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通过脂联素和前列腺素对骨髓培养中脂肪细胞形成的旁分泌调节。

Paracrine regulation of fat cell formation in bone marrow cultures via adiponectin and prostaglandins.

作者信息

Yokota Takafumi, Meka C S Reddy, Medina Kay L, Igarashi Hideya, Comp Phillip C, Takahashi Masahiko, Nishida Makoto, Oritani Kenji, Miyagawa Jun-Ichiro, Funahashi Tohru, Tomiyama Yoshiaki, Matsuzawa Yuji, Kincade Paul W

机构信息

Immunobiology and Cancer Program, Oklahoma Medical Research Foundation, Oklahoma City 73104, USA.

出版信息

J Clin Invest. 2002 May;109(10):1303-10. doi: 10.1172/JCI14506.

Abstract

Adiponectin, an adipocyte-derived hormone, was recently shown to have potential therapeutic applications in diabetes and obesity because of its influence on glucose and lipid metabolism. We found that brown fat in normal human bone marrow contains this protein and used marrow-derived preadipocyte lines and long-term cultures to explore potential roles in hematopoiesis. Recombinant adiponectin blocked fat cell formation in long-term bone marrow cultures and inhibited the differentiation of cloned stromal preadipocytes. Adiponectin also caused elevated expression of cyclooxygenase-2 (COX-2) by these stromal cells and induced release of prostaglandin E(2) (PGE(2)). The COX-2 inhibitor Dup-697 prevented the inhibitory action of adiponectin on preadipocyte differentiation, suggesting involvement of stromal cell-derived prostanoids. Furthermore, adiponectin failed to block fat cell generation when bone marrow cells were derived from B6,129S(Ptgs2tm1Jed) (COX-2(+/-)) mice. These observations show that preadipocytes represent direct targets for adiponectin action, establishing a paracrine negative feedback loop for fat regulation. They also link adiponectin to the COX-2-dependent PGs that are critical in this process.

摘要

脂联素是一种由脂肪细胞分泌的激素,最近的研究表明,由于其对葡萄糖和脂质代谢的影响,它在糖尿病和肥胖症的治疗中具有潜在的应用价值。我们发现,正常人类骨髓中的棕色脂肪含有这种蛋白质,并利用骨髓来源的前脂肪细胞系和长期培养物来探索其在造血过程中的潜在作用。重组脂联素可阻断长期骨髓培养中的脂肪细胞形成,并抑制克隆的基质前脂肪细胞的分化。脂联素还可使这些基质细胞中环氧合酶-2(COX-2)的表达升高,并诱导前列腺素E2(PGE2)的释放。COX-2抑制剂Dup-697可阻止脂联素对前脂肪细胞分化的抑制作用,提示基质细胞衍生的前列腺素参与其中。此外,当骨髓细胞来自B6,129S(Ptgs2tm1Jed)(COX-2(+/-))小鼠时,脂联素无法阻断脂肪细胞的生成。这些观察结果表明,前脂肪细胞是脂联素作用的直接靶点,从而建立了一个脂肪调节的旁分泌负反馈回路。它们还将脂联素与在此过程中起关键作用的COX-2依赖性前列腺素联系起来。

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