D2.0R雌性BALB/c小鼠D2乳腺增生性肺泡结节肿瘤细胞株mouse) breast cancer cell liine BioVector NTCC®典型培养物保藏中心
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- 货 号:NTCC®-D2.0
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NTCC® D2.0R细胞系(或称 D2OR,Cellosaurus登录号CVCL_0I88)是一种鼠源(小鼠)乳腺癌细胞模型,在癌症研究中被广泛用于研究肿瘤休眠和转移复发。它通常与相关的、高增殖性的D2A1细胞系进行比较研究。
起源: D2.0R细胞源自雌性BALB/c小鼠的D2乳腺增生性肺泡结节肿瘤,但其建系来源的肿瘤不易形成自发性转移。
表型: 它的特点是在特定的微环境(体内和体外)中表现出休眠或静止表型。这些细胞可以以单个非增殖细胞的状态长期存活,然后在特定条件下重新激活并形成转移灶。

研究用途: 该细胞系对于研究控制肿瘤从休眠状态转变为侵袭性、增殖性转移生长的机制至关重要。研究人员利用它来探讨细胞外基质(ECM)成分(如I型胶原蛋白可诱导增殖)和免疫系统(如自然杀伤细胞在维持休眠中起关键作用)在调节休眠中的作用。
休眠标志物: 休眠的D2.0R细胞通常表达较低水平的增殖标志物Ki-67、磷酸化ERK,而表达较高水平的p38以及休眠相关基因,如Cfh和Gas6。ERK/p38活性的比例被认为是判断细胞增殖或休眠状态的关键指标。
培养条件: 在使用基底膜提取物(BME)基质的标准3D培养系统中,D2.0R细胞通常保持静止(休眠)状态,而D2A1细胞则会增殖。
D2.0R模型已证实,使用针对活跃增殖细胞的常规化疗可能会“放过”非分裂的休眠癌细胞,而这些细胞正是后期转移的根源。这强调了开发专门针对休眠细胞的治疗方法的重要性。自体吞噬(Autophagy,又称细胞自噬)被发现是促进休眠D2.0R细胞存活的关键机制之一。
Origin: The D2.0R cells were derived from a D2 hyperplastic alveolar nodule mammary tumor in a female BALB/c mouse, but were established from a tumor that did not readily form spontaneous metastases.
Phenotype: They are characterized by a dormant or quiescent phenotype in certain microenvironments both in vivo and in vitro, meaning they can survive as solitary, non-proliferating cells for extended periods before potentially forming metastases.

Research Use: This cell line is crucial for investigating the mechanisms that control the switch from a dormant state to aggressive, proliferative metastatic growth. Researchers use it to study the role of the extracellular matrix (ECM) composition (e.g., type I collagen induces proliferation) and the immune system (e.g., natural killer cells are key for maintaining dormancy) in regulating dormancy.
Dormancy Markers: Dormant D2.0R cells express specific markers such as low levels of the proliferation marker Ki-67, low levels of phosphorylated ERK, high levels of p38, and high levels of dormancy-related genes like Cfh and Gas6.
Culture Conditions: In a standard 3D culture system using a basement membrane extract (BME) matrix, D2.0R cells typically remain quiescent (dormant), while the D2A1 cells proliferate.
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