Persson-Augner David, Lee Yong-Woo, Tovar Sulay, Dieguez Carlos, Meister Björn
Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Neuroendocrinology. 2014;100(2-3):209-20. doi: 10.1159/000369069. Epub 2014 Oct 20.
Delta-like 1 homologue (DLK1; also called preadipocyte factor 1) is an epidermal growth factor repeat-containing transmembrane protein that is cleaved by tumor necrosis factor-α-converting enzyme to generate a biologically active soluble form. DLK1 is involved in the differentiation of several cell types, including adipocytes. Lack of the dlk1 gene results in adiposity, and polymorphism within the gene encoding DLK1 is associated with human obesity. The dlk1 gene is expressed in restricted areas of the adult brain, with an enrichment of cell bodies expressing DLK1 mRNA in the hypothalamus. Antibodies to DLK1 were used to study the cellular localization and chemical identity of DLK1-immunoreactive neuronal cell bodies in rat hypothalamus. DLK1 immunoreactivity was demonstrated in the cell soma and dendrites of cell bodies in the suprachiasmatic, supraoptic, paraventricular, dorsomedial, arcuate nuclei and in the perifornical/lateral hypothalamic area. In the arcuate nucleus (Arc), DLK1 immunoreactivity was mainly seen in many neurons of the ventromedial and to a lesser extent in its ventrolateral division. Double labeling showed that 93.7% of orexigenic agouti-related peptide (AgRP) and 94.1% of neuropeptide Y (NPY) neurons located in the ventromedial part of the Arc were DLK1 positive, whereas 36.1% of anorexigenic pro-opiomelanocortin and 34.6% of cocaine- and amphetamine-regulated transcript neurons of the Arc contained DLK1 immunoreactivity. DLK1 mRNA was downregulated in the hypothalamus of fasted animals. Presence of DLK1 in the majority of orexigenic Arc NPY/AgRP neurons and regulation of DLK1 mRNA by nutritional challenge suggest that DLK1 has a role in hypothalamic regulation of body weight control. © 2014 S. Karger AG, Basel.
Delta样1同源物(DLK1;也称为前脂肪细胞因子1)是一种含有表皮生长因子重复序列的跨膜蛋白,可被肿瘤坏死因子-α转换酶切割,产生具有生物活性的可溶性形式。DLK1参与多种细胞类型的分化,包括脂肪细胞。dlk1基因的缺失会导致肥胖,并且编码DLK1的基因内的多态性与人类肥胖有关。dlk1基因在成年大脑的特定区域表达,下丘脑中有丰富的表达DLK1 mRNA的细胞体。使用针对DLK1的抗体来研究大鼠下丘脑DLK1免疫反应性神经元细胞体的细胞定位和化学特性。在视交叉上核、视上核、室旁核、背内侧核、弓状核以及穹窿周/下丘脑外侧区的细胞体的胞体和树突中均显示出DLK1免疫反应性。在弓状核(Arc)中,DLK1免疫反应性主要见于腹内侧的许多神经元,在其腹外侧部分的表达较少。双重标记显示,位于Arc腹内侧部分的93.7%的促食欲刺鼠相关肽(AgRP)神经元和94.1%的神经肽Y(NPY)神经元为DLK1阳性,而Arc中36.1%的厌食性阿黑皮素原和34.6%的可卡因和苯丙胺调节转录物神经元含有DLK1免疫反应性。禁食动物的下丘脑DLK1 mRNA表达下调。大多数促食欲的Arc NPY/AgRP神经元中存在DLK1以及营养刺激对DLK1 mRNA的调节表明,DLK1在体重控制的下丘脑调节中发挥作用。© 2014 S. Karger AG,巴塞尔。