Gniadecki Robert, Bang Bo
Department of Dermatology D92, Bispebjerg Hospital, Bispebjerg bake 23, University of Copenhagen, DK-2400 Copenhagen NV, Denmark.
J Invest Dermatol. 2003 Sep;121(3):522-8. doi: 10.1046/j.1523-1747.2003.12419.x.
Lipid rafts are dynamic membrane microdomains enriched in cholesterol and sphingolipids and are involved in the regulation of a variety of cellular processes, such as proliferation, apoptosis and cell motility. We have previously described that large lipid raft aggregates are readily detectable on cultured keratinocyte cell line HaCaT by staining with the fluorescein-tagged cholera toxin (CTx-FITC). In this paper we adopted this method for the detection of lipid rafts in human epidermis and keratinocytes in culture. Double labelling of showed the non-overlapping clusters of basal cells in human epidermis: CD29dimCTx-FITCbright cells in the deep rate ridges and CD29brightCTx-FITCdim cells at the tips of dermal papillae. A similar patchy, non-overlapping staining pattern was observed in cultured keratinocytes in vitro. CTx-FITCbright cells are mitotically active whereas a large proportion of CTx-FITCdim cells are quiescent. We conclude that the epidermal stem-like cells, previously shown to occupy the tips of dermal papillae and to exhibit high density of membrane beta1 integrin have a low content of lipid rafts. In contrast, the putative transit amplifying cells in deep rate ridges show enrichment in lipid rafts. Thus, lipid rafts may be a factor controlling the mitotic activity of epidermal keratinocytes and possibly the differentiation of stem cells into the transit amplifying cells.
脂筏是富含胆固醇和鞘脂的动态膜微区,参与多种细胞过程的调控,如增殖、凋亡和细胞运动。我们之前曾描述过,通过用荧光素标记的霍乱毒素(CTx-FITC)染色,在培养的角质形成细胞系HaCaT上很容易检测到大型脂筏聚集体。在本文中,我们采用这种方法检测人表皮和培养的角质形成细胞中的脂筏。双重标记显示人表皮基底细胞的非重叠簇:在深部嵴中的CD29dimCTx-FITCbright细胞和在真皮乳头尖端的CD29brightCTx-FITCdim细胞。在体外培养的角质形成细胞中也观察到类似的斑驳、非重叠染色模式。CTx-FITCbright细胞具有有丝分裂活性,而大部分CTx-FITCdim细胞处于静止状态。我们得出结论,先前显示占据真皮乳头尖端并表现出高密度膜β1整合素的表皮干细胞样细胞的脂筏含量较低。相比之下,深部嵴中假定的过渡放大细胞显示脂筏富集。因此,脂筏可能是控制表皮角质形成细胞有丝分裂活性以及可能控制干细胞向过渡放大细胞分化的一个因素。