Cangyu Wang , Manxiu Cao , Junhong Zhao , Anqi Hu , Xiang Liu , Zihua Chen , Cuiping Zhang , Haihong Li
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Five weeks after implantation, the Matrigel plugs were harvested and the morphology and differentiation of the cells were examined by H&E staining and fluorescent immunohistochemical staining for ESG markers, such as Na+ -K+ -2Cl- cotransporter 1 (NKCC1), Na+ -K+ -ATPase (NKA), Foxa1 and K14.</span></p></div><div><h3>Results</h3><p>The epidermal cells and dermal cells of adult rat ventral foot skin can reconstruct 3D structure and express specific markers of ESGs in skin, such as NKCC1, NKA and Foxa1, indicating the ESG-phenotypic differentiation of the 3D structures. Double immunofluorescence<span> staining showed that some 3D structures expressed both the myoepithelial cell marker alpha-SMA and the common marker K14 of duct cells and myoepithelial cells, while some 3D structures expressed only K14, indicating that ESG-like 3D structures differentiated into duct-like and secretory coiled cells.</span></p></div><div><h3>Conclusion</h3><p>Epidermal and dermal cells from adult ESG-bearing skin can be used as a cell source for ESG regeneration.</p></div>","PeriodicalId":6961,"journal":{"name":"Acta histochemica","volume":"126 1","pages":"Article 152120"},"PeriodicalIF":2.3000,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Epidermal and dermal cells from adult rat eccrine sweat gland-containing skin can reconstruct the three-dimensional structure of eccrine sweat glands\",\"authors\":\"Cangyu Wang , Manxiu Cao , Junhong Zhao , Anqi Hu , Xiang Liu , Zihua Chen , Cuiping Zhang , Haihong Li\",\"doi\":\"10.1016/j.acthis.2023.152120\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>Previously, we have demonstrated that eccrine sweat gland cells (ESGCs) can reconstruct the three-dimensional (3D) structure of eccrine sweat glands (ESGs). 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Five weeks after implantation, the Matrigel plugs were harvested and the morphology and differentiation of the cells were examined by H&E staining and fluorescent immunohistochemical staining for ESG markers, such as Na+ -K+ -2Cl- cotransporter 1 (NKCC1), Na+ -K+ -ATPase (NKA), Foxa1 and K14.</span></p></div><div><h3>Results</h3><p>The epidermal cells and dermal cells of adult rat ventral foot skin can reconstruct 3D structure and express specific markers of ESGs in skin, such as NKCC1, NKA and Foxa1, indicating the ESG-phenotypic differentiation of the 3D structures. 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引用次数: 0
摘要
之前,我们已经证明了分泌汗腺细胞(ESGCs)可以重建分泌汗腺(esg)的三维(3D)结构。然而,仍然需要探索能够再生ESG的细胞来源,以解决ESG缺乏的情况下的ESG再生问题,如严重烧伤。方法分离成年大鼠腹足皮肤表皮细胞和真皮细胞。将分离的表皮细胞和真皮细胞与Matrigel混合,然后将混合物植入裸鼠腋窝/腹股沟脂肪垫。植入5周后,采集Matrigel桥塞,采用H&E染色和荧光免疫组化染色检测细胞ESG标志物Na+ - k + - 2cl - cotransporter 1 (NKCC1)、Na+ - k + - atpase (NKA)、Foxa1和K14的形态和分化情况。结果成年大鼠腹足皮肤表皮细胞和真皮细胞能够重建三维结构,并表达皮肤中特定的esg标记物NKCC1、NKA和Foxa1,提示三维结构的esg表型分化。双免疫荧光染色显示,部分3D结构既表达肌上皮细胞标记α - sma,也表达导管细胞和肌上皮细胞的共同标记K14,而部分3D结构仅表达K14,提示esg样3D结构向导管样和分泌型卷曲细胞分化。结论成人带ESG皮肤的表皮细胞和真皮细胞可作为ESG再生的细胞来源。
Epidermal and dermal cells from adult rat eccrine sweat gland-containing skin can reconstruct the three-dimensional structure of eccrine sweat glands
Background
Previously, we have demonstrated that eccrine sweat gland cells (ESGCs) can reconstruct the three-dimensional (3D) structure of eccrine sweat glands (ESGs). However, there is still a need to explore source cells capable of regenerating ESG to address the issue of ESG regeneration in ESGC-deficient conditions, such as severe burns.
Methods
The epidermal cells and dermal cells in adult rat ventral foot skin (ESG-bearing) were isolated. The isolated single epidermal cells and dermal cells were mixed with Matrigel, and then the mixture was implanted into the axillary/inguinal fat pads of nude mice. Five weeks after implantation, the Matrigel plugs were harvested and the morphology and differentiation of the cells were examined by H&E staining and fluorescent immunohistochemical staining for ESG markers, such as Na+ -K+ -2Cl- cotransporter 1 (NKCC1), Na+ -K+ -ATPase (NKA), Foxa1 and K14.
Results
The epidermal cells and dermal cells of adult rat ventral foot skin can reconstruct 3D structure and express specific markers of ESGs in skin, such as NKCC1, NKA and Foxa1, indicating the ESG-phenotypic differentiation of the 3D structures. Double immunofluorescence staining showed that some 3D structures expressed both the myoepithelial cell marker alpha-SMA and the common marker K14 of duct cells and myoepithelial cells, while some 3D structures expressed only K14, indicating that ESG-like 3D structures differentiated into duct-like and secretory coiled cells.
Conclusion
Epidermal and dermal cells from adult ESG-bearing skin can be used as a cell source for ESG regeneration.
期刊介绍:
Acta histochemica, a journal of structural biochemistry of cells and tissues, publishes original research articles, short communications, reviews, letters to the editor, meeting reports and abstracts of meetings. The aim of the journal is to provide a forum for the cytochemical and histochemical research community in the life sciences, including cell biology, biotechnology, neurobiology, immunobiology, pathology, pharmacology, botany, zoology and environmental and toxicological research. The journal focuses on new developments in cytochemistry and histochemistry and their applications. Manuscripts reporting on studies of living cells and tissues are particularly welcome. Understanding the complexity of cells and tissues, i.e. their biocomplexity and biodiversity, is a major goal of the journal and reports on this topic are especially encouraged. Original research articles, short communications and reviews that report on new developments in cytochemistry and histochemistry are welcomed, especially when molecular biology is combined with the use of advanced microscopical techniques including image analysis and cytometry. Letters to the editor should comment or interpret previously published articles in the journal to trigger scientific discussions. Meeting reports are considered to be very important publications in the journal because they are excellent opportunities to present state-of-the-art overviews of fields in research where the developments are fast and hard to follow. Authors of meeting reports should consult the editors before writing a report. The editorial policy of the editors and the editorial board is rapid publication. Once a manuscript is received by one of the editors, an editorial decision about acceptance, revision or rejection will be taken within a month. It is the aim of the publishers to have a manuscript published within three months after the manuscript has been accepted