Mapping the expression of epithelial hair follicle stem cell-related transcription factors LHX2 and SOX9 in the human hair follicle

被引:29
|
作者
Purba, Talveen S. [1 ]
Haslam, Iain S. [1 ]
Shahmalak, Asim [2 ]
Bhogal, Ranjit K. [3 ]
Paus, Ralf [1 ,4 ]
机构
[1] Univ Manchester, Inst Inflammat & Repair, Ctr Dermatol Res, Manchester M13 9PT, Lancs, England
[2] Crown Clin, Manchester, Lancs, England
[3] Unilever R&D Colworth, Sharnbrook MK44 1LQ, Beds, England
[4] Univ Munster, Dept Dermatol, D-48149 Munster, Germany
基金
英国生物技术与生命科学研究理事会;
关键词
eHFSCs; epithelial human hair follicle stem cells; K15; K19; LHX2; SOX9; OUTER ROOT SHEATH; DIFFERENTIAL EXPRESSION; NICHE; CARCINOMA; MARKERS; PROLIFERATION; SPECIFICATION; DEFINES; GENE; LGR5;
D O I
10.1111/exd.12700
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
In the murine hair follicle (HF), the transcription factors LHX2 and SOX9 are implicated in epithelial hair follicle stem cell (eHFSC) self-renewal and the maintenance of eHFSC niche characteristics. However, the exact expression patterns of LHX2 and SOX9 in the human HF are unclear. Therefore, we have quantitatively mapped the localisation of known human eHFSC markers keratin 15 (K15) and keratin 19 (K19) in the outer root sheath (ORS) of male occipital scalp anagen HFs and related this to the localisation of LHX2 and SOX9 protein expression. As expected, K15(+) and K19(+) cells represented two distinct progenitor cell populations in the bulge and in the proximal bulb ORS (pbORS). Interestingly, cell fluorescence for K19 was significantly stronger within the pbORS versus the bulge, and vice versa for K15, describing a hitherto unrecognised differential expression pattern. LHX2 and SOX9 expressing cells were distributed throughout the ORS, including the bulge, but were not restricted to it. SOX9 expression was most prominent in the ORS immediately below the human bulge, whereas LHX2(+) cells were similarly distributed between the sub-bulge and pbORS, that is compartments not enriched with quiescent eHFSCs. During catagen development, the intensity of LHX2 and SOX9 protein expression increased in the proximal HF epithelium. Double immunostaining showed that the majority ofSOX9(+) cells in the human anagen HF epithelium did not co-express K15, K19 or LHX2. This expression profile suggests that LHX2 and SOX9 highlight distinct epithelial progenitor cell populations, in addition to K15(+) or K19(+) cells, that could play an important role in the maintenance of the human HF epithelium.
引用
收藏
页码:462 / 467
页数:6
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