TUMOR; DISEASE;
D O I
10.18632/oncotarget.9416
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Transforming growth factor-beta s (TGF-beta s) regulate tissue homeostasis, and their expression is perturbed in many diseases. The three isoforms (TGF-beta 1, -beta 2, and -beta 3) have similar bioactivities in vitro but show distinct activities in vivo. Little quantitative information exists for expression of TGF-beta isoform proteins in physiology or disease. We developed an optimized method to quantitate protein levels of the three isoforms, using a Luminex (R) xMAP (R)-based multianalyte assay following acid-ethanol extraction of tissues. Analysis of multiple tissues and plasma from four strains of adult mice showed that TGF-beta 1 is the predominant isoform with TGF-beta 2 being similar to 10-fold lower. There were no sex-specific differences in isoform expression, but some tissues showed inter-strain variation, particularly for TGF-beta 2. The only adult tissue expressing appreciable TGF-beta 3 was the mammary gland, where its levels were comparable to TGF-beta 1. In situ hybridization showed the luminal epithelium as the major source of all TGF-beta isoforms in the normal mammary gland. TGF-beta 1 protein was 3-8-fold higher in three murine mammary tumor models than in normal mammary gland, while TGF-beta 3 protein was 2-3-fold lower in tumors than normal tissue, suggesting reciprocal regulation of these isoforms in mammary tumorigenesis.
引用
收藏
页码:38164 / 38179
页数:16
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