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解惑“XXⅩⅩⅩⅩⅩⅩⅩ”-译文小记

中国科研团队构XXⅩⅩⅩⅩⅩⅩⅩ建全球首份多器官衰老时空图谱

来源: 河北日报
2024-11-05 16:10:21

最佳回答

“XXⅩⅩⅩⅩⅩⅩⅩ”中国科研团队构XXⅩⅩⅩⅩⅩⅩⅩ建全球首份多器官衰老时空图谱

  中新XXⅩⅩⅩⅩⅩⅩⅩ社深圳11月5日电 (记者 索XXⅩⅩⅩⅩⅩⅩⅩ有为)中国科学院动物研究所携手华大生命科学研究院、北京基因组研究所(国家生物信息中心),于11月5日在全球顶尖学术期刊《细胞》(Cell)上发表了最新研究成果,该研究利用华大自主研发的“超广角百亿像素生命照相机”——时空组学技术,构建了全球首份多器官衰老时空图谱。

  研究中,研究团队利用时空组学技术Stereo-seq对不同年龄小鼠的心脏、肝脏、脾脏、肺、小肠等9个器官进行了分析,最终形成了一张包含72个细胞类型的多器官衰老时空图谱。这些图谱不仅能“看到”不同细胞内基因的表达情况,还能精确定位每个细胞的位置,如同一部生命衰老的纪录片,展现不同器官在不同年龄段的“模样”。

  通过深入研究,研究团队提出了一个关键指标——“组织结构熵”,可以理解成组织/器官内混乱程度的量化指标。熵越高,器官内部就越混乱,就像一个原本井井有条的房间,随着时间的推移,逐渐变得杂乱无章。研究发现,9个器官中,海马体、脾脏、淋巴结和肝脏熵增最为明显。这意味着这些器官更容易衰老。

  这是首次利用时空组学数据探讨组织熵增,结果表明,结构混乱会导致衰老组织的功能衰退。这对人们了解衰老如何影响组织微环境中的基因表达和细胞相互作用至关重要。

  此外,这项研究还找到一个潜在的延缓衰老的靶点——免疫球蛋白G(IgG)。研究团队发现,IgG会在衰老的“核心区域”(衰老敏感位点)周围大量聚集,就像“煽风点火”一样,加速周围细胞的衰老,特别是诱导巨噬细胞和小胶质细胞进入促衰老状态,从而加剧组织衰老,并且无论在小鼠还是人体的衰老组织中,都观察到了IgG的升高,这表明IgG可能是衰老的一个重要驱动因素。

  研究团队表示,这项研究让人们更深入地了解了衰老的机制,还为科学家提供了延缓衰老的潜在策略——通过精准干预IgG,降低其表达水平,或许就能减缓衰老的进程。(完)

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