Genzen Jonathan R, Yang Dan, Ravid Katya, Bordey Angelique
Departments of Neurosurgery & Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, CT 06520-8082, USA.
Cerebrospinal Fluid Res. 2009 Nov 18;6:15. doi: 10.1186/1743-8454-6-15.
Ependymal cells form a protective monolayer between the brain parenchyma and cerebrospinal fluid (CSF). They possess motile cilia important for directing the flow of CSF through the ventricular system. While ciliary beat frequency in airway epithelia has been extensively studied, fewer reports have looked at the mechanisms involved in regulating ciliary beat frequency in ependyma. Prior studies have demonstrated that ependymal cells express at least one purinergic receptor (P2X7). An understanding of the full range of purinergic receptors expressed by ependymal cells, however, is not yet complete. The objective of this study was to identify purinergic receptors which may be involved in regulating ciliary beat frequency in lateral ventricle ependymal cells.
High-speed video analysis of ciliary movement in the presence and absence of purinergic agents was performed using differential interference contrast microscopy in slices of mouse brain (total number of animals = 67). Receptor identification by this pharmacological approach was corroborated by immunocytochemistry, calcium imaging experiments, and the use of two separate lines of knockout mice.
Ciliary beat frequency was enhanced by application of a commonly used P2X7 agonist. Subsequent experiments, however, demonstrated that this enhancement was observed in both P2X7+/+ and P2X7-/- mice and was reduced by pre-incubation with an ecto-5'-nucleotidase inhibitor. This suggested that enhancement was primarily due to a metabolic breakdown product acting on another purinergic receptor subtype. Further studies revealed that ciliary beat frequency enhancement was also induced by adenosine receptor agonists, and pharmacological studies revealed that ciliary beat frequency enhancement was primarily due to A2B receptor activation. A2B expression by ependymal cells was subsequently confirmed using A2B-/-/beta-galactosidase reporter gene knock-in mice.
This study demonstrates that A2B receptor activation enhances ciliary beat frequency in lateral ventricle ependymal cells. Ependymal cell ciliary beat frequency regulation may play an important role in cerebral fluid balance and cerebrospinal fluid dynamics.
室管膜细胞在脑实质和脑脊液(CSF)之间形成一层保护性单层结构。它们具有可运动的纤毛,对引导脑脊液通过脑室系统的流动至关重要。虽然气道上皮细胞的纤毛摆动频率已得到广泛研究,但关于调节室管膜细胞纤毛摆动频率的机制的报道较少。先前的研究表明,室管膜细胞表达至少一种嘌呤能受体(P2X7)。然而,对室管膜细胞表达的所有嘌呤能受体的全面了解尚未完成。本研究的目的是鉴定可能参与调节侧脑室室管膜细胞纤毛摆动频率的嘌呤能受体。
使用微分干涉对比显微镜对小鼠脑切片中存在和不存在嘌呤能试剂时的纤毛运动进行高速视频分析(动物总数 = 67)。通过免疫细胞化学、钙成像实验以及使用两种不同品系的基因敲除小鼠,对这种药理学方法进行的受体鉴定进行了验证。
应用常用的P2X7激动剂可提高纤毛摆动频率。然而,随后的实验表明,在P2X7+/+和P2X7-/-小鼠中均观察到这种提高,并且用外切5'-核苷酸酶抑制剂预孵育可使其降低。这表明这种提高主要是由于一种代谢分解产物作用于另一种嘌呤能受体亚型。进一步的研究表明,腺苷受体激动剂也可诱导纤毛摆动频率提高,并且药理学研究表明,纤毛摆动频率提高主要是由于A2B受体激活。随后使用A2B-/-/β-半乳糖苷酶报告基因敲入小鼠证实了室管膜细胞中A2B的表达。
本研究表明,A2B受体激活可提高侧脑室室管膜细胞的纤毛摆动频率。室管膜细胞纤毛摆动频率的调节可能在脑液平衡和脑脊液动力学中起重要作用。