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表皮生长因子样结构域 7 通过整合素 αvβ3 驱动脑淋巴内皮细胞的发育。

Epidermal growth factor-like domain 7 drives brain lymphatic endothelial cell development through integrin αvβ3.

机构信息

School of Life Sciences, Department of Anaesthesia of Zhongshan Hospital, Fudan University, 200438, Shanghai, China.

Institute of Developmental Biology and Regenerative Medicine, Southwest University, 400715, Chongqing, China.

出版信息

Nat Commun. 2024 Jul 16;15(1):5986. doi: 10.1038/s41467-024-50389-8.

Abstract

In zebrafish, brain lymphatic endothelial cells (BLECs) are essential for meningeal angiogenesis and cerebrovascular regeneration. Although epidermal growth factor-like domain 7 (Egfl7) has been reported to act as a pro-angiogenic factor, its roles in lymphangiogenesis remain unclear. Here, we show that Egfl7 is expressed in both blood and lymphatic endothelial cells. We generate an egfl7 mutant with a 13-bp-deletion in exon 3 leading to reduced expression of Egfl7. The egfl7 mutant zebrafish exhibit defective formation of BLEC bilateral loop-like structures, although trunk and facial lymphatic development remains unaffected. Moreover, while the egfl7 mutant displays normal BLEC lineage specification, the migration and proliferation of these cells are impaired. Additionally, we identify integrin αvβ3 as the receptor for Egfl7. αvβ3 is expressed in the CVP and sprouting BLECs, and blocking this integrin inhibits the formation of BLEC bilateral loop-like structures. Thus, this study identifies a role for Egfl7 in BLEC development that is mediated through the integrin αvβ3.

摘要

在斑马鱼中,脑淋巴内皮细胞(BLEC)对于脑脊膜血管生成和脑血管再生至关重要。尽管表皮生长因子样结构域 7(Egfl7)已被报道作为一种促血管生成因子,但它在淋巴管生成中的作用尚不清楚。在这里,我们表明 Egfl7 在血液和淋巴内皮细胞中均有表达。我们生成了一个 Egfl7 突变体,该突变体在第 3 外显子中缺失了 13 个碱基,导致 Egfl7 的表达减少。Egfl7 突变体斑马鱼表现出 BLEC 双侧环样结构形成缺陷,尽管躯干和面部淋巴管发育仍未受影响。此外,虽然 egfl7 突变体显示出正常的 BLEC 谱系特化,但这些细胞的迁移和增殖受到损害。此外,我们鉴定出整合素αvβ3 是 Egfl7 的受体。αvβ3 在 CVP 和出芽 BLEC 中表达,阻断该整合素抑制 BLEC 双侧环样结构的形成。因此,这项研究确定了 Egfl7 在 BLEC 发育中的作用,该作用是通过整合素αvβ3 介导的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62bb/11252342/d0782d906a37/41467_2024_50389_Fig1_HTML.jpg

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