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新型自组装肽水凝胶脑内给药安全,并支持实验性脑出血中的细胞增殖。

Intracerebral Administration of a Novel Self-Assembling Peptide Hydrogel Is Safe and Supports Cell Proliferation in Experimental Intracerebral Haemorrhage.

机构信息

Geoffrey Jefferson Brain Research Centre, Manchester Academic Health Science Centre, Northern Care Alliance NHS Foundation Trust, The University of Manchester, Manchester, M13 9PT, UK.

Division of Neuroscience, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, M13 9PT, UK.

出版信息

Transl Stroke Res. 2024 Oct;15(5):986-1004. doi: 10.1007/s12975-023-01189-7. Epub 2023 Oct 18.

DOI:10.1007/s12975-023-01189-7
PMID:37853252
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11364698/
Abstract

Intracerebral haemorrhage (ICH) is the deadliest form of stroke, but current treatment options are limited, meaning ICH survivors are often left with life-changing disabilities. The significant unmet clinical need and socioeconomic burden of ICH mean novel regenerative medicine approaches are gaining interest. To facilitate the regeneration of the ICH lesion, injectable biomimetic hydrogels are proposed as both scaffolds for endogenous repair and delivery platforms for pro-regenerative therapies. In this paper, the objective was to explore whether injection of a novel self-assembling peptide hydrogel (SAPH) Alpha2 was feasible, safe and could stimulate brain tissue regeneration, in a collagenase-induced ICH model in rats. Alpha2 was administered intracerebrally at 7 days post ICH and functional outcome measures, histological markers of damage and repair and RNA-sequencing were investigated for up to 8 weeks. The hydrogel Alpha2 was safe, well-tolerated and was retained in the lesion for several weeks, where it allowed infiltration of host cells. The hydrogel had a largely neutral effect on functional outcomes and expression of angiogenic and neurogenic markers but led to increased numbers of proliferating cells. RNAseq and pathway analysis showed that ICH altered genes related to inflammatory and phagocytic pathways, and these changes were also observed after administration of hydrogel. Overall, the results show that the novel hydrogel was safe when injected intracerebrally and had no negative effects on functional outcomes but increased cell proliferation. To elicit a regenerative effect, future studies could use a functionalised hydrogel or combine it with an adjunct therapy.

摘要

脑出血 (ICH) 是中风中最致命的一种,但目前的治疗选择有限,这意味着 ICH 幸存者往往会留下改变生活的残疾。ICH 显著的未满足的临床需求和社会经济负担意味着新的再生医学方法越来越受到关注。为了促进 ICH 病变的再生,可注射仿生水凝胶被提议作为内源性修复的支架和促进再生疗法的递药平台。在本文中,目的是探索在胶原酶诱导的大鼠 ICH 模型中,注射新型自组装肽水凝胶 (SAPH) Alpha2 是否可行、安全且能刺激脑组织再生。在 ICH 后 7 天,将 Alpha2 脑内注射,并在长达 8 周的时间内进行功能结局测量、损伤和修复的组织学标志物以及 RNA 测序研究。水凝胶 Alpha2 安全、耐受良好,可在病变部位保留数周,允许宿主细胞浸润。该水凝胶对功能结局和血管生成及神经生成标志物的表达基本没有影响,但导致增殖细胞数量增加。RNAseq 和通路分析表明,ICH 改变了与炎症和吞噬途径相关的基因,在给予水凝胶后也观察到这些变化。总体而言,结果表明,新型水凝胶脑内注射是安全的,对功能结局没有负面影响,但能增加细胞增殖。为了产生再生效果,未来的研究可以使用功能化水凝胶或将其与辅助治疗结合使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a161/11364698/c0aed4d9c368/12975_2023_1189_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a161/11364698/fc6d9a6ae90c/12975_2023_1189_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a161/11364698/ef23d7c40979/12975_2023_1189_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a161/11364698/610d5dc7760d/12975_2023_1189_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a161/11364698/f8eb61e492f3/12975_2023_1189_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a161/11364698/4ddf729b658f/12975_2023_1189_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a161/11364698/6e1a09d85ce9/12975_2023_1189_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a161/11364698/b2b312333d5c/12975_2023_1189_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a161/11364698/76910687e4af/12975_2023_1189_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a161/11364698/c0aed4d9c368/12975_2023_1189_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a161/11364698/fc6d9a6ae90c/12975_2023_1189_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a161/11364698/ef23d7c40979/12975_2023_1189_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a161/11364698/610d5dc7760d/12975_2023_1189_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a161/11364698/f8eb61e492f3/12975_2023_1189_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a161/11364698/4ddf729b658f/12975_2023_1189_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a161/11364698/6e1a09d85ce9/12975_2023_1189_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a161/11364698/b2b312333d5c/12975_2023_1189_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a161/11364698/76910687e4af/12975_2023_1189_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a161/11364698/c0aed4d9c368/12975_2023_1189_Fig9_HTML.jpg

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