The Centre for Dermatology Research, Institute of Inflammation and Repair, University of Manchester, Oxford Road, Stopford Building, Manchester, M13 9PT, U.K.
Crown Cosma Clinic, Thorley House, Bailey Lane, Manchester, U.K.
Br J Dermatol. 2015 Jun;172(6):1562-1572. doi: 10.1111/bjd.13549. Epub 2015 Mar 19.
ATP-binding cassette (ABC) transporters are involved in the active transport of an extremely diverse range of substrates across biological membranes. These transporters are commonly implicated in the development of multidrug resistance and are also involved in numerous physiological and homeostatic processes, including lipid transport, cell migration and differentiation.
To close the knowledge gap in the expression of ABC transporters in the human hair follicle (HF).
Quantitative polymerase chain reaction (qPCR) of ABC genes and immunofluorescence microscopy analysis of cryosections of human HFs.
By qPCR analysis, numerous members of the ABC transporter superfamily, such as ABCB1, ABCG2 and ABCA12, were found to be transcribed in full-length human scalp HFs. Immunofluorescence microscopy demonstrated that the intrafollicular protein expression of different xenobiotic ABC transporters (ABCB1, ABCC1, ABCC4, ABCG2) varies greatly, with ABCG2 expression restricted primarily to the epithelial stem cell region of the outer root sheath (bulge), whereas expression of ABCB1, ABCC1 and ABCC4 was more widespread. Lipid transporters ABCA1, ABCA12 and ABCA4 were almost uniformly expressed throughout the HF epithelium. Functional ABCB1/G2 activity was demonstrated by exclusion of the substrate dye, Hoechst 33342. In the bulge, this was reversed by ABCB1 and ABCG2 inhibition.
These data encourage further investigation of ABC transporters as potentially important regulators of HF epithelial biology. Clinically, pharmacological modulation of the activity of selected intrafollicular ABC transporters may permit novel therapeutic interventions, such as protecting HF stem cells from chemotherapy-induced damage, counteracting cholesterol-associated hypertrichosis, and manipulating the intrafollicular prostaglandin balance in androgenetic alopecia.
三磷酸腺苷结合盒(ABC)转运蛋白参与生物膜上各种底物的主动转运。这些转运蛋白通常与多药耐药的发展有关,并且还参与许多生理和动态平衡过程,包括脂质转运、细胞迁移和分化。
填补人类毛囊中 ABC 转运蛋白表达的知识空白。
采用定量聚合酶链反应(qPCR)检测 ABC 基因,并对人毛囊的冷冻切片进行免疫荧光显微镜分析。
通过 qPCR 分析,发现 ABC 转运蛋白超家族的许多成员,如 ABCB1、ABCG2 和 ABCA12,在全长人头皮毛囊中均有转录。免疫荧光显微镜显示,不同外源性 ABC 转运蛋白(ABCB1、ABCC1、ABCC4、ABCG2)的毛囊内蛋白表达差异很大,ABCG2 表达主要局限于外根鞘(隆起)的上皮干细胞区,而 ABCB1、ABCC1 和 ABCC4 的表达则更为广泛。脂质转运蛋白 ABCA1、ABCA12 和 ABCA4 在整个毛囊上皮中几乎均匀表达。通过排除底物染料 Hoechst 33342 证明了功能性 ABCB1/G2 活性。在隆起处,ABCB1 和 ABCG2 的抑制作用逆转了这一现象。
这些数据鼓励进一步研究 ABC 转运蛋白作为毛囊上皮生物学的潜在重要调节因子。临床上,选择性毛囊内 ABC 转运蛋白活性的药物调节可能允许新的治疗干预,例如保护毛囊干细胞免受化疗引起的损伤、对抗胆固醇相关的多毛症,以及在雄激素性脱发中调节毛囊内前列腺素平衡。