心脏发育过程中心脏内皮细胞的细胞间遗传示踪。
Intercellular genetic tracing of cardiac endothelium in the developing heart.
机构信息
Key Laboratory of Systems Health Science of Zhejiang Province, School of Life Science, Hangzhou Institute for Advanced Study, University of Chinese Academy of Sciences, Hangzhou 310024, China; New Cornerstone Science Laboratory, State Key Laboratory of Cell Biology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, University of Chinese Academy of Sciences, Shanghai 200031, China.
New Cornerstone Science Laboratory, State Key Laboratory of Cell Biology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, University of Chinese Academy of Sciences, Shanghai 200031, China.
出版信息
Dev Cell. 2023 Aug 21;58(16):1502-1512.e3. doi: 10.1016/j.devcel.2023.05.021. Epub 2023 Jun 21.
Cardiac resident macrophages play vital roles in heart development, homeostasis, repair, and regeneration. Recent studies documented the hematopoietic potential of cardiac endothelium that supports the generation of cardiac macrophages and peripheral blood cells in mice. However, the conclusion was not strongly supported by previous genetic tracing studies, given the non-specific nature of conventional Cre-loxP tracing tools. Here, we develop an intercellular genetic labeling system that can permanently trace heart-specific endothelial cells based on cell-cell interaction in mice. Results from cell-cell contact-mediated genetic fate mapping demonstrate that cardiac endothelial cells do not exhibit hemogenic potential and do not contribute to cardiac macrophages or other circulating blood cells. This Matters Arising paper is in response to Shigeta et al. (2019), published in Developmental Cell. See also the response by Liu and Nakano (2023), published in this issue.
心肌驻留巨噬细胞在心脏发育、稳态、修复和再生中发挥着重要作用。最近的研究记录了心脏内皮细胞的造血潜能,该潜能支持了小鼠心肌巨噬细胞和外周血细胞的生成。然而,由于传统的 Cre-loxP 示踪工具的非特异性,这一结论并没有得到先前遗传示踪研究的有力支持。在这里,我们开发了一种细胞间遗传标记系统,可以基于细胞-细胞相互作用在小鼠体内永久追踪心脏特异性内皮细胞。基于细胞接触介导的遗传命运图谱的结果表明,心脏内皮细胞没有表现出造血潜能,也不会产生心肌巨噬细胞或其他循环血细胞。这篇来稿是对 Shigeta 等人(2019)在《发育细胞》上发表的论文的回应。也可参见 Liu 和 Nakano(2023)在本期杂志上发表的回应。