Thomas Sachin, Jaganathan Bithiah Grace
Stem Cells and Cancer Biology Research Group, Department of Biosciences and Bioengineering, Indian Institute of Technology Guwahati, Guwahati, Assam, 781039, India.
J Cell Commun Signal. 2022 Mar;16(1):47-61. doi: 10.1007/s12079-021-00635-1. Epub 2021 Jul 8.
Osteogenesis is an important developmental event that results in bone formation. Bone forming cells or osteoblasts develop from mesenchymal stem cells (MSCs) through a highly controlled process regulated by several signaling pathways. The osteogenic lineage commitment of MSCs is controlled by cell-cell interactions, paracrine factors, mechanical signals, hormones, and cytokines present in their niche, which activate a plethora of signaling molecules belonging to bone morphogenetic proteins, Wnt, Hedgehog, and Notch signaling. These signaling pathways individually as well as in coordination with other signaling molecules, regulate the osteogenic lineage commitment of MSCs by activating several osteo-lineage specific transcription factors. Here, we discuss the key signaling pathways that regulate osteogenic differentiation of MSCs and the cross-talk between them during osteogenic differentiation. We also discuss how these signaling pathways can be modified for therapy for bone repair and regeneration.
骨生成是导致骨形成的重要发育事件。骨形成细胞或成骨细胞由间充质干细胞(MSC)通过受多种信号通路调控的高度可控过程发育而来。MSC向成骨谱系的定向分化受其微环境中细胞间相互作用、旁分泌因子、机械信号、激素和细胞因子的控制,这些因素激活了属于骨形态发生蛋白、Wnt、Hedgehog和Notch信号的大量信号分子。这些信号通路单独以及与其他信号分子协同作用,通过激活几种成骨谱系特异性转录因子来调节MSC向成骨谱系的定向分化。在此,我们讨论调节MSC成骨分化的关键信号通路以及它们在成骨分化过程中的相互作用。我们还讨论了如何对这些信号通路进行修饰以用于骨修复和再生治疗。