Gulf Coast Biologics, A Non-Profit Organization, Fort Myers, FL 33916, USA.
OrthoRegen Group, Max-Planck University, Indaiatuba 13334-170, SP, Brazil.
Int J Mol Sci. 2024 Jul 19;25(14):7914. doi: 10.3390/ijms25147914.
Autologous platelet-rich plasma (PRP) preparations are prepared at the point of care. Centrifugation cellular density separation sequesters a fresh unit of blood into three main fractions: a platelet-poor plasma (PPP) fraction, a stratum rich in platelets (platelet concentrate), and variable leukocyte bioformulation and erythrocyte fractions. The employment of autologous platelet concentrates facilitates the biological potential to accelerate and support numerous cellular activities that can lead to tissue repair, tissue regeneration, wound healing, and, ultimately, functional and structural repair. Normally, after PRP preparation, the PPP fraction is discarded. One of the less well-known but equally important features of PPP is that particular growth factors (GFs) are not abundantly present in PRP, as they reside outside of the platelet alpha granules. Precisely, insulin-like growth factor-1 (IGF-1) and hepatocyte growth factor (HGF) are mainly present in the PPP fraction. In addition to their roles as angiogenesis activators, these plasma-based GFs are also known to inhibit inflammation and fibrosis, and they promote keratinocyte migration and support tissue repair and wound healing. Additionally, PPP is known for the presence of exosomes and other macrovesicles, exerting cell-cell communication and cell signaling. Newly developed ultrafiltration technologies incorporate PPP processing methods by eliminating, in a fast and efficient manner, plasma water, cytokines, molecules, and plasma proteins with a molecular mass (weight) less than the pore size of the fibers. Consequently, a viable and viscous protein concentrate of functional total proteins, like fibrinogen, albumin, and alpha-2-macroglobulin is created. Consolidating a small volume of high platelet concentrate with a small volume of highly concentrated protein-rich PPP creates a protein-rich, platelet-rich plasma (PR-PRP) biological preparation. After the activation of proteins, mainly fibrinogen, the PR-PRP matrix retains and facilitates interactions between invading resident cells, like macrophages, fibroblast, and mesenchymal stem cells (MSCs), as well as the embedded concentrated PRP cells and molecules. The administered PR-PRP biologic will ultimately undergo fibrinolysis, leading to a sustained release of concentrated cells and molecules that have been retained in the PR-PRP matrix until the matrix is dissolved. We will discuss the unique biological and tissue reparative and regenerative properties of the PR-PRP matrix.
自体富含血小板血浆 (PRP) 制剂在治疗点制备。离心细胞密度分离将新鲜的血液单位分离成三个主要部分:血小板贫乏的血浆 (PPP) 部分、富含血小板的层 (血小板浓缩物) 和可变白细胞生物制剂和红细胞部分。使用自体血小板浓缩物有利于加速和支持许多细胞活动的生物学潜力,这些活动可以导致组织修复、组织再生、伤口愈合,最终实现功能和结构修复。通常,PRP 制备后,PPP 部分被丢弃。PPP 的一个不太为人知但同样重要的特点是,特定的生长因子 (GF) 在 PRP 中并不丰富存在,因为它们位于血小板 alpha 颗粒之外。确切地说,胰岛素样生长因子-1 (IGF-1) 和肝细胞生长因子 (HGF) 主要存在于 PPP 部分。除了作为血管生成激活剂的作用外,这些基于血浆的 GFs 还已知具有抑制炎症和纤维化的作用,并促进角质形成细胞迁移,支持组织修复和伤口愈合。此外,PPP 以存在外泌体和其他大囊泡而闻名,它们发挥细胞-细胞通讯和细胞信号作用。新开发的超滤技术通过快速有效地去除分子量(重量)小于纤维孔径的血浆水、细胞因子、分子和血浆蛋白,纳入 PPP 处理方法。因此,创建了一种可行且粘稠的功能性总蛋白(如纤维蛋白原、白蛋白和 α-2-巨球蛋白)蛋白浓缩物。将少量高血小板浓缩物与少量高浓度富含蛋白质的 PPP 合并,可创建富含蛋白质的富含血小板的 PRP 生物制剂。在主要是纤维蛋白原的蛋白质被激活后,PR-PRP 基质保留并促进浸润的常驻细胞(如巨噬细胞、成纤维细胞和间充质干细胞 (MSC))以及嵌入的浓缩 PRP 细胞和分子之间的相互作用。施用的 PR-PRP 生物制剂最终将经历纤维蛋白溶解,导致浓缩细胞和分子的持续释放,这些细胞和分子一直保留在 PR-PRP 基质中,直到基质溶解。我们将讨论 PR-PRP 基质的独特生物学和组织修复和再生特性。