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Notch 通路调控内皮细胞-周细胞样间充质基质细胞相互作用中血管生成抑制因子激活素 A 的表达。

Notch Pathways Regulate Expression of Angiostatic Factor Activin A in Endothelial-Pericyte-Like Mesenchymal Stromal Cell Interactions.

机构信息

Department of Medicine, College of Medicine, University of Florida, Gainesville, Florida, USA.

Labcorp, Indianapolis, Indiana, USA.

出版信息

Stem Cells Dev. 2023 Jun;32(11-12):301-313. doi: 10.1089/scd.2023.0003. Epub 2023 May 16.

Abstract

Vascularization of ischemic and fabricated tissues is essential for successful tissue repair and replacement therapies. Endothelial cells (ECs) and mesenchymal stem/stromal cells (MSCs) in close proximity spontaneously organize into vessels after coimplantation in semisolid matrices. Thus, local injection of EC mixed with MSC may facilitate tissue (re)vascularization. The organization of these cells into vessels is accompanied by induction of a key regulator of vasculogenesis, activin A, in MSC through juxtacrine pathway. Mechanisms regulating activin A expression are poorly understood; therefore, the contributions of notch signaling pathways were evaluated in EC-adipose mesenchymal stromal cells (ASC) cocultures. Disruption of notch signaling in EC + ASC cocultures with a γ-secretase inhibitor, DAPT, completely abrogated both activin A induction and production, depending on the stage of vasculogenesis. While DAPT stimulated EC proliferation concurrent with increased secretion of vasculogenic factors, it also prevented the crucial transition of ASC from progenitor to smooth muscle cell phenotype, collectively resulting in ineffective tubulogenesis. Silencing Notch2 in ASC abolished activin A production in cocultures, but resulted in normal ASC maturation. In contrast, silencing Notch3 in ASC led to autonomous upregulation of mural cell markers, and intercellular contact with EC further enhanced upregulation of these markers, concurrent with amplified activin A secretion. Strong induction of activin A expression was achieved by exposing ASC to immobilized notch ligand jagged1, whereas jagged1 IgG, added to EC + ASC incubation media, prevented activin A expression. Overall, this study revealed that EC control activin A expression in ASC through juxtacrine notch signaling pathways, and uninterrupted notch signaling is required for activin A production, although signaling through Notch2 and Notch3 produce opposing effects.

摘要

缺血和人工组织的血管化对于成功的组织修复和替代治疗至关重要。内皮细胞(ECs)和间充质干细胞(MSCs)在半固体基质中共同植入后,会自发地在接近的位置组织成血管。因此,局部注射 EC 与 MSC 的混合物可能有助于组织(再)血管化。这些细胞组织成血管的同时,MSC 中诱导了血管生成的关键调节因子激活素 A,通过旁分泌途径。调节激活素 A 表达的机制尚未完全理解;因此,评估了 notch 信号通路在 EC-脂肪间充质基质细胞(ASC)共培养物中的作用。用γ-分泌酶抑制剂 DAPT 破坏 EC+ASC 共培养物中的 notch 信号通路,完全阻断了激活素 A 的诱导和产生,这取决于血管生成的阶段。虽然 DAPT 刺激 EC 增殖,同时增加血管生成因子的分泌,但它也阻止了 ASC 从祖细胞向平滑肌细胞表型的关键转变,共同导致无效的管状生成。在共培养物中沉默 Notch2 可消除 ASC 中的激活素 A 产生,但导致 ASC 正常成熟。相比之下,在 ASC 中沉默 Notch3 导致壁细胞标志物的自主上调,与 EC 的细胞间接触进一步增强了这些标志物的上调,同时激活素 A 的分泌也增强。通过将 ASC 暴露于固定化的 notch 配体 jagged1 来实现激活素 A 表达的强烈诱导,而添加到 EC+ASC 孵育培养基中的 jagged1 IgG 则阻止了激活素 A 的表达。总的来说,这项研究揭示了 EC 通过旁分泌 notch 信号通路控制 ASC 中的激活素 A 表达,并且不间断的 notch 信号对于激活素 A 的产生是必需的,尽管 Notch2 和 Notch3 的信号传递会产生相反的效果。

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