Napolitano Filomena, Giudice Valentina, D'Esposito Vittoria, Prevete Nella, Scala Pasqualina, de Paulis Amato, Selleri Carmine, Formisano Pietro, Rossi Francesca Wanda, Montuori Nunzia
Department of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.
Department of Medicine, Surgery and Dentistry "Scuola Medica Salernitana", University of Salerno, Salerno, Italy.
Front Cell Dev Biol. 2025 Feb 19;13:1518412. doi: 10.3389/fcell.2025.1518412. eCollection 2025.
Systemic Sclerosis (SSc) is a rare chronic systemic autoimmune disease characterized by fibrosis of the skin and internal organs and vasculopathy. Raynaud's phenomenon is typically the earliest clinical manifestation accompanied by skin inflammation, finger ulcers, and organ manifestations, including pulmonary fibrosis. There is an urgent need for the development of effective targeted therapeutic intervention for SSc patients. A greater focus has been placed on bioactive factors secreted by Mesenchymal Stem Cells (MSCs), with immunomodulatory and regenerative potentials. Current data report a different secretion profile of MSCs, depending on the tissue of origin. Understanding of the secretion profile of different MSCs is necessary to identify the most efficient and useful source for SSc treatment.
We analyzed the content of MSC-conditioned media (MSC-CM) obtained from MSCs isolated from adipose tissue (AT), bone marrow (BM), Wharton's jelly (WJ), and cord blood (CB) by ELISA method, and their effects on the wound healing process by fibroblast proliferation, migration, and ECM deposition assays, to compare regenerative potential of different MSC populations.
WJ-MSC-conditioned medium (CM) and BM-MSC-CM show a greater regenerative profile, compared to CB-MSC-CM and AT-MSC-CM, due to the abundance of growth factors and immunomodulatory cytokines and the effects on fibroblast functions. In SSc fibroblasts, WJ-MSC-CM significantly promotes fibroblast-mediated wound healing processes and VEGF expression, compared to BM-MSC-CM.
Our data indicate that WJ-MSC-CM could be considered an appealing strategy to both topical and systemic administrations in SSc patients.
系统性硬化症(SSc)是一种罕见的慢性全身性自身免疫性疾病,其特征为皮肤和内脏纤维化以及血管病变。雷诺现象通常是最早的临床表现,伴有皮肤炎症、手指溃疡和器官表现,包括肺纤维化。迫切需要为SSc患者开发有效的靶向治疗干预措施。人们更加关注间充质干细胞(MSCs)分泌的具有免疫调节和再生潜力的生物活性因子。目前的数据表明,MSCs的分泌谱因来源组织而异。了解不同MSCs的分泌谱对于确定SSc治疗最有效和有用的来源至关重要。
我们通过ELISA方法分析了从脂肪组织(AT)、骨髓(BM)、脐带胶质(WJ)和脐血(CB)分离的MSCs获得的MSC条件培养基(MSC-CM)的成分,并通过成纤维细胞增殖、迁移和细胞外基质沉积试验分析了它们对伤口愈合过程的影响,以比较不同MSC群体的再生潜力。
与CB-MSC-CM和AT-MSC-CM相比,WJ-MSC条件培养基(CM)和BM-MSC-CM显示出更大的再生能力,这归因于生长因子和免疫调节细胞因子的丰富以及对成纤维细胞功能的影响。在SSc成纤维细胞中,与BM-MSC-CM相比,WJ-MSC-CM显著促进成纤维细胞介导的伤口愈合过程和VEGF表达。
我们的数据表明,WJ-MSC-CM可被视为SSc患者局部和全身给药的一种有吸引力的策略。