Currle D Spencer, Cheng Xun, Hsu Ching-Mei, Monuki Edwin S
Department of Pathology, University of California, Irvine, D440 Medical Sciences I, Irvine, CA 92697-4800, USA.
Development. 2005 Aug;132(15):3549-59. doi: 10.1242/dev.01915. Epub 2005 Jun 23.
Choroid plexus (CP) produces the cerebrospinal fluid (CSF) of the central nervous system (CNS), but little is known about the mechanisms underlying development of this important tissue. CP forms in the hindbrain (4th ventricle), diencephalon (3rd ventricle) and dorsomedial telencephalon bilaterally (lateral ventricles). All of these sites lie at or near the embryonic dorsal midline (DM), which acts as a CNS patterning center. We therefore examined DM-CP relationships using normal and Gdf7 (Bmp12) transgenic embryos to fate map or ablate DM cells. These studies revealed a Gdf7 fate map that includes most CP epithelial (CPe) cells of the hindbrain and diencephalon. In the telencephalon, Gdf7 cell lineages were found in the small anterior domain of telencephalic CPe (tCPe), but its large posterior domain was devoid of these lineages. Anterior and posterior tCPe domains, which arise within a contiguous field separate from diencephalic CPe, also exhibited different patterns of apoptosis. Despite lacking Gdf7 cell lineages, the posterior tCPe domain failed to form after ablating Gdf7-expressing DM cells at neural tube stages. The tCPe loss was associated with abrogation of high-level bone morphogenetic protein (Bmp) signaling, which is known to be required for tCPe induction. Taken together, these studies demonstrate intimate DM-CPe relationships throughout the CNS and highlight two distinct tCPe domains, including a posterior domain whose genesis depends on DM cells in a non-cell-autonomous fashion.
脉络丛(CP)产生中枢神经系统(CNS)的脑脊液(CSF),但对于这个重要组织发育的潜在机制知之甚少。CP在双侧后脑(第四脑室)、间脑(第三脑室)和端脑背内侧(侧脑室)形成。所有这些部位都位于胚胎背中线(DM)处或其附近,而背中线起着中枢神经系统模式形成中心的作用。因此,我们使用正常和Gdf7(Bmp12)转基因胚胎来追踪命运或消融DM细胞,以研究DM与CP的关系。这些研究揭示了一个Gdf7命运图谱,其中包括后脑和间脑的大多数CP上皮(CPe)细胞。在端脑中,在端脑CPe(tCPe)的小前区发现了Gdf7细胞谱系,但其大后区没有这些谱系。与间脑CPe分开的连续区域内出现的前、后tCPe区域也表现出不同的凋亡模式。尽管缺乏Gdf7细胞谱系,但在神经管阶段消融表达Gdf7的DM细胞后,后tCPe区域未能形成。tCPe的缺失与高水平骨形态发生蛋白(Bmp)信号的消除有关,已知Bmp信号是诱导tCPe所必需的。综上所述,这些研究证明了整个中枢神经系统中DM与CPe之间密切的关系,并突出了两个不同的tCPe区域,包括一个后区,其发生以非细胞自主方式依赖于DM细胞。