Albrecht E, Schering L, Liu Y, Komolka K, Kühn C, Wimmers K, Gotoh T, Maak S
J Anim Sci. 2017 May;95(5):2244-2254. doi: 10.2527/jas.2016.1036.
Appearance, distribution, and amount of intramuscular fat (IMF), often referred to as marbling, are highly variable and depend on environmental and genetic factors. On the molecular level, the concerted action of several drivers, including hormones, receptors, transcription factors, etc., determines where clusters of adipocytes arise. Therefore, the aim of future studies remains to identify such factors as biological markers of IMF to increase the ability to identify animals that deposit IMF early in age to increase efficiency of high-quality meat production. In an attempt to unravel the cellular development of marbling, we investigated the abundance of markers for adipogenic differentiation during fattening of cattle and the transcriptome of muscle and dissected IMF. Markers of different stages of adipogenic differentiation are well known from cell culture experiments. They are usually transiently expressed, such as delta-like homolog 1 (DLK1) that is abundant in preadipocytes and absent during differentiation to mature adipocytes. It is even a greater challenge to detect those markers in live animals. Within skeletal muscles, hyperplasia and hypertrophy of adipocytes can be observed throughout life. Therefore, development of marbling requires, on the cellular level, recruitment, proliferation, and differentiation of adipogenic cells to store excess energy in the form of lipids in new cells. In a recent study, we investigated the localization and abundance of early markers of adipogenic differentiation, such as DLK1, in bovine muscle tissue. An inverse relationship between IMF content and number of DLK1-positive cells in bovine muscle was demonstrated. Considering the cellular environment of differentiating adipocytes in muscle and the secretory action of adipocytes and myocytes, it becomes obvious that cross talk between cells via adipokines and myokines may be important for IMF development. Secreted proteins can act on other cells, inhibiting or stimulating their function via autocrine and paracrine actions. Such factors with potential influence on IMF, among them, agouti signaling protein and thrombospondin 4, were identified in transcriptome analyses and further investigated. Furthermore, results from transcriptome analysis indicate involvement of genes that are not directly related to adipogenesis and lipid metabolism, providing new candidates for future research.
肌内脂肪(IMF)的外观、分布和含量,通常称为大理石花纹,具有高度变异性,取决于环境和遗传因素。在分子水平上,包括激素、受体、转录因子等在内的多种驱动因素的协同作用决定了脂肪细胞簇的产生位置。因此,未来研究的目标仍然是确定这些因素作为IMF的生物标志物,以提高识别早期沉积IMF的动物的能力,从而提高优质肉类生产的效率。为了揭示大理石花纹的细胞发育过程,我们研究了牛育肥期间脂肪生成分化标志物的丰度以及肌肉和分离出的IMF的转录组。脂肪生成分化不同阶段的标志物在细胞培养实验中是众所周知的。它们通常是瞬时表达的,例如δ样同源物1(DLK1),在前脂肪细胞中含量丰富,在分化为成熟脂肪细胞的过程中消失。在活体动物中检测这些标志物是一个更大的挑战。在骨骼肌内,脂肪细胞的增生和肥大在整个生命过程中都可以观察到。因此,大理石花纹的形成在细胞水平上需要脂肪生成细胞的募集、增殖和分化,以便以脂质的形式在新细胞中储存多余的能量。在最近的一项研究中,我们研究了脂肪生成分化早期标志物,如DLK1,在牛肌肉组织中的定位和丰度。结果表明,牛肌肉中IMF含量与DLK1阳性细胞数量呈负相关。考虑到肌肉中分化脂肪细胞的细胞环境以及脂肪细胞和肌细胞的分泌作用,很明显,细胞间通过脂肪因子和肌因子的相互作用可能对IMF的发育很重要。分泌蛋白可以作用于其他细胞,通过自分泌和旁分泌作用抑制或刺激它们的功能。在转录组分析中鉴定出了此类对IMF有潜在影响的因子,其中包括刺鼠信号蛋白和血小板反应蛋白4,并对其进行了进一步研究。此外,转录组分析结果表明,一些与脂肪生成和脂质代谢不直接相关的基因也参与其中,为未来的研究提供了新的候选基因。