Yang Qingqiu, Pinto Vanessa Marigo Rocha, Duan Wei, Paxton Erica E, Dessauer Jenna H, Ryan William, Lopez Mandi J
Laboratory for Equine and Comparative Orthopedic Research, Department of Veterinary Clinical Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA, United States.
Front Bioeng Biotechnol. 2019 Jul 11;7:155. doi: 10.3389/fbioe.2019.00155. eCollection 2019.
Damage to an ectodermal-mesodermal interface like that in the equine hoof and human finger nail bed can permanently alter tissue structure and associated function. The purpose of this study was to establish and validate culture of primary progenitor cell isolates from the ectodermal-mesodermal tissue junction in equine hooves, the stratum internum, with and without chronic inflammation known to contribute to lifelong tissue defects. The following were evaluated in hoof stratum internum cell isolates up to 5 cell passages (P): expansion capacity by cell doublings and doubling time; plasticity with multi-lineage differentiation and colony-forming unit (CFU) frequency percentage; immunophenotype with immunocytochemistry and flow cytometry; gene expression with RT-PCR; and ultrastructure with transmission electron microscopy. The presence of keratin (K)14, 15 and K19 as well as cluster of differentiation (CD)44 and CD29 was determined with immunohistochemistry. To confirm extracellular matrix (ECM) formation, cell-scaffold (polyethylene glycol/poly-L-lactic acid and tricalcium phosphate/hydroxyapatite) constructs were evaluated with scanning electron microscopy 9 weeks after implantation in athymic mice. Cultured cells had characteristic progenitor cell morphology, expansion, CFU frequency percentage and adipocytic, osteoblastic, and neurocytic differentiation capacity. CD44, CD29, K14, K15 and K19 proteins were present in native hoof stratum internum. Cultured cells also expressed K15, K19 and desmogleins 1 and 3. Gene expression of CD105, CD44, K14, K15, sex determining region Y-box 2 (SOX2) and octamer-binding transcription factor 4 (OCT4) was confirmed . Cultured cells had large, eccentric nuclei, elongated mitochondria, and intracellular vacuoles. Scaffold implants with cells contained fibrous ECM 9 weeks after implantation compared to little or none on acellular scaffolds. expansion and plasticity and ECM deposition of heterogeneous, immature cell isolates from the ectodermal-mesodermal tissue interface of normal and chronically inflamed hooves are typical of primary cell isolates from other adult tissues, and they appear to have both mesodermal and ectodermal qualities . These results establish a unique cell culture model to target preventative and restorative therapies for ectodermal-mesodermal tissue junctions.
像马的蹄子和人的指甲床中外胚层 - 中胚层界面的损伤会永久性地改变组织结构及相关功能。本研究的目的是建立并验证从马的蹄子的外胚层 - 中胚层组织交界处(即中层)分离出的原代祖细胞培养体系,该部位存在或不存在已知会导致终身组织缺陷的慢性炎症。对蹄中层细胞分离物进行了多达5代传代培养(P),并评估了以下指标:通过细胞倍增和倍增时间评估增殖能力;通过多谱系分化和集落形成单位(CFU)频率百分比评估可塑性;通过免疫细胞化学和流式细胞术评估免疫表型;通过逆转录 - 聚合酶链反应(RT - PCR)评估基因表达;通过透射电子显微镜评估超微结构。用免疫组织化学法测定角蛋白(K)14、15和K19以及分化簇(CD)44和CD29的存在情况。为了确认细胞外基质(ECM)的形成,在无胸腺小鼠体内植入9周后,用扫描电子显微镜评估细胞 - 支架(聚乙二醇/聚 - L - 乳酸和磷酸三钙/羟基磷灰石)构建体。培养的细胞具有典型的祖细胞形态、增殖能力、CFU频率百分比以及脂肪形成、成骨和神经细胞分化能力。CD44、CD29、K14、K15和K19蛋白存在于天然蹄中层中。培养的细胞还表达K15、K19以及桥粒芯糖蛋白1和3。证实了CD105、CD44、K14、K15、性别决定区Y盒2(SOX2)和八聚体结合转录因子4(OCT4)的基因表达。培养的细胞具有大的、偏心的细胞核、细长的线粒体和细胞内空泡。与无细胞支架相比,植入细胞的支架在植入9周后含有纤维状ECM。来自正常和慢性炎症蹄子的外胚层 - 中胚层组织界面的异质性、未成熟细胞分离物的增殖、可塑性和ECM沉积是其他成年组织原代细胞分离物的典型特征,并且它们似乎具有中胚层和外胚层的特性。这些结果建立了一个独特的细胞培养模型,用于针对外胚层 - 中胚层组织交界处的预防和修复治疗。