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紫外线照射诱导的脂肪细胞趋化因子有助于损伤皮下脂肪细胞的脂肪代谢。

Adipochemokines induced by ultraviolet irradiation contribute to impaired fat metabolism in subcutaneous fat cells.

机构信息

Department of Dermatology, Seoul National University College of Medicine, Seoul, Republic of Korea.

Laboratory of Cutaneous Aging Research, Biomedical Research Institute, Seoul National University Hospital, Seoul, Republic of Korea.

出版信息

Br J Dermatol. 2018 Feb;178(2):492-501. doi: 10.1111/bjd.15907. Epub 2017 Dec 29.

Abstract

BACKGROUND

Adipose tissue is now appreciated as the pivotal regulator of metabolic and endocrine functions. Subcutaneous (SC) fat, in contrast to visceral fat, may protect against metabolic syndrome and systemic inflammation. We demonstrated that chronic as well as acute ultraviolet (UV) irradiation to the skin induces loss of underlying SC fat. UV-irradiated SC fat may produce chemokines or cytokines that modulate lipid homeostasis and secretion of adipokines.

OBJECTIVES

To elucidate UV-induced specific adipochemokines implicated in UV-induced modulation of SC fat.

METHODS

Primary cultured adipocytes were treated with conditioned medium from UV- or sham-irradiated skin cells. Young and older healthy participants provided SC fat from sun-exposed and sun-protected skin. Sun-protected skin from other participants was irradiated with UV. Differentially expressed adipochemokines were screened by cytokine array, and confirmed in vitro and in vivo. The functions of select adipochemokines involved in lipid metabolism were examined via short interfering RNA-mediated knockdown of cognate receptors.

RESULTS

Specific adipochemokines, including C-X-C motif chemokine (CXCL) family members such as CXCL5/ENA-78, and C-C motif chemokine (CCL) family members such as CCL20/MIP-3α and CCL5/RANTES, were greatly induced in SC fat by UV exposure. They could impair triglyceride synthesis via downregulation of lipogenic enzymes and sterol regulatory element-binding protein-1 through their respective cognate receptors, CXC chemokine receptor type (CXC-R)2, C-C chemokine receptor type (CCR)-6, and CCR-5. In addition, UV irradiation induced infiltration of adipose tissue macrophages responsible for the secretion of several chemokines into SC fat.

CONCLUSIONS

These UV-induced adipochemokines may be implicated in the reduction of lipogenesis in SC fat, leading to impairment of fat homeostasis and associated comorbidities such as obesity.

摘要

背景

脂肪组织现在被认为是调节代谢和内分泌功能的关键调节剂。与内脏脂肪相比,皮下(SC)脂肪可能有助于预防代谢综合征和全身炎症。我们发现,慢性和急性紫外线(UV)辐射皮肤会导致皮下 SC 脂肪丢失。UV 辐射的 SC 脂肪可能会产生趋化因子或细胞因子,从而调节脂质稳态和脂肪因子的分泌。

目的

阐明与 UV 诱导的 SC 脂肪调节相关的 UV 诱导的特定脂肪趋化因子。

方法

用条件培养基处理原代培养的脂肪细胞,该条件培养基来自 UV 或假照射的皮肤细胞。年轻和年长的健康参与者提供来自阳光照射和防晒皮肤的 SC 脂肪。来自其他参与者的防晒皮肤用 UV 照射。通过细胞因子阵列筛选差异表达的脂肪趋化因子,并在体外和体内进行验证。通过短干扰 RNA 介导的同源受体敲低,研究参与脂质代谢的选定脂肪趋化因子的功能。

结果

包括 C-X-C 基序趋化因子(CXCL)家族成员(如 CXCL5/ENA-78)和 C-C 基序趋化因子(CCL)家族成员(如 CCL20/MIP-3α 和 CCL5/RANTES)在内的特定脂肪趋化因子在 SC 脂肪中被 UV 暴露大大诱导。它们可以通过下调脂肪生成酶和固醇调节元件结合蛋白-1 来损害甘油三酯的合成,通过它们各自的同源受体 CXC 趋化因子受体类型(CXC-R)2、CC 趋化因子受体类型(CCR)-6 和 CCR-5。此外,UV 照射诱导脂肪组织巨噬细胞浸润 SC 脂肪,后者负责几种趋化因子的分泌。

结论

这些 UV 诱导的脂肪趋化因子可能与 SC 脂肪中脂肪生成减少有关,导致脂肪稳态受损,并与肥胖等相关的合并症有关。

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