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乳腺发育的关键阶段:作为运动器官的乳腺终末芽

Key stages in mammary gland development: the mammary end bud as a motile organ.

作者信息

Hinck Lindsay, Silberstein Gary B

机构信息

Sinsheimer Laboratories, Department of Cell, Molecular and Developmental Biology, University of California, Santa Cruz, Santa Cruz, CA 95064, USA.

出版信息

Breast Cancer Res. 2005;7(6):245-51. doi: 10.1186/bcr1331. Epub 2005 Oct 3.

Abstract

In the rodent, epithelial end buds define the tips of elongating mammary ducts. These highly motile structures undergo repeated dichotomous branching as they aggressively advance through fatty stroma and, turning to avoid other ducts, they finally cease growth leaving behind the open, tree-like framework on which secretory alveoli develop during pregnancy. This review identifies the motility of end buds as a unique developmental marker that represents the successful integration of systemic and local mammotrophic influences, and covers relevant advances in ductal growth regulation, extracellular matrix (ECM) remodeling, and cell adhesion in the inner end bud. An unexpected growth-promoting synergy between insulin-like growth factor-1 and progesterone, in which ducts elongate without forming new end buds, is described as well as evidence strongly supporting self-inhibition of ductal elongation by end-bud-secreted transforming growth factor-beta acting on stromal targets. The influence of the matrix metalloproteinase ECM-remodeling enzymes, notably matrix metalloproteinase-2, on end bud growth is discussed in the broader context of enzymes that regulate the polysaccharide-rich glycosaminoglycan elements of the ECM. Finally, a critical, motility-enabling role for the cellular architecture of the end bud is identified and the contribution of cadherins, the netrin/neogenin system, and ErbB2 to the structure and motility of end buds is discussed.

摘要

在啮齿动物中,上皮终末芽定义了伸长的乳腺导管的末端。这些高度可移动的结构在积极穿过脂肪基质时经历反复的二叉分支,并且为避开其他导管而转向,最终停止生长,留下开放的树状框架,在怀孕期间分泌性肺泡在该框架上发育。本综述将终末芽的移动性确定为一种独特的发育标志物,它代表了全身和局部乳腺营养影响的成功整合,并涵盖了导管生长调节、细胞外基质(ECM)重塑以及内终末芽中细胞粘附方面的相关进展。描述了胰岛素样生长因子-1和孕酮之间意想不到的促生长协同作用,即导管伸长但不形成新的终末芽,以及有力证据支持终末芽分泌的转化生长因子-β作用于基质靶点对导管伸长的自我抑制。在调节富含多糖的糖胺聚糖成分的ECM的酶的更广泛背景下,讨论了基质金属蛋白酶ECM重塑酶,特别是基质金属蛋白酶-2对终末芽生长的影响。最后,确定了终末芽细胞结构在移动性方面的关键作用,并讨论了钙黏着蛋白、网蛋白/新生成蛋白系统和ErbB2对终末芽结构和移动性的贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e7b/1410762/391d418f41bd/bcr1331-1.jpg

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