A neuro-lymphatic communication guides lymphatic development by CXCL12/CXCR4 signaling

淋巴系统 生物 淋巴管内皮 淋巴管新生 CXCR4型 细胞生物学 趋化因子受体 PI3K/AKT/mTOR通路 趋化因子 信号转导 蛋白激酶B 免疫学 炎症 遗传学 癌症 转移
作者
Long Nguyen Hoàng,Esteban Delgado,Casey G. Lim,Meriem Bkhache,Amanda Peluzzo,Yi‐Ming Hua,Manisha J. Oza,Sadia Mohsin,Hong Chen,Michael V. Autieri,Seonhee Kim,Xiaolei Liu
出处
期刊:Development [The Company of Biologists]
标识
DOI:10.1242/dev.202901
摘要

Lymphatic vessels grow through active sprouting and mature into a vascular complex including lymphatic capillaries and collecting vessels that ensure fluid transport. However, the signaling cues that direct lymphatic sprouting and patterning remains unclear. In this study, we demonstrated the chemokine signaling, specifically through CXCL12/CXCR4 plays critical roles in regulating lymphatic development. We showed that LEC specific CXCR4 deficient embryos and CXCL12 mutant embryos exhibited server defects in lymphatic sprouting, migration, and lymphatic valve formation. We also discovered that CXCL12, originating from peripheral nerves, directs the migration of dermal lymphatic vessels to align with nerves in developing skin. Deletion CXCR4 or blockage of CXCL12/CXCR4 activity results in reduced VEGFR3 levels on the LEC surface. This, in turn, impairs VEGFC mediated VEGFR3 signaling and downstream PI3K/AKT activities. Taken together, these data identify previously unknown chemokine signaling originating from peripheral nerves that guides dermal lymphatic sprouting and patterning. Our work identifies for the first time a neuro-lymphatics communications during mouse development and reveals a novel mechanism by which CXCR4 modulates VEGFC/VEGFR3/AKT signaling.
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