中文摘要：

盡管我們對(duì)斑馬魚(yú)心臟再生的理解取得了許多進(jìn)展，但研究較少的一個(gè)方面是再生心肌細(xì)胞如何侵入和替代含有膠原蛋白的受傷組織。在這里，我們對(duì)心肌細(xì)胞侵襲的過(guò)程進(jìn)行了深入分析。我們觀察到突出的邊界區(qū)心肌細(xì)胞和巨噬細(xì)胞之間的密切相互作用，并表明巨噬細(xì)胞對(duì)于傷口邊界區(qū)的細(xì)胞外基質(zhì)重塑和心肌細(xì)胞突出到受傷區(qū)域至關(guān)重要。單細(xì)胞 RNA 測(cè)序揭示了編碼膜錨定基質(zhì)金屬蛋白酶的 mmp14b 在邊界區(qū)的幾種細(xì)胞類(lèi)型中的表達(dá)。遺傳性 mmp14b 突變導(dǎo)致巨噬細(xì)胞募集減少、膠原蛋白降解，隨后心肌細(xì)胞突出到受傷組織中。此外，心肌細(xì)胞特異性過(guò)表達(dá) mmp14b 足以增強(qiáng)心肌細(xì)胞侵襲受傷組織和沿傷口頂端表面的滲透。總而言之，我們的數(shù)據(jù)為心臟再生過(guò)程中心肌細(xì)胞侵襲含膠原的受傷組織的機(jī)制提供了重要的見(jiàn)解。

英文摘要：

Despite numerous advances in our understanding of zebrafish cardiac regeneration, an aspect that remains less studied is how regenerating cardiomyocytes invade and replace the collagen-containing injured tissue. Here, we provide an in-depth analysis of the process of cardiomyocyte invasion. We observe close interactions between protruding border-zone cardiomyocytes and macrophages, and show that macrophages are essential for extracellular matrix remodeling at the wound border zone and cardiomyocyte protrusion into the injured area. Single-cell RNA-sequencing reveals the expression of mmp14b, encoding a membrane-anchored matrix metalloproteinase, in several cell types at the border zone. Genetic mmp14b mutation leads to decreased macrophage recruitment, collagen degradation, and subsequent cardiomyocyte protrusion into injured tissue. Furthermore, cardiomyocyte-specific overexpression of mmp14b is sufficient to enhance cardiomyocyte invasion into the injured tissue and along the apical surface of the wound. Altogether, our data provide important insights into the mechanisms underlying cardiomyocyte invasion of the collagen-containing injured tissue during cardiac regeneration.

論文信息：

論文題目：Border-zone cardiomyocytes and macrophages regulate extracellular matrix remodeling to promote cardiomyocyte protrusion during cardiac regeneration

期刊名稱(chēng)：Nature Communications

時(shí)間期卷：16, Article number: 3823 (2025)

在線時(shí)間：2025年4月23日

DOI：doi.org/10.1038/s41467-025-59169-4

產(chǎn)品信息：

貨號(hào)：CP-005-005

規(guī)格：5ml+5ml

品牌：Liposoma

產(chǎn)地：荷蘭

名稱(chēng)：Clodronate Liposomes and Control Liposomes

辦事處：Target Technology（靶點(diǎn)科技）

氯膦酸鹽脂質(zhì)體斑馬魚(yú)巨噬細(xì)胞。斑馬魚(yú)心臟冷凍損傷后，多種細(xì)胞類(lèi)型協(xié)調(diào)對(duì)損傷的反應(yīng)。例如，內(nèi)皮細(xì)胞、心內(nèi)膜細(xì)胞和心外膜細(xì)胞已被證明可提供生長(zhǎng)因子和信號(hào)分子，以促進(jìn)受傷組織的血運(yùn)重建和心肌細(xì)胞再生。成纖維細(xì)胞主要起源于心外膜，已被證明在心臟再生過(guò)程中沉積 ECM 以支持心臟，并且對(duì)損傷后心肌細(xì)胞增殖至關(guān)重要。近年來(lái)，免疫細(xì)胞在促進(jìn)心臟再生過(guò)程中的重要性也得到了認(rèn)可。特別是，巨噬細(xì)胞已被證明在斑馬魚(yú)、蠑螈和新生小鼠心臟的損傷再生中起著重要作用。巨噬細(xì)胞已被證明直接促進(jìn)和調(diào)節(jié)冷凍損傷心臟中瘢痕/ECM 的組成。此外，氯膦酸鹽脂質(zhì)體給藥（荷蘭Liposoma，清除巨噬細(xì)胞）或使用遺傳模型消耗巨噬細(xì)胞會(huì)導(dǎo)致 CM 增殖和再生心臟新生血管形成缺陷。雖然很明顯，許多（如果不是全部）心肌細(xì)胞類(lèi)型在心臟再生過(guò)程中起著至關(guān)重要的作用，但它們對(duì)冷凍損傷后心肌細(xì)胞纖維化組織重新填充的貢獻(xiàn)在很大程度上是未知的。氯膦酸鹽二鈉脂質(zhì)體清除巨噬細(xì)胞在斑馬魚(yú)心臟凍傷模型巨噬細(xì)胞功能研究，荷蘭Liposoma巨噬細(xì)胞清除劑Clodronate Liposomes見(jiàn)刊于Nature Communications：斑馬魚(yú)交界區(qū)心肌細(xì)胞和巨噬細(xì)胞調(diào)節(jié)細(xì)胞外基質(zhì)重塑，促進(jìn)心臟再生過(guò)程中心肌細(xì)胞突出。

Liposoma巨噬細(xì)胞清除劑Clodronate Liposomes氯膦酸二鈉脂質(zhì)體的材料和方法：

Macrophage ablation

Ventricles from Tg(mpeg:NTR-YFP) adult fish were cryoinjured as described above. Cryoinjured fish were then incubated in a 5?μm nifurpirinol or DMSO-control water bath from 4 to 6 days following cryoinjury (replenished daily). Hearts were extracted at 7 dpci and subjected to immunostaining with GFP antibody to check macrophage ablation efficiency and phalloidin staining to quantify CM protrusion at the border zone as described above.

To ablate resident macrophages, Tg(mpeg1:EGFP) adult fish were IP injected with 10?μl clodronate liposomes (5?mg/ml) (Liposoma, Amsterdam, The Netherlands) or PBS 8 days prior to cryoinjury. Hearts were extracted at 7 or 10 dpci followed by cryosection, CHP staining, and phalloidin staining, as described above. Quantification of CHP intensity and CM protrusion at the border zone were performed as described above.

To ablate macrophages at later timepoints, Tg(mpeg1:EGFP) adult fish were IP injected with 10?μl clodronate liposomes (5?mg/ml) (Liposoma, Amsterdam, The Netherlands) or PBS control liposomes at 3, 6, and 9 dpci before collection of hearts at 10 dpci. To study the impact of macrophage ablation on mmp14b overexpression in CMs, Tg(hsp70l:loxP-EGFP-loxP-mmp14b-P2A-tagBFP); Tg(?5.1myl7:CreERT2) adult fish were IP injected with clodronate liposomes or PBS liposomes 1 day prior to cryoinjury and every 4 days afterwards. Tamoxifen/ethanol injections and heat shock were performed to induce mmp14b overexpression as described above. Hearts were extracted at 10 or 21 dpci followed by cryosection and phalloidin or MHC staining as described above. Quantification of CM protrusion at the border zone and CM cortical coverage were performed as described above.