Department of Molecular Genetics.
Department of Radiation Oncology.
JCI Insight. 2018 Jul 26;3(14). doi: 10.1172/jci.insight.121221.
Cachexia syndrome consists of adipose and muscle loss, often despite normal food intake. We hypothesized that cachexia-associated adipose wasting is driven in part by tumor humoral factors that induce adipocyte lipolysis. We developed an assay to purify secreted factors from a cachexia-inducing colon cancer line that increases lipolysis in adipocytes and identified leukemia inhibitory factor (LIF) by mass spectrometry. Recombinant LIF induced lipolysis in vitro. Peripheral LIF administered to mice caused >50% loss of adipose tissue and >10% reduction in body weight despite only transient hypophagia due to decreasing leptin. LIF-injected mice lacking leptin (ob/ob) resulted in persistent hypophagia and loss of adipose tissue and body weight. LIF's peripheral role of initiating lipolysis in adipose loss was confirmed in pair-fed ob/ob mouse studies. Our studies demonstrate that (a) LIF is a tumor-secreted factor that promotes cachexia-like adipose loss when administered peripherally, (b) LIF directly induces adipocyte lipolysis, (c) LIF has the ability to sustain adipose and body weight loss through an equal combination of peripheral and central contributions, and (d) LIF's central effect is counterbalanced by decreased leptin signaling, providing insight into cachexia's wasting, despite normophagia.
恶病质综合征包括脂肪和肌肉减少,尽管通常摄入正常的食物。我们假设恶病质相关的脂肪丢失部分是由肿瘤体液因子引起的,这些因子诱导脂肪细胞脂解。我们开发了一种从诱导恶病质的结肠癌系中纯化分泌因子的测定法,该方法可增加脂肪细胞中的脂解作用,并通过质谱法鉴定白血病抑制因子(LIF)。重组 LIF 在体外诱导脂解。外周给予 LIF 会导致小鼠>50%的脂肪组织丢失和>10%的体重减轻,尽管由于瘦素减少仅导致短暂的食欲减退。注射 LIF 的缺乏瘦素的小鼠(ob/ob)导致持续的食欲减退和脂肪组织和体重减轻。在对喂养配对的 ob/ob 小鼠的研究中,证实了 LIF 在外周启动脂肪分解以引发脂肪丢失的作用。我们的研究表明:(a)LIF 是一种肿瘤分泌的因子,当外周给予时会促进恶病质样脂肪丢失;(b)LIF 直接诱导脂肪细胞脂解;(c)LIF 具有通过外周和中枢贡献相等组合维持脂肪和体重减轻的能力;(d)LIF 的中枢作用被降低的瘦素信号所抵消,这为尽管摄食正常但恶病质的消耗提供了深入了解。