Fujisaki Hitomi, Watanabe Takafumi, Yoshihara Shusuke, Fukuda Hideki, Tomono Yasuko, Tometsuka Chisa, Mizuno Kazunori, Nishiyama Toshio, Hattori Shunji
Nippi Research Institute of Biomatrix, 520-11 Kuwabara, Toride, Ibaraki 302-0017, Japan.
Laboratory of Veterinary Anatomy, School of Veterinary Medicine, Rakuno Gakuen University, Ebetsu, Hokkaido, Japan.
Regen Ther. 2024 Sep 3;26:717-728. doi: 10.1016/j.reth.2024.08.014. eCollection 2024 Jun.
Laminin 511 (LM511), a component of the skin basement membrane (BM), is known to enhance the adhesion of some cell types and it has been reported to affect cell behavior. A recombinant fragment consisting of the integrin recognition site; E8 region of LM511 (511E8) has also been studied. 511E8 has been reported by many as a superior culture substrate. However, the effects of 511E8 on human skin cells remain unclear. In this study, we added 511E8 during the culture period of a reconstituted skin equivalent (SE) and investigated its effect on the formation of BM-like structures.
SEs were formed by air-liquid culture of human foreskin keratinocytes (HFKs) on contracted type I collagen (Col-I) gels containing human fibroblasts. We compared the BM-like structures formed with and without 511E8 during HFKs culture periods. Morphological analysis, gene expression analysis of extracellular matrix components, and localization analysis of 511E8 in order to identify where 511E8 works were performed.
Immunohistochemical observation by light microscopy showed an accumulation of BM components between the gels and cell layers regardless of the addition of 511E8. There was a stronger and more continuous positive staining for LM α3, type IV collagen, and type VII collagen in the 511E8-added group compared to the no-added group. Transmission electron microscopic observation showed that the continuity of BM-like structures was increased with the addition of 511E8. Furthermore, gene expression analysis showed that the 511E8 addition increased some BM component genes expression, with collagen type IV and type VII α1 chains showing significant increases. His-tagged 511E8 was stained around the basal cells of HFK layers, not in basal regions. Co-staining with anti-His-tag and anti-integrin β1 antibodies revealed the co-localization of theses in some intercellular regions among basal cells.
These results suggest that 511E8 effected on HFKs, enhancing the production of BM components and strengthening the anchoring between the Col-I gels and the HFK layers.
层粘连蛋白511(LM511)是皮肤基底膜(BM)的一个组成部分,已知其可增强某些细胞类型的黏附力,并且据报道会影响细胞行为。一种由整合素识别位点组成的重组片段;LM511的E8区域(511E8)也已得到研究。许多人报道511E8是一种优质的培养底物。然而,511E8对人皮肤细胞的影响仍不清楚。在本研究中,我们在重组皮肤等效物(SE)的培养期间添加511E8,并研究其对类BM结构形成的影响。
通过在含有人类成纤维细胞的收缩型I型胶原蛋白(Col-I)凝胶上对人包皮角质形成细胞(HFK)进行气液培养来形成SE。我们比较了在HFK培养期间添加和不添加511E8时形成的类BM结构。进行了形态学分析、细胞外基质成分的基因表达分析以及511E8的定位分析,以确定511E8的作用位置。
光学显微镜下的免疫组织化学观察显示,无论是否添加511E8,凝胶和细胞层之间都有BM成分的积累。与未添加组相比,添加511E8的组中LMα3、IV型胶原蛋白和VII型胶原蛋白的阳性染色更强且更连续。透射电子显微镜观察显示,添加511E8后类BM结构的连续性增加。此外,基因表达分析表明,添加511E8会增加一些BM成分基因的表达,IV型胶原蛋白和VII型α1链显示出显著增加。带有His标签的511E8在HFK层的基底细胞周围染色,而不在基底区域。抗His标签抗体和抗整合素β1抗体的共染色显示,这些在基底细胞之间的一些细胞间区域共定位。
这些结果表明,511E8对HFK有影响,可增强BM成分的产生,并加强Col-I凝胶与HFK层之间的锚定。