Department of Molecular Biosciences, University of Kansas, Lawrence, Kansas, United States of America.
PLoS One. 2011;6(5):e20180. doi: 10.1371/journal.pone.0020180. Epub 2011 May 23.
The Drosophila egg chamber provides an excellent system in which to study the specification and differentiation of epithelial cell fates because all of the steps, starting with the division of the corresponding stem cells, called follicle stem cells, have been well described and occur many times over in a single ovary.
METHODOLOGY/PRINCIPAL FINDINGS: Here we investigate the role of the small Rab11 GTPase in follicle stem cells (FSCs) and in their differentiating daughters, which include main body epithelial cells, stalk cells and polar cells. We show that rab11-null FSCs maintain their ability to self renew, even though previous studies have shown that FSC self renewal is dependent on maintenance of E-cadherin-based intercellular junctions, which in many cell types, including Drosophila germline stem cells, requires Rab11. We also show that rab11-null FSCs give rise to normal numbers of cells that enter polar, stalk, and epithelial cell differentiation pathways, but that none of the cells complete their differentiation programs and that the epithelial cells undergo premature programmed cell death. Finally we show, through the induction of rab11-null clones at later points in the differentiation program, that Rab11 suppresses tumor-like growth of epithelial cells. Thus, rab11-null epithelial cells arrest differentiation early, assume an aberrant cell morphology, delaminate from the epithelium, and invade the neighboring germline cyst. These phenotypes are associated with defects in E-cadherin localization and a general loss of cell polarity.
CONCLUSIONS/SIGNIFICANCE: While previous studies have revealed tumor suppressor or tumor suppressor-like activity for regulators of endocytosis, our study is the first to identify such activity for regulators of endocytic recycling. Our studies also support the recently emerging view that distinct mechanisms regulate junction stability and plasticity in different tissues.
果蝇卵子发生提供了一个极好的系统,可用于研究上皮细胞命运的特化和分化,因为所有步骤,包括从相应的干细胞——滤泡干细胞开始的分裂,都已被很好地描述,并在单个卵巢中多次发生。
方法/主要发现:在这里,我们研究了小 Rab11 GTPase 在滤泡干细胞(FSCs)及其分化后代中的作用,这些分化后代包括主体上皮细胞、柄细胞和极细胞。我们表明,rab11 缺失的 FSCs 保持其自我更新的能力,尽管之前的研究表明 FSC 的自我更新依赖于维持基于 E-钙粘蛋白的细胞间连接,而在许多细胞类型中,包括果蝇生殖干细胞,这需要 Rab11。我们还表明,rab11 缺失的 FSCs 产生正常数量的细胞进入极性、柄细胞和上皮细胞分化途径,但没有一个细胞完成其分化程序,并且上皮细胞会发生过早的程序性细胞死亡。最后,我们通过在分化程序的后期诱导 rab11 缺失克隆表明,Rab11 抑制上皮细胞的肿瘤样生长。因此,rab11 缺失的上皮细胞早期停止分化,呈现出异常的细胞形态,从上皮层脱离,并侵入邻近的生殖细胞囊中。这些表型与 E-钙粘蛋白定位缺陷和普遍丧失细胞极性有关。
结论/意义:虽然之前的研究已经揭示了内吞作用调节剂的肿瘤抑制因子或肿瘤抑制因子样活性,但我们的研究首次确定了内吞作用回收调节剂的这种活性。我们的研究还支持了最近出现的观点,即不同的机制调节不同组织中连接的稳定性和可塑性。