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生物刺激填充剂与炎症通路的诱导:对巨噬细胞对羟磷灰石钙和聚左旋乳酸反应的临床前研究。

Biostimulating fillers and induction of inflammatory pathways: A preclinical investigation of macrophage response to calcium hydroxylapatite and poly-L lactic acid.

机构信息

R&D, Merz Aesthetics GmbH, Frankfurt am Main, Germany.

Private Practice, Geelong, Victoria, Australia.

出版信息

J Cosmet Dermatol. 2024 Jan;23(1):99-106. doi: 10.1111/jocd.15928. Epub 2023 Aug 18.

DOI:10.1111/jocd.15928
PMID:37593832
Abstract

INTRODUCTION

Initial macrophage response to biostimulatory substances is key in determining the subsequent behavior of fibroblasts and the organization of newly synthesized collagen. Though histological studies suggest that calcium hydroxylapatite (CaHA) filler initiates a regenerative healing response with collagen and elastin deposition similar to natural, healthy tissue rather than an inflammatory response with fibrosis, the relative activity of macrophages stimulated by CaHA, as well as how this activity compares to that induced by other biostimulatory fillers, has not been explored. The aim of the study is to characterize the in vitro macrophage response to two biostimulory fillers, CaHA and PLLA (poly-L lactic acid), and to evaluate their inflammatory potential.

METHODS

Primary human macrophages were incubated with two dilutions (1:50 and 1:100) of commercially available CaHA or PLLA. After 24 h incubation, an inflammation array was used to screen for the expression of 40 cytokines, released by macrophages. ELISA was used to confirm array results.

RESULTS

Four cytokines were significantly upregulated in M1 macrophages incubated with PLLA compared to both unstimulated controls and CaHA: CCL1 (p < 0.001), TNFRII (p < 0.01), MIP-1α (p < 0.05), and IL-8 (p < 0.001). In M2 macrophages, MIP-1α (p < 0.01) and MIP-1β (p < 0.01) were significantly upregulated by PLLA compared to CaHA and unstimulated controls.

CONCLUSION

Together, these findings indicate that the CaHA mode of action is a non-inflammatory response while PLLA initiates expression of several cytokines known to play a role in inflammation. Our study supports the concept that these two "biostimulatory" fillers follow distinct pathways and should be considered individually with regard to mechanism of action.

摘要

简介

初始巨噬细胞对生物刺激物质的反应是决定成纤维细胞后续行为和新合成胶原组织的关键。尽管组织学研究表明,钙羟基磷灰石(CaHA)填充剂引发的再生愈合反应伴随着胶原蛋白和弹性蛋白的沉积,类似于天然、健康的组织,而不是纤维化的炎症反应,但 CaHA 刺激的巨噬细胞的相对活性,以及这种活性与其他生物刺激填充剂诱导的活性相比,尚未得到探索。本研究旨在表征两种生物刺激填充剂(CaHA 和 PLLA)对原代人巨噬细胞的体外反应,并评估其炎症潜能。

方法

将两种商业上可获得的 CaHA 或 PLLA 稀释液(1:50 和 1:100)与原代人巨噬细胞孵育。孵育 24 小时后,用炎症芯片筛选巨噬细胞释放的 40 种细胞因子的表达。采用 ELISA 法对芯片结果进行确认。

结果

与未刺激对照和 CaHA 相比,PLLA 孵育的 M1 巨噬细胞中有 4 种细胞因子明显上调:CCL1(p<0.001)、TNFRII(p<0.01)、MIP-1α(p<0.05)和 IL-8(p<0.001)。在 M2 巨噬细胞中,与 CaHA 和未刺激对照相比,MIP-1α(p<0.01)和 MIP-1β(p<0.01)被 PLLA 显著上调。

结论

综上所述,这些发现表明 CaHA 的作用模式是非炎症反应,而 PLLA 则引发了几种已知在炎症中发挥作用的细胞因子的表达。我们的研究支持这样一种概念,即这两种“生物刺激”填充剂遵循不同的途径,应单独考虑其作用机制。

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