Osteogenic Differentiation of Nucleus Pulposus Cells is Induced by Advanced Glycation End Products

2015 ◽  
Vol 15 (10) ◽  
pp. S186
Author(s):  
Svenja Illien-Junger
Keyword(s):  
Osteogenic Differentiation ◽  
Nucleus Pulposus ◽  
Advanced Glycation End Products ◽  
Advanced Glycation ◽  
Nucleus Pulposus Cells ◽  
Glycation End Products ◽  
End Products

scholarly journals Advanced glycation end products in degenerative nucleus pulposus with diabetes

2013 ◽  
Vol 32 (2) ◽  
pp. 238-244 ◽  
Author(s):  
Tsung-Ting Tsai ◽  
Natalie Yi-Ju Ho ◽  
Ying-Ting Lin ◽  
Po-Liang Lai ◽  
Tsai-Sheng Fu ◽  
...  
Keyword(s):  
Nucleus Pulposus ◽  
Advanced Glycation End Products ◽  
Advanced Glycation ◽  
Glycation End Products ◽  
End Products

Advanced glycation end-products downregulating intervertebral disc cell production of proteoglycans in vitro

2006 ◽  
Vol 5 (4) ◽  
pp. 324-329 ◽  
Author(s):  
Kimiaki Yokosuka ◽  
Jin Soo Park ◽  
Kotaro Jimbo ◽  
Kei Yamada ◽  
Kimiaki Sato ◽  
...  
Keyword(s):  
Intervertebral Disc ◽  
Nucleus Pulposus ◽  
Disc Degeneration ◽  
Advanced Glycation End Products ◽  
Immunohistochemical Analysis ◽  
Enzyme Linked Immunosorbent Assay ◽  
Advanced Glycation ◽  
Collagen Types ◽  
Glycation End Products ◽  
End Products

Object The authors sought to clarify the role, if any, of advanced glycation end-products (AGEs) in disc degeneration. Methods Intervertebral discs were analyzed for the presence of AGEs and of their receptor (RAGE) by immunohistochemical analysis. Reverse transcriptase polymerase chain reaction (RT-PCR) was performed to detect any RAGE gene expression, and real-time PCR was used to quantify messenger RNA (mRNA) levels of aggrecan and collagen types I and II in nucleus pulposus cells treated with AGEs. Aggrecan protein concentration was determined by enzyme-linked immunosorbent assay. Immunohistochemical analysis revealed that AGEs and RAGE were localized in the nucleus pulposus of the intervertebral disc. Advanced glycation end-products were found to significantly suppress the expression of aggrecan at both mRNA and protein levels in a dose- and time-dependent manner. The levels of collagen types I and II remained unchanged after treatments with AGEs. Conclusions These results suggest that the accumulation of AGEs and their interaction with their receptor in the nucleus pulposus might result in the downregulation of aggrecan production responsible for disc degeneration.

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