Adrenomedullin induces lymphangiogenesis and ameliorates secondary lymphoedema

DH Jin, K Harada, S Ohnishi, K Yamahara… - Cardiovascular …, 2008 - academic.oup.com
DH Jin, K Harada, S Ohnishi, K Yamahara, K Kangawa, N Nagaya
Cardiovascular research, 2008academic.oup.com
Aims Adrenomedullin (AM) is a multifunctional peptide hormone that plays a significant role
in vasodilation and angiogenesis. Lymphoedema is a common but refractory disorder that is
difficult to be treated with conventional therapy. We therefore investigated whether AM
promotes lymphangiogenesis and improves lymphoedema. Methods and results The effects
of AM on lymphatic endothelial cells (LEC) were investigated. AM promoted proliferation,
migration, and network formation of cultured human lymphatic microvascular endothelial …
Aims
Adrenomedullin (AM) is a multifunctional peptide hormone that plays a significant role in vasodilation and angiogenesis. Lymphoedema is a common but refractory disorder that is difficult to be treated with conventional therapy. We therefore investigated whether AM promotes lymphangiogenesis and improves lymphoedema.
Methods and results
The effects of AM on lymphatic endothelial cells (LEC) were investigated. AM promoted proliferation, migration, and network formation of cultured human lymphatic microvascular endothelial cells (HLMVEC). AM increased intracellular cyclic adenosine monophosphate (cAMP) level in HLMVEC. The cell proliferation induced by AM was inhibited by a cAMP antagonist and mitogen-activated protein kinase kinase (MEK) inhibitors. Phosphorylated extracellular signal-regulated kinase (ERK) in HLMVEC was increased by AM. Continuous administration of AM (0.05 µg/kg/min) to BALB/c mice with tail lymphoedema resulted in a decrease in lymphoedema thickness. AM treatment increased the number of lymphatic vessels and blood vessels in the injury site.
Conclusion
AM promoted LEC proliferation at least in part through the cAMP/MEK/ERK pathway, and infusion of AM induced lymphangiogenesis and improved lymphoedema in mice.
Oxford University Press