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IP3 信号对于 Xenopus 胚胎纤毛形成和左右体轴确定是必需的。

IP3 signaling is required for cilia formation and left-right body axis determination in Xenopus embryos.

机构信息

Laboratory for Behavioral and Developmental Disorders, RIKEN Brain Science Institute, Wako-shi, Saitama 351-0198, Japan.

出版信息

Biochem Biophys Res Commun. 2011 Jul 8;410(3):520-4. doi: 10.1016/j.bbrc.2011.06.014. Epub 2011 Jun 7.

Abstract

Vertebrate left-right (LR) body axis is manifested as an asymmetrical alignment of the internal organs such as the heart and the gut. It has been proposed that the process of LR determination commonly involves a cilia-driven leftward flow in the mammalian node and its equivalents (Kupffer's vesicle in zebrafish and the gastrocoel roof plate in Xenopus). Recently, it was reported that Ca(2+) flux regulates Kupffer's vesicle development and is required for LR determination. As a basis of Ca(2+) flux in many cell types, inositol 1,4,5-trisphosphate (IP(3)) receptor-mediated calcium release from the endoplasmic reticulum (ER) plays important roles. However, its involvement in LR determination is poorly understood. We investigated the role of IP(3) signaling in LR determination in Xenopus embryos. Microinjection of an IP(3) receptor-function blocking antibody that can inhibit IP(3) calcium channel activity randomized the LR axis in terms of left-sided Pitx2 expression and organ laterality. In addition, an IP(3) sponge that could inhibit IP(3) signaling by binding IP(3) more strongly than the IP(3) receptor impaired LR determination. Examination of the gastrocoel roof plate revealed that the number of cilia was significantly reduced by IP(3) signal blocking. These results provide evidence that IP(3) signaling is involved in LR asymmetry formation in vertebrates.

摘要

脊椎动物的左右(LR)身体轴表现为内部器官的不对称排列,如心脏和肠道。有人提出,LR 决定的过程通常涉及哺乳动物节点及其等效物(斑马鱼中的 Kupffer 囊泡和非洲爪蟾中的胃腔顶板)中纤毛驱动的向左流动。最近,据报道 Ca(2+) 通量调节 Kupffer 囊泡的发育,并且是 LR 决定所必需的。作为许多细胞类型中 Ca(2+) 通量的基础,三磷酸肌醇(IP(3)) 受体介导的内质网(ER)钙释放在 ER 中发挥重要作用。然而,其在 LR 决定中的作用知之甚少。我们研究了 IP(3) 信号在非洲爪蟾胚胎 LR 决定中的作用。注射可抑制 IP(3) 钙通道活性的 IP(3) 受体功能阻断抗体可使左测 Pitx2 表达和器官偏侧性随机化 LR 轴。此外,通过与 IP(3) 受体相比更强烈地结合 IP(3) 来抑制 IP(3) 信号的 IP(3) 海绵也会损害 LR 决定。对胃腔顶板的检查表明,IP(3) 信号阻断会显著减少纤毛的数量。这些结果表明 IP(3) 信号参与了脊椎动物 LR 不对称形成。

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