Plexin D1 negatively regulates zebrafish lymphatic development

被引:2
|
作者
Britto, Denver D. [1 ]
He, Jia [2 ]
Misa, June P. [1 ]
Chen, Wenxuan [1 ]
Kakadia, Purvi M. [1 ,3 ]
Grimm, Lin [4 ,5 ,6 ]
Herbert, Caitlin D. [1 ]
Crosier, Kathryn E. [1 ]
Crosier, Philip S. [1 ]
Bohlander, Stefan K. [1 ,3 ]
Hogan, Benjamin M. [4 ,5 ,6 ]
Hall, Christopher J. [1 ]
Torres-Vazquez, Jesus [2 ]
Astin, Jonathan W. [1 ]
机构
[1] Univ Auckland, Sch Med Sci, Dept Mol Med & Pathol, Auckland 1023, New Zealand
[2] NYU, Skirball Inst Biomol Med, Grossman Sch Med, New York, NY 10016 USA
[3] Univ Auckland, Fac Med & Hlth Sci, Dept Mol Med & Pathol, Leukaemia & Blood Canc Res Unit, Auckland 1023, New Zealand
[4] Peter MacCallum Canc Ctr, Organogenesis & Canc Program, Melbourne, Vic 3000, Australia
[5] Univ Melbourne, Sir Peter MacCallum Dept Oncol, Melbourne, Vic 3010, Australia
[6] Univ Melbourne, Dept Anat & Physiol, Melbourne, Vic 3010, Australia
来源
DEVELOPMENT | 2022年 / 149卷 / 21期
基金
美国国家卫生研究院;
关键词
Plexin D1; Lymphatic; Zebrafish; Lymphangiogenesis; VEGFR; ENDOTHELIAL-CELLS; SEMAPHORIN; 3E-PLEXIN-D1; NETWORK FORMATION; VEGF-C; LYMPHANGIOGENESIS; ANGIOGENESIS; VESSELS; EXPRESSION; ERK; ACTIVATION;
D O I
10.1242/dev.200560
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Lymphangiogenesis is a dynamic process that involves the directed migration of lymphatic endothelial cells (LECs) to form lymphatic vessels. The molecular mechanisms that underpin lymphatic vessel patterning are not fully elucidated and, to date, no global regulator of lymphatic vessel guidance is known. In this study, we identify the transmembrane cell signalling receptor Plexin D1 (Plxnd1) as a negative regulator of both lymphatic vessel guidance and lymphangiogenesis in zebrafish. plxnd1 is expressed in developing lymphatics and is required for the guidance of both the trunk and facial lymphatic networks. Loss of plxnd1 is associated with misguided intersegmental lymphatic vessel growth and aberrant facial lymphatic branches. Lymphatic guidance in the trunk is mediated, at least in part, by the Plxnd1 ligands, Semaphorin 3AA and Semaphorin 3C. Finally, we show that Plxnd1 normally antagonises Vegfr/Erk signalling to ensure the correct number of facial LECs and that loss of plxnd1 results in facial lymphatic hyperplasia. As a global negative regulator of lymphatic vessel development, the Sema/Plxnd1 signalling pathway is a potential therapeutic target for treating diseases associated with dysregulated lymphatic growth.
引用
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页数:14
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