Geng Xin, Cha Boksik, Mahamud Md Riaj, Lim Kim-Chew, Silasi-Mansat Robert, Uddin Mohammad K M, Miura Naoyuki, Xia Lijun, Simon Alexander M, Engel James Douglas, Chen Hong, Lupu Florea, Srinivasan R Sathish
Cardiovascular Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Department of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI, USA.
Dev Biol. 2016 Jan 1;409(1):218-233. doi: 10.1016/j.ydbio.2015.10.022. Epub 2015 Nov 2.
Lymph is returned to the blood circulation exclusively via four lymphovenous valves (LVVs). Despite their vital importance, the architecture and development of LVVs is poorly understood. We analyzed the formation of LVVs at the molecular and ultrastructural levels during mouse embryogenesis and identified three critical steps. First, LVV-forming endothelial cells (LVV-ECs) differentiate from PROX1(+) progenitors and delaminate from the luminal side of the veins. Second, LVV-ECs aggregate, align perpendicular to the direction of lymph flow and establish lympho-venous connections. Finally, LVVs mature with the recruitment of mural cells. LVV morphogenesis is disrupted in four different mouse models of primary lymphedema and the severity of LVV defects correlate with that of lymphedema. In summary, we have provided the first and the most comprehensive analysis of LVV development. Furthermore, our work suggests that aberrant LVVs contribute to lymphedema.
淋巴液仅通过四个淋巴静脉瓣(LVV)回流至血液循环。尽管它们至关重要,但LVV的结构和发育仍知之甚少。我们在小鼠胚胎发育过程中从分子和超微结构水平分析了LVV的形成,并确定了三个关键步骤。首先,形成LVV的内皮细胞(LVV-EC)从PROX1(+)祖细胞分化而来,并从静脉腔侧脱离。其次,LVV-EC聚集,垂直于淋巴流动方向排列并建立淋巴静脉连接。最后,LVV随着壁细胞的募集而成熟。在四种不同的原发性淋巴水肿小鼠模型中,LVV形态发生受到破坏,LVV缺陷的严重程度与淋巴水肿的严重程度相关。总之,我们提供了对LVV发育的首次也是最全面的分析。此外,我们的研究表明,异常的LVV会导致淋巴水肿。