ganglioside gt1b
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2020 ◽  
Vol 27 (1) ◽  
pp. 278-289
Author(s):  
Jin-Woo Kim ◽  
Hyo-Jin Park ◽  
Seul-Gi Yang ◽  
Min-Ji Kim ◽  
In-Su Kim ◽  
...  

2019 ◽  
Vol 21 (1) ◽  
pp. 106 ◽  
Author(s):  
Bo Hyun Kim ◽  
Won Seok Ju ◽  
Ji-Su Kim ◽  
Sun-Uk Kim ◽  
Soon Ju Park ◽  
...  

Gangliosides are sialic acid-containing glycosphingolipids, which are the most abundant family of glycolipids in eukaryotes. Gangliosides have been suggested to be important lipid molecules required for the control of cellular procedures, such as cell differentiation, proliferation, and signaling. GD1a is expressed in interstitial cells during ovarian maturation in mice and exogenous GD1a is important to oocyte maturation, monospermic fertilization, and embryonic development. In this context, GM1 is known to influence signaling pathways in cells and is important in sperm–oocyte interactions and sperm maturation processes, such as capacitation. GM3 is expressed in the vertebrate oocyte cytoplasm, and exogenously added GM3 induces apoptosis and DNA injury during in vitro oocyte maturation and embryogenesis. As a consequence of this, ganglioside GT1b and GM1 decrease DNA fragmentation and act as H2O2 inhibitors on germ cells and preimplantation embryos. This review describes the functional roles of gangliosides in spermatozoa, oocytes, and early embryonic development.


2015 ◽  
Vol 61 (6) ◽  
pp. 549-557 ◽  
Author(s):  
Seon-Ung HWANG ◽  
Yubyeol JEON ◽  
Junchul David YOON ◽  
Lian CAI ◽  
Eunhye KIM ◽  
...  

2012 ◽  
Vol 517 (2) ◽  
pp. 140-143 ◽  
Author(s):  
Shun Watanabe ◽  
Hideyoshi Higashi ◽  
Hideoki Ogawa ◽  
Kenji Takamori ◽  
Kazuhisa Iwabuchi

2009 ◽  
Vol 83 (19) ◽  
pp. 10275-10279 ◽  
Author(s):  
Kimberly D. Erickson ◽  
Robert L. Garcea ◽  
Billy Tsai

ABSTRACT The Merkel cell polyomavirus (MCPyV) was identified recently in human Merkel cell carcinomas, an aggressive neuroendocrine skin cancer. Here, we identify a putative host cell receptor for MCPyV. We found that recombinant MCPyV VP1 pentameric capsomeres both hemagglutinated sheep red blood cells and interacted with ganglioside GT1b in a sucrose gradient flotation assay. Structural differences between the analyzed gangliosides suggest that MCPyV VP1 likely interacts with sialic acids on both branches of the GT1b carbohydrate chain. Identification of a potential host cell receptor for MCPyV will aid in the elucidation of its entry mechanism and pathophysiology.


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