Subramani Priya, Kannaiyan Jaianand, Rajabathar Jothi Ramalingam, Paulpandian Prema, Kamatchi Ramesh Kumar, Paulraj Balaji, Al-Lohedan Hamad A, Arokiyaraj Selvaraj, Veeramani Veeramanikandan
PG and Research Centre in Microbiology, MGR College, Hosur 635130 Tamil Nadu, India.
Research and Development, CellCure Therapeutics, Madurai 624217, Tamil Nadu, India.
ACS Omega. 2021 Dec 16;6(51):35538-35547. doi: 10.1021/acsomega.1c05022. eCollection 2021 Dec 28.
Mesenchymal stromal cells (MSCs) were isolated from (DB) and studied for their final cellular product measures, such as safety, purity, quality, quantity, and integrity that are ascribed as cellular products. This research aimed to isolate MSCs for expansion under the clinical scale level with potency, secretion of cytokines, growth factors secreted by DB-MSCs, and their role in wound healing. Placentas isolated from DB were expanded up to the 10th passage, and their characteristics were assessed by phenotypic characterization using a flow cytometer and analyzed for trilineage differentiation by cytochemical staining. Growth factors (GF), interleukins (IL), chemokines, and tissue inhibitors of metalloproteinases (TIMP) were measured with enzyme-linked immunosorbent assays. The harvested cells from the placenta yield 1.63-2.45 × 10cells/cm at P(0), 3.66-5.31 × 10cells/cm at P(1), 4.01-5.47 × 10cells/cm at P(2), and 3.94-5.60 × 10cells/cm at P(10) accordingly; up to 4.74 × 10 P(2) DB-MSCs were harvested within 9-11 days. The viability of the freshly harvested cells was greater than 90% in all cases. It is able to differentiate into chondrocytes, adipocytes, and osteogenic cells, proving their ability to differentiate into a trilineage. Thus, this study put an insight into a secure and conventional approach toward their ability to differentiate into multiple lineages and secrete factors related to immune regulation, making DB-MSCs a potential source in various therapeutic applications.
间充质基质细胞(MSCs)从[具体来源未明确,推测为DB相关组织]中分离出来,并对其作为细胞产品的最终细胞产物指标进行研究,如安全性、纯度、质量、数量和完整性。本研究旨在分离MSCs以在临床规模水平进行扩增,研究其效力、细胞因子分泌、DB - MSCs分泌的生长因子及其在伤口愈合中的作用。从DB分离的胎盘扩增至第10代,通过流式细胞仪进行表型鉴定评估其特征,并通过细胞化学染色分析其三系分化情况。采用酶联免疫吸附测定法测量生长因子(GF)、白细胞介素(IL)、趋化因子和金属蛋白酶组织抑制剂(TIMP)。胎盘收获的细胞在P(0)时产量为1.63 - 2.45×10[具体单位未明确]细胞/cm,P(1)时为3.66 - 5.31×10[具体单位未明确]细胞/cm,P(2)时为4.01 - 5.47×10[具体单位未明确]细胞/cm,P(10)时为3.94 - 5.60×10[具体单位未明确]细胞/cm;在9 - 11天内收获多达4.74×10[具体单位未明确]P(2)的DB - MSCs。所有情况下新鲜收获细胞的活力均大于90%。它能够分化为软骨细胞、脂肪细胞和成骨细胞,证明了其向三系分化的能力。因此,本研究深入探讨了一种安全且传统的方法,以了解其向多个谱系分化并分泌与免疫调节相关因子的能力,使DB - MSCs成为各种治疗应用中的潜在来源。