Department of Orthopedic Surgery, SMG-SNU Boramae Medical Center, Seoul National University College of Medicine, Dongjak-Gu, Seoul, 07061, Korea.
Institute of Reproductive Medicine and Population, Medical Research Center at, Seoul National University, Jongno-Gu, Seoul, 03087, Korea.
Tissue Eng Regen Med. 2024 Dec;21(8):1217-1231. doi: 10.1007/s13770-024-00673-x. Epub 2024 Nov 5.
Tendinopathy is a chronic tendon disease. Mesenchymal stem cells (MSCs), known for their anti-inflammatory properties, may lose effectiveness with extensive culturing. Previous research introduced "small umbilical cord-derived fast proliferating cells" (smumf cells), isolated using a novel minimal cube explant method. These cells maintained their MSC characteristics through long-term culture. Thus, the purpose of the present study was to assess the anti-inflammatory effects of late-passage smumf cells at P10 on tenocytes derived from degenerative rotator cuff tears in a tendinopathic environment.
The mRNA expression with respect to aging of MSCs and secretion of growth factors (GFs) by smumf cells at P10 were measured. mRNA and protein synthesis in tenocytes with respect to the tenocyte phenotype, inflammatory cytokines, and matrix- degradation enzymes were measured. The inflammatory signal pathways involving nuclear factor kappa B (NF-κB) and mitogen-activated protein kinase (MAPK) in tenocytes were also investigated. The proliferative response of degenerative tenocytes to co-culture with smumf cells over 7 days in varying IL-1β induced tendinopathic environments was investigated.
smumf cells at P10 showed no signs of aging compared to those at P3. smumf cells at P10, secreting 2,043 pg/ml of hepatocyte growth factor (HGF), showed a 1.88-fold (p = .002) increase in HGF secretion in a tendinopathic environment. Degenerative tenocytes co-cultured with smumf cells showed significantly increased protein expression levels of collagen type I (Col I) and the Col I/III ratio by 1.46-fold (p < .001) and 1.66-fold (p < .001), respectively. The smumf cells at P10 reduced both mRNA and protein expression levels of matrix metalloproteinases-1, -2, -3, -8, -9, and -13 in tenocytes and attenuated NF-κB (phosphorylated IκBα/IκBα and phosphorylated p65/p65) and MAPK (phosphorylated p38/p38 and phosphorylated JNK/JNK) pathways activated by IL-1β. Removal of IL-1β from the co-culture accelerated the growth of tenocytes by 1.42-fold (p < .001). Removal of IL-1β accelerated tenocyte growth in co-cultures.
Late-passage smumf cells exert anti-inflammatory effects on tenocytes derived from degenerative rotator cuff tears under a tendinopathic environment, primarily through the secretion of growth factors (GFs).
腱病是一种慢性肌腱疾病。间充质干细胞(MSCs)以其抗炎特性而闻名,但在大量培养后可能会失去效力。先前的研究引入了“小脐带衍生的快速增殖细胞”(smumf 细胞),这些细胞是使用新型最小立方块外植体方法分离得到的。这些细胞通过长期培养保持其 MSC 特性。因此,本研究的目的是评估晚期传代 smumf 细胞(P10)对退行性肩袖撕裂在腱病环境中衍生的腱细胞的抗炎作用。
测量 P10 时 smumf 细胞的 MSC 衰老的 mRNA 表达和生长因子(GFs)的分泌情况。测量腱细胞中与腱细胞表型、炎症细胞因子和基质降解酶有关的 mRNA 和蛋白质合成。还研究了涉及核因子 kappa B(NF-κB)和丝裂原活化蛋白激酶(MAPK)的腱细胞中的炎症信号通路。在不同 IL-1β诱导的腱病环境中,7 天共培养过程中,退变腱细胞对与 smumf 细胞共培养的增殖反应进行了研究。
与 P3 相比,P10 时的 smumf 细胞没有衰老迹象。在腱病环境中,P10 时的 smumf 细胞分泌 2043pg/ml 的肝细胞生长因子(HGF),HGF 分泌增加 1.88 倍(p=.002)。与 smumf 细胞共培养的退变腱细胞的 I 型胶原(Col I)和 Col I/III 比值的蛋白表达水平分别显著增加 1.46 倍(p<.001)和 1.66 倍(p<.001)。P10 时的 smumf 细胞减少了腱细胞中基质金属蛋白酶-1、-2、-3、-8、-9 和 -13 的 mRNA 和蛋白表达水平,并减弱了 IL-1β 激活的 NF-κB(磷酸化 IκBα/IκBα 和磷酸化 p65/p65)和 MAPK(磷酸化 p38/p38 和磷酸化 JNK/JNK)通路。从共培养中去除 IL-1β 可使腱细胞的生长速度加快 1.42 倍(p<.001)。去除 IL-1β 可加速共培养中的腱细胞生长。
晚期传代 smumf 细胞对退行性肩袖撕裂在腱病环境下衍生的腱细胞具有抗炎作用,主要通过生长因子(GFs)的分泌。