Kadoya Kuniko, Fukushi Jun-Ichi, Matsumoto Yoshihiro, Yamaguchi Yu, Stallcup William B
Burnham Institute for Medical Research, La Jolla, California, USA.
J Histochem Cytochem. 2008 Mar;56(3):295-303. doi: 10.1369/jhc.7A7349.2007. Epub 2007 Nov 26.
In early postnatal mouse skin, the NG2 proteoglycan is expressed in the subcutis, the dermis, the outer root sheath of hair follicles, and the basal keratinocyte layer of the epidermis. With further development, NG2 is most prominently expressed by stem cells in the hair follicle bulge region, as also observed in adult human skin. During telogen and anagen phases of the adult hair cycle, NG2 is also found in stem cell populations that reside in dermal papillae and the outer root sheaths of hair follicles. Ablation of NG2 produces alterations in both the epidermis and subcutis layers of neonatal skin. Compared with wild type, the NG2 null epidermis does not achieve its full thickness due to reduced proliferation of basal keratinocytes that serve as the stem cell population in this layer. Thickening of the subcutis is also delayed in NG2 null skin due to deficiencies in the adipocyte population.
在出生后早期的小鼠皮肤中,NG2蛋白聚糖在皮下组织、真皮、毛囊外根鞘以及表皮的基底角质形成细胞层中表达。随着进一步发育,NG2在毛囊隆突区的干细胞中表达最为显著,在成人皮肤中也观察到这种情况。在成人毛发周期的休止期和生长期,NG2也存在于位于真皮乳头和毛囊外根鞘的干细胞群体中。NG2的缺失会导致新生皮肤的表皮和皮下组织层发生改变。与野生型相比,NG2基因敲除的表皮由于作为该层干细胞群体的基底角质形成细胞增殖减少而未达到其全层厚度。由于脂肪细胞群体的缺陷,NG2基因敲除皮肤的皮下组织增厚也会延迟。