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MD2 activation by direct AGE interaction drives inflammatory diabetic cardiomyopathy.


ABSTRACT: Hyperglycemia activates toll-like receptor 4 (TLR4) to induce inflammation in diabetic cardiomyopathy (DCM). However, the mechanisms of TLR4 activation remain unclear. Here we examine the role of myeloid differentiation 2 (MD2), a co-receptor of TLR4, in high glucose (HG)- and diabetes-induced inflammatory cardiomyopathy. We show increased MD2 in heart tissues of diabetic mice and serum of human diabetic subjects. MD2 deficiency in mice inhibits TLR4 pathway activation, which correlates with reduced myocardial remodeling and improved cardiac function. Mechanistically, we show that HG induces extracellular advanced glycation end products (AGEs), which bind directly to MD2, leading to formation of AGEs-MD2-TLR4 complex and initiation of pro-inflammatory pathways. We further detect elevated AGE-MD2 complexes in heart tissues and serum of diabetic mice and human subjects with DCM. In summary, we uncover a new mechanism of HG-induced inflammatory responses and myocardial injury, in which AGE products directly bind MD2 to drive inflammatory DCM.

SUBMITTER: Wang Y 

PROVIDER: S-EPMC7195432 | biostudies-literature | 2020 May

REPOSITORIES: biostudies-literature

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MD2 activation by direct AGE interaction drives inflammatory diabetic cardiomyopathy.

Wang Yi Y   Luo Wu W   Han Jibo J   Khan Zia A ZA   Fang Qilu Q   Jin Yiyi Y   Chen Xuemei X   Zhang Yali Y   Wang Meihong M   Qian Jianchang J   Huang Weijian W   Lum Hazel H   Wu Gaojun G   Liang Guang G  

Nature communications 20200501 1


Hyperglycemia activates toll-like receptor 4 (TLR4) to induce inflammation in diabetic cardiomyopathy (DCM). However, the mechanisms of TLR4 activation remain unclear. Here we examine the role of myeloid differentiation 2 (MD2), a co-receptor of TLR4, in high glucose (HG)- and diabetes-induced inflammatory cardiomyopathy. We show increased MD2 in heart tissues of diabetic mice and serum of human diabetic subjects. MD2 deficiency in mice inhibits TLR4 pathway activation, which correlates with red  ...[more]

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