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栀子苷通过激活 STAT6-PPAR-γ 通路指导和维持巨噬细胞向促再生的 M2 亚型极化。

Genipin guides and sustains the polarization of macrophages to the pro-regenerative M2 subtype via activation of the pSTAT6-PPAR-gamma pathway.

机构信息

Department of Urology, University Hospitals Cleveland Medical Center, Case Western Reserve University, Cleveland, OH 44106, USA.

Department of Mechanical and Aerospace Engineering, Case Western Reserve University, Cleveland, OH 44106, USA.

出版信息

Acta Biomater. 2021 Sep 1;131:198-210. doi: 10.1016/j.actbio.2021.06.043. Epub 2021 Jul 2.

Abstract

M2 macrophages are associated with deposition of interstitial collagen and other extracellular matrix proteins during the course wound healing and also inflammatory response to biomaterials. Developing advanced biomaterials to promote the M2 subtype may be an effective way to improve tissue reinforcement surgery outcomes. In this study, the effect of genipin, a naturally derived crosslinking agent, on M0 → M2-polarization was investigated. Genipin was introduced either indirectly by seeding cells on aligned collagen biotextiles that are crosslinked by the agent or in soluble form by direct addition to the culture medium. Cellular elongation effects on macrophage polarization induced by the collagen biotextile were also investigated as a potential inducer of macrophage polarization. M0 and M2 macrophages demonstrated significant elongation on the surface of aligned collagen threads, while cells of the M1 subtype-maintained a round phenotype. M0 → M2 polarization, as reflected by arginase and Ym-1 production, was observed on collagen threads only when the threads were crosslinked by genipin, implicating genipin as a more potent inducer of the regenerative phenotype compared to cytoskeletal elongation. The addition of genipin to the culture medium directly also drove the emergence of pro-regenerative phenotype as measured by the markers (arginase and Ym-1) and through the activation of the pSTAT6-PPAR-gamma pathway. This study indicates that genipin-crosslinked collagen biotextiles can be used as a delivery platform to promote regenerative response after biomaterial implantation. STATEMENT OF SIGNIFICANCE: The immune response is one of the key determinants of tissue repair and regeneration rate, and outcome. The M2 macrophage subtype is known to resolve the inflammatory response and support tissue repair by producing pro-regenerative factors. Therefore, a biomaterial that promotes M2 sub-type can be a viable strategy to enhance tissue regeneration. In this study, we investigated genipin-crosslinked electrochemically aligned collagen biotextiles for their capacity to induce pro-regenerative polarization of M0 macrophages. The results demonstrated that genipin, rather than matrix-induced cellular elongation, was responsible for M0 → M2 polarization in the absence of other bioinductive factors and maintaining the M2 polarized status of macrophages. Furthermore, we identified that genipin polarizes the M2 macrophage phenotype via activation of the pSTAT6-PPAR-gamma pathway.

摘要

M2 巨噬细胞与间质胶原和其他细胞外基质蛋白的沉积有关,在伤口愈合过程中也与生物材料的炎症反应有关。开发促进 M2 亚型的先进生物材料可能是改善组织增强手术效果的有效方法。在这项研究中,研究了天然交联剂京尼平对 M0→M2 极化的影响。通过将细胞接种在通过该试剂交联的定向胶原生物纺织品上或通过直接添加到培养基中,间接地引入京尼平。还研究了胶原生物纺织品对巨噬细胞极化诱导的细胞伸长效应作为巨噬细胞极化的潜在诱导剂。M0 和 M2 巨噬细胞在定向胶原纤维表面显示出明显的伸长,而 M1 亚型的细胞保持圆形表型。只有当纤维被京尼平交联时,才会在胶原纤维上观察到 M0→M2 极化,表现为精氨酸酶和 Ym-1 的产生,这表明京尼平比细胞骨架伸长更能诱导再生表型。直接向培养基中添加京尼平也通过标记物(精氨酸酶和 Ym-1)和通过激活 pSTAT6-PPAR-γ途径来驱动再生表型的出现。这项研究表明,京尼平交联的胶原生物纺织品可用作递送平台,以促进生物材料植入后的再生反应。 意义声明:免疫反应是组织修复和再生率以及结果的关键决定因素之一。已知 M2 巨噬细胞亚型通过产生促再生因子来解决炎症反应并支持组织修复。因此,促进 M2 亚群的生物材料可以是增强组织再生的可行策略。在这项研究中,我们研究了京尼平交联的电化学定向胶原生物纺织品在诱导 M0 巨噬细胞产生促再生极化方面的能力。结果表明,在没有其他生物诱导因子的情况下,京尼平而不是基质诱导的细胞伸长负责 M0→M2 极化,并维持巨噬细胞的 M2 极化状态。此外,我们确定京尼平通过激活 pSTAT6-PPAR-γ途径来极化 M2 巨噬细胞表型。

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本文引用的文献

1
Macrophage Polarization in Response to Collagen Scaffold Stiffness Is Dependent on Cross-Linking Agent Used To Modulate the Stiffness.
ACS Biomater Sci Eng. 2019 Feb 11;5(2):544-552. doi: 10.1021/acsbiomaterials.8b00910. Epub 2018 Dec 17.
2
The Use of Genipin as an Effective, Biocompatible, Anti-Inflammatory Cross-Linking Method for Nerve Guidance Conduits.
Adv Biosyst. 2020 Mar;4(3):e1900212. doi: 10.1002/adbi.201900212. Epub 2020 Feb 6.
3
Collagen Fibril Density Modulates Macrophage Activation and Cellular Functions during Tissue Repair.
Bioengineering (Basel). 2020 Mar 31;7(2):33. doi: 10.3390/bioengineering7020033.
5
Genetic programming of macrophages to perform anti-tumor functions using targeted mRNA nanocarriers.
Nat Commun. 2019 Sep 3;10(1):3974. doi: 10.1038/s41467-019-11911-5.
6
Gene expression in stress urinary incontinence: a systematic review.
Int Urogynecol J. 2020 Jan;31(1):1-14. doi: 10.1007/s00192-019-04025-5. Epub 2019 Jul 16.
7
Transcriptome profile of rat genes in bone marrow-derived macrophages at different activation statuses by RNA-sequencing.
Genomics. 2019 Jul;111(4):986-996. doi: 10.1016/j.ygeno.2018.06.006. Epub 2018 Jul 6.
9
Biomaterials: Foreign Bodies or Tuners for the Immune Response?
Int J Mol Sci. 2019 Feb 1;20(3):636. doi: 10.3390/ijms20030636.
10
Woven collagen biotextiles enable mechanically functional rotator cuff tendon regeneration during repair of segmental tendon defects in vivo.
J Biomed Mater Res B Appl Biomater. 2019 Aug;107(6):1864-1876. doi: 10.1002/jbm.b.34279. Epub 2018 Nov 28.

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