The role of catecholamines in mesenchymal stem cell fate
- PMID: 25173883
- DOI: 10.1007/s00441-014-1984-8
The role of catecholamines in mesenchymal stem cell fate
Abstract
Mesenchymal stem cells (MSCs) are multipotent stem cells found in many adult tissues, especially bone marrow (BM) and are capable of differentiation into various lineage cells such as osteoblasts, adipocytes, chondrocytes and myocytes. Moreover, MSCs can be mobilized from connective tissue into circulation and from there to damaged sites to contribute to regeneration processes. MSCs commitment and differentiation are controlled by complex activities involving signal transduction through cytokines and catecholamines. There has been an increasing interest in recent years in the neural system, functioning in the support of stem cells like MSCs. Recent efforts have indicated that the catecholamine released from neural and not neural cells could be affected characteristics of MSCs. However, there have not been review studies of most aspects involved in catecholamines-mediated functions of MSCs. Thus, in this review paper, we will try to describe the current state of catecholamines in MSCs destination and discuss strategies being used for catecholamines for migration of these cells to damaged tissues. Then, the role of the nervous system in the induction of osteogenesis, adipogenesis, chondrogenesis and myogenesis from MSCs is discussed. Recent progress in studies of signaling transduction of catecholamines in determination of the final fate of MSCs is highlighted. Hence, the knowledge of interaction between MSCs with the neural system could be applied towards the development of new diagnostic and treatment alternatives for human diseases.
Similar articles
-
Pax3 activation promotes the differentiation of mesenchymal stem cells toward the myogenic lineage.Exp Cell Res. 2008 May 1;314(8):1721-33. doi: 10.1016/j.yexcr.2008.02.016. Epub 2008 Mar 5. Exp Cell Res. 2008. PMID: 18395202
-
Fate decision of mesenchymal stem cells: adipocytes or osteoblasts?Cell Death Differ. 2016 Jul;23(7):1128-39. doi: 10.1038/cdd.2015.168. Epub 2016 Feb 12. Cell Death Differ. 2016. PMID: 26868907 Free PMC article. Review.
-
Preferential therapy for osteoarthritis by cord blood MSCs through regulation of chondrogenic cytokines.Biomaterials. 2013 Jul;34(20):4739-48. doi: 10.1016/j.biomaterials.2013.03.016. Epub 2013 Apr 1. Biomaterials. 2013. PMID: 23557858
-
Dynamic expression characteristics of Notch signal in bone marrow-derived mesenchymal stem cells during the process of differentiation into hepatocytes.Tissue Cell. 2013 Apr;45(2):95-100. doi: 10.1016/j.tice.2012.09.008. Epub 2012 Oct 30. Tissue Cell. 2013. PMID: 23116754
-
Immunomodulatory Effect of Cytokines in the Differentiation of Mesenchymal Stem Cells: A Review.Curr Stem Cell Res Ther. 2017;12(3):197-206. doi: 10.2174/1574888X11666160614103404. Curr Stem Cell Res Ther. 2017. PMID: 27306400 Review.
Cited by
-
Mesenchymal Stem Cells after Polytrauma: Actor and Target.Stem Cells Int. 2016;2016:6289825. doi: 10.1155/2016/6289825. Epub 2016 Jun 2. Stem Cells Int. 2016. PMID: 27340408 Free PMC article. Review.
-
GPCRs in the regulation of the functional activity of multipotent mesenchymal stromal cells.Front Cell Dev Biol. 2022 Aug 15;10:953374. doi: 10.3389/fcell.2022.953374. eCollection 2022. Front Cell Dev Biol. 2022. PMID: 36046341 Free PMC article. Review.
-
β-Adrenergic Signal and Epigenomic Regulatory Process for Adaptive Thermogenesis.Adv Exp Med Biol. 2024;1461:213-227. doi: 10.1007/978-981-97-4584-5_15. Adv Exp Med Biol. 2024. PMID: 39289284 Review.
-
Fracture healing research: Recent insights.Bone Rep. 2023 May 19;19:101686. doi: 10.1016/j.bonr.2023.101686. eCollection 2023 Dec. Bone Rep. 2023. PMID: 38163010 Free PMC article. Review.
-
Combination of 5-fluorouracil and 2-morphilino-8-phenyl-4H-chromen-4-one may inhibit liver cancer stem cell activity.Tumour Biol. 2016 Aug;37(8):10943-58. doi: 10.1007/s13277-016-4915-3. Epub 2016 Feb 17. Tumour Biol. 2016. PMID: 26886287
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources