Polysialic acid blocks mononuclear phagocyte reactivity, inhibits complement activation, and protects from vascular damage in the retina
Medicine (General)
polysialic acid
microglia
Mice, Transgenic
Mice, SCID
QH426-470
Retina
03 medical and health sciences
R5-920
Report
Lectins
Genetics
Animals
Humans
Immunologic Factors
complement
Complement Activation
Phagocytes
0303 health sciences
Lasers
age‐related macular degeneration
Membrane Proteins
Choroidal Neovascularization
3. Good health
Sialic Acids
SIGLEC
DOI:
10.15252/emmm.201606627
Publication Date:
2016-12-22T01:50:48Z
AUTHORS (18)
ABSTRACT
Age-related macular degeneration (AMD) is a major cause of blindness in the elderly population. Its pathophysiology is linked to reactive oxygen species (ROS) and activation of the complement system. Sialic acid polymers prevent ROS production of human mononuclear phagocytes via the inhibitory sialic acid-binding immunoglobulin-like lectin-11 (SIGLEC11) receptor. Here, we show that low-dose intravitreal injection of low molecular weight polysialic acid with average degree of polymerization 20 (polySia avDP20) in humanized transgenic mice expressing SIGLEC11 on mononuclear phagocytes reduced their reactivity and vascular leakage induced by laser coagulation. Furthermore, polySia avDP20 prevented deposition of the membrane attack complex in both SIGLEC11 transgenic and wild-type animals. In vitro, polySia avDP20 showed two independent, but synergistic effects on the innate immune system. First, polySia avDP20 prevented tumor necrosis factor-α, vascular endothelial growth factor A, and superoxide production by SIGLEC11-positive phagocytes. Second, polySia avDP20 directly interfered with complement activation. Our data provide evidence that polySia avDP20 ameliorates laser-induced damage in the retina and thus is a promising candidate to prevent AMD-related inflammation and angiogenesis.
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CITATIONS (73)
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