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人类毛囊内部存在科里循环,并通过糖元磷酸化酶来调节其生长。

Human hair follicles operate an internal Cori cycle and modulate their growth via glycogen phosphorylase.

机构信息

Centre for Cell Biology and Cutaneous Research, Blizard Institute, Barts & The London School of Medicine and Dentistry, Queen Mary University of London, 4 Newark Street, London, E1 2AT, UK.

Farjo Hair Institute, London, UK.

出版信息

Sci Rep. 2021 Oct 21;11(1):20761. doi: 10.1038/s41598-021-99652-8.

Abstract

Hair follicles (HFs) are unique, multi-compartment, mini-organs that cycle through phases of active hair growth and pigmentation (anagen), apoptosis-driven regression (catagen) and relative quiescence (telogen). Anagen HFs have high demands for energy and biosynthesis precursors mainly fulfilled by aerobic glycolysis. Histochemistry reports the outer root sheath (ORS) contains high levels of glycogen. To investigate a functional role for glycogen in the HF we quantified glycogen by Periodic-Acid Schiff (PAS) histomorphometry and colorimetric quantitative assay showing ORS of anagen VI HFs contained high levels of glycogen that decreased in catagen. qPCR and immunofluorescence microscopy showed the ORS expressed all enzymes for glycogen synthesis and metabolism. Using human ORS keratinocytes (ORS-KC) and ex vivo human HF organ culture we showed active glycogen metabolism by nutrient starvation and use of a specific glycogen phosphorylase (PYGL) inhibitor. Glycogen in ORS-KC was significantly increased by incubation with lactate demonstrating a functional Cori cycle. Inhibition of PYGL significantly stimulated the ex vivo growth of HFs and delayed onset of catagen. This study defines translationally relevant and therapeutically targetable new features of HF metabolism showing that human scalp HFs operate an internal Cori cycle, synthesize glycogen in the presence of lactate and modulate their growth via PYGL activity.

摘要

毛囊(HFs)是独特的、多腔室的微型器官,经历生长期(生长期)、凋亡驱动的退行期(退行期)和相对静止期(休止期)的循环。生长期 HFs 对能量和生物合成前体的需求很高,主要通过有氧糖酵解来满足。组织化学报告外根鞘(ORS)含有高水平的糖原。为了研究糖原在 HF 中的功能作用,我们通过周期性酸-Schiff(PAS)组织形态计量法和比色定量测定法对糖原进行定量,结果显示生长期 VI HF 的 ORS 含有高水平的糖原,在退行期减少。qPCR 和免疫荧光显微镜显示 ORS 表达糖原合成和代谢的所有酶。使用人 ORS 角质形成细胞(ORS-KC)和离体人 HF 器官培养,我们通过营养饥饿和特定糖原磷酸化酶(PYGL)抑制剂的使用显示了活跃的糖原代谢。用乳酸孵育可显著增加 ORS-KC 中的糖原,证明存在功能性科里循环。PYGL 的抑制显著刺激了 HF 的离体生长并延迟了退行期的发生。这项研究定义了 HF 代谢的具有转化意义和治疗靶点的新特征,表明人头皮 HF 内运行着一个内部科里循环,在有乳酸的情况下合成糖原,并通过 PYGL 活性调节其生长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c3c/8531296/03a3b6f4955e/41598_2021_99652_Fig1_HTML.jpg

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