Durban E M, Knepper J E, Medina D, Butel J S
Oral Diagnostic Sciences Department, University of Texas Dental Branch, Houston.
Virus Res. 1990 Jul;16(3):307-23. doi: 10.1016/0168-1702(90)90055-g.
The interactions between differentiation-associated cellular events in the intact mammary gland or in cultured mammary cells and the post-transcriptional activity of the endogenous mouse mammary tumor virus (MMTV) loci were investigated. The transcriptional activities of the endogenous MMTV proviruses of the BALB/c mouse strain (Mtv-6, Mtv-8 and Mtv-9) appear to be regulated differentially during pregnancy-induced mammary gland development (J.E. Knepper, D. Medina and J.S. Butel, J. Virol. 59, 518-521, 1986). Analysis of MMTV-specific proteins at various stages of mammary gland development (virgin, midpregnant, lactating, regressing) established the presence of steady-state levels of a 67,000-Mr env precursor-type polypeptide at all physiological stages. However, processing to lower-molecular-weight env-specific proteins, including a predominant 50,000-Mr species, was detected only with the transition to the functional mammary gland phenotype. The contributions of cell proliferation, cell-matrix interactions, and modulation of functional activity to the pattern of endogenous MMTV protein expression were investigated using a 3-dimensional collagen type I culture system. Growth and cell-matrix interactions (cell polarization, lumen formation) leading to formation of 3-dimensional duct-like structures were permissive for the synthesis and processing of MMTV-specific proteins; accumulation of high levels of the 50,000-Mr env-specific polypeptide was associated with the onset of the fully functional mammary cell phenotype. Expression of MMTV-specific proteins was not due to amplification of a specific cell subpopulation. The potential of the full-length Mtv-8 and Mtv-9 proviruses to be transcribed, as indicated by their methylation status, was not dramatically different between differentiated and undifferentiated mammary cells in culture. This study indicates that MMTV transcriptional activity is reflected at the protein level in mammary tissue of BALB/c mice and that viral protein synthesis and processing may serve as important markers of different physiological stages of mammary epithelial cells. These observations also suggest a general approach to the examination of potential modulatory effects of cellular interactions (cell-cell, cell-matrix or both) known to be important in various differentiated epithelial cell systems for the expression of viral genes.
研究了完整乳腺或培养乳腺细胞中与分化相关的细胞事件与内源性小鼠乳腺肿瘤病毒(MMTV)基因座转录后活性之间的相互作用。BALB/c小鼠品系的内源性MMTV前病毒(Mtv-6、Mtv-8和Mtv-9)的转录活性在妊娠诱导的乳腺发育过程中似乎受到不同的调节(J.E. Knepper、D. Medina和J.S. Butel,《病毒学杂志》59,518 - 521,1986)。对乳腺发育不同阶段(处女期、妊娠中期、哺乳期、退化期)的MMTV特异性蛋白进行分析,发现在所有生理阶段均存在稳态水平的67,000道尔顿的env前体类型多肽。然而,只有在向功能性乳腺表型转变时,才检测到加工成低分子量env特异性蛋白,包括主要的50,000道尔顿物种。使用三维I型胶原培养系统研究了细胞增殖、细胞 - 基质相互作用以及功能活性调节对内源性MMTV蛋白表达模式的影响。导致三维导管样结构形成的生长和细胞 - 基质相互作用(细胞极化、管腔形成)有利于MMTV特异性蛋白的合成和加工;高水平的50,000道尔顿env特异性多肽的积累与完全功能性乳腺细胞表型的出现相关。MMTV特异性蛋白的表达不是由于特定细胞亚群的扩增。全长Mtv-8和Mtv-9前病毒转录的潜力,如通过其甲基化状态所示,在培养的分化和未分化乳腺细胞之间没有显著差异。这项研究表明,MMTV转录活性在BALB/c小鼠乳腺组织的蛋白质水平上得到反映,并且病毒蛋白的合成和加工可能是乳腺上皮细胞不同生理阶段的重要标志物。这些观察结果还提出了一种通用方法,用于检查已知在各种分化上皮细胞系统中对病毒基因表达重要的细胞相互作用(细胞 - 细胞、细胞 - 基质或两者)的潜在调节作用。