Canu Giovanni, Correra Rosamaria, Diez-Pinel Guillermo, Castellan Raphaël F P, Denti Laura, Fantin Alessandro, Ruhrberg Christiana
UCL Institute of Ophthalmology, University College London, London EC1V 9EL, UK.
Department of Biosciences, University of Milan, 20133 Milan, Italy.
Development. 2024 Dec 1;151(23). doi: 10.1242/dev.202924. Epub 2024 Dec 4.
During embryonic development, muscle tissues, skin, and a subset of vascular endothelial cells arise from Pax3-expressing embryonic progenitors defined as paraxial mesoderm. By contrast, haemogenic potential is well established for extra-embryonic mesoderm and intra-embryonic lateral plate mesoderm, which do not express Pax3. To date, it is not known whether the haematopoietic system also contains Pax3 lineage cells. Here, we show that the mouse foetal liver and foetal circulation contain a transient population of Pax3 lineage cells with hallmarks of haematopoietic progenitors and the potential to generate both myeloid and erythroid cells. We propose that Pax3 lineage haematopoietic cells should be investigated to better understand normal haematopoietic development from different mesodermal derivatives. Further, genetic alterations of Pax3 lineage haematopoietic cells should be investigated for their potential to cause haematopoietic malignancies.
在胚胎发育过程中,肌肉组织、皮肤以及一部分血管内皮细胞起源于表达Pax3的胚胎祖细胞,这些祖细胞被定义为轴旁中胚层。相比之下,胚外中胚层和胚内侧板中胚层具有明确的造血潜能,它们不表达Pax3。迄今为止,尚不清楚造血系统中是否也含有Pax3谱系细胞。在此,我们表明小鼠胎儿肝脏和胎儿循环中含有一群短暂存在的Pax3谱系细胞,这些细胞具有造血祖细胞的特征,并有产生髓系细胞和红系细胞的潜力。我们建议对Pax3谱系造血细胞进行研究,以更好地理解不同中胚层衍生物的正常造血发育。此外,应研究Pax3谱系造血细胞的基因改变,以了解其导致造血系统恶性肿瘤的可能性。