Suppr超能文献

系膜生成祖细胞:造血的一个中胚层生成和血管生成分支?一个被忽视的可塑性故事。

Mesangiogenic progenitor cells: a mesengenic and vasculogenic branch of hemopoiesis? A story of neglected plasticity.

作者信息

Pacini Simone

机构信息

Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

出版信息

Front Cell Dev Biol. 2025 Mar 24;13:1513440. doi: 10.3389/fcell.2025.1513440. eCollection 2025.

Abstract

Mesangiogenic progenitor cells (MPCs) are mesengenic and vasculogenic cells isolated from human bone marrow mononuclear cell cultures. Although MPCs were first described over two decades ago and have demonstrated promising differentiation capabilities, these cells did not attract sufficient attention from experts in the field of tissue regeneration. Several reports from the first decade of the 2000s showed MPC-like cells co-isolated in primary mesenchymal stromal cell (MSC) cultures, applying human serum. However, in most cases, these rounded and firmly attached cells were described as "contaminating" cells of hemopoietic origin. Indeed, MPC morphology, phenotype, and functional features evoke but do not completely overlap with those of cultured peripheral macrophages, and their hemopoietic origin should not be excluded. The plasticity of cells from the monocyte lineage is surprising but not completely unprecedented. Underestimated data demonstrated that circulating monocyte/macrophages could acquire broader plasticity under specific and different culture conditions, and this plasticity could be a consequence of de-differentiation. The evidence discussed here suggests that MPCs could represent the cell identity toward which the de-differentiation process reprograms the circulating mature phagocytic compartment.

摘要

肾小球生成祖细胞(MPCs)是从人骨髓单个核细胞培养物中分离出来的成血管细胞和血管生成细胞。尽管MPCs在二十多年前就首次被描述,并且已经展示出了有前景的分化能力,但这些细胞并未引起组织再生领域专家的足够关注。21世纪第一个十年的几份报告显示,在应用人血清的原代间充质基质细胞(MSC)培养物中共同分离出了MPC样细胞。然而,在大多数情况下,这些圆形且牢固附着的细胞被描述为造血来源的“污染”细胞。实际上,MPC的形态、表型和功能特征与培养的外周巨噬细胞的特征相似但并不完全重叠,并且它们的造血起源也不应被排除。单核细胞谱系细胞的可塑性令人惊讶,但并非完全史无前例。未得到充分重视的数据表明,循环单核细胞/巨噬细胞在特定且不同的培养条件下可以获得更广泛的可塑性,而这种可塑性可能是去分化的结果。这里讨论的证据表明,MPCs可能代表了去分化过程将循环成熟吞噬细胞区室重新编程所趋向的细胞身份。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5297/11973335/1e82e5f9d11b/fcell-13-1513440-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验