Stein Torsten, Morris Joanna S, Davies Claire R, Weber-Hall Stephen J, Duffy Marie-Anne, Heath Victoria J, Bell Alexandra K, Ferrier Roderick K, Sandilands Gavin P, Gusterson Barry A
Division of Cancer Sciences and Molecular Pathology, Western Infirmary, Glasgow, UK.
Breast Cancer Res. 2004;6(2):R75-91. doi: 10.1186/bcr753. Epub 2003 Dec 18.
Involution of the mammary gland is a complex process of controlled apoptosis and tissue remodelling. The aim of the project was to identify genes that are specifically involved in this process.
We used Affymetrix oligonucleotide microarrays to perform a detailed transcript analysis on the mechanism of controlled involution after withdrawal of the pups at day seven of lactation. Some of the results were confirmed by semi-quantitative reverse transcriptase polymerase chain reaction, Western blotting or immunohistochemistry.
We identified 145 genes that were specifically upregulated during the first 4 days of involution; of these, 49 encoded immunoglobulin genes. A further 12 genes, including those encoding the signal transducer and activator of transcription 3 (STAT3), the lipopolysaccharide receptor (CD14) and lipopolysaccharide-binding protein (LBP), were involved in the acute-phase response, demonstrating that the expression of acute-phase response genes can occur in the mammary gland itself and not only in the liver. Expression of LBP and CD14 was upregulated, at both the RNA and protein level, immediately after pup withdrawal; CD14 was strongly expressed in the luminal epithelial cells. Other genes identified suggested neutrophil activation early in involution, followed by macrophage activation late in the process. Immunohistochemistry and histological staining confirmed the infiltration of the involuting mammary tissue with neutrophils, plasma cells, macrophages and eosinophils.
Oligonucleotide microarrays are a useful tool for identifying genes that are involved in the complex developmental process of mammary gland involution. The genes identified are consistent with an immune cascade, with an early acute-phase response that occurs in the mammary gland itself and resembles a wound healing process.
乳腺退化是一个涉及可控性细胞凋亡和组织重塑的复杂过程。本项目的目的是鉴定特异性参与此过程的基因。
我们使用Affymetrix寡核苷酸微阵列,对哺乳期第7天幼崽断奶后可控性退化机制进行详细的转录分析。部分结果通过半定量逆转录聚合酶链反应、蛋白质免疫印迹或免疫组织化学得以证实。
我们鉴定出145个在退化的前4天特异性上调的基因;其中,49个编码免疫球蛋白基因。另外12个基因,包括编码信号转导及转录激活因子3(STAT3)、脂多糖受体(CD14)和脂多糖结合蛋白(LBP)的基因,参与急性期反应,表明急性期反应基因的表达不仅可发生于肝脏,也可在乳腺自身出现。幼崽断奶后,LBP和CD14的RNA及蛋白质水平均立即上调;CD14在腔上皮细胞中强烈表达。鉴定出的其他基因提示退化早期中性粒细胞被激活,随后在此过程后期巨噬细胞被激活。免疫组织化学和组织学染色证实退化的乳腺组织中有中性粒细胞、浆细胞、巨噬细胞和嗜酸性粒细胞浸润。
寡核苷酸微阵列是鉴定参与乳腺退化复杂发育过程基因的有用工具。鉴定出的基因与免疫级联反应一致,乳腺自身会出现早期急性期反应,类似于伤口愈合过程。