Arteriogenesis and Therapeutic Angiogenesis

Although advances in therapeutic interventions improved outcomes, vascular occlusive diseases are still challenging not only afflicted but also attending physicians, requiring novel therapeutic strategies. Arteriogenesis, sometimes also called therapeutic angiogenesis, refers to the body's own...

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Bibliographic Details
Other Authors: Quax, Paul (Editor), Deindl, Elisabeth (Editor)
Format: Electronic Book Chapter
Language:English
Published: Basel MDPI - Multidisciplinary Digital Publishing Institute 2022
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DOAB: description of the publication
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520 |a Although advances in therapeutic interventions improved outcomes, vascular occlusive diseases are still challenging not only afflicted but also attending physicians, requiring novel therapeutic strategies. Arteriogenesis, sometimes also called therapeutic angiogenesis, refers to the body's own capacity to create a natural bypass around a narrowing or occluded arterial vessel. This book gives an insight into current knowledge and advances in vascular sciences and future prospects of therapeutic options. The utility and relevance of circulating biomarkers together with the potential of machine learning methods are discussed as well as the challenges and prospects of novel therapies such as protein- gene-, and stem cell therapy along with multicistronic multigene vectors and the use of microRNAs, exosomes, and secretomes. Vascular smooth muscle phenotype switch as a target to promote arteriogenesis is critically addressed, highlighting the problem of promoting atherosclerosis in parallel. Two articles even deal with cold-inducible RNA-binding protein CIRP/CIRPB presenting it as promising target to promote vascularization concomitant the reduction in ischemic tissue damage. BMPR kinase inhibition is introduced to improve tissue repair in a hereditary form of vascular disorder, and the role of the AP-1 transcription factor JunB in blood vessel formation is described. Some more experimental oriented articles deal with the relevance of choosing the appropriate mouse strain for investigations as well as in vitro Matrigel plug assay as a potent method to investigate angiogenesis. Last but not least, two-photon intravital microscopy is presented as suitable tool to assess plaque angiogenesis in atherosclerotic lesions. 
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650 7 |a Medicine  |2 bicssc 
653 |a angiogenesis 
653 |a vessel maturity 
653 |a vessel permeability 
653 |a hemorrhage 
653 |a atherosclerosis 
653 |a two-photon intravital microscopy 
653 |a transforming growth factor-β 
653 |a endoglin 
653 |a neovascularization 
653 |a tissue repair 
653 |a myocardial infarction 
653 |a hind limb ischemia 
653 |a critical limb ischemia 
653 |a arteriogenesis 
653 |a cell therapy 
653 |a secretomes 
653 |a AP-1 transcription factors 
653 |a JunB 
653 |a tip cell specification 
653 |a vascular development 
653 |a neurovascular interactions 
653 |a peripheral arterial disease 
653 |a biomarkers 
653 |a inflammation 
653 |a coagulation 
653 |a extracellular vesicles 
653 |a microRNAs 
653 |a machine learning 
653 |a gene therapy 
653 |a stem cells 
653 |a clinical trials 
653 |a bioengineering 
653 |a gene expression 
653 |a non-viral vectors 
653 |a 2A-peptides 
653 |a growth factors 
653 |a tube formation 
653 |a VEGF 
653 |a FGF2 
653 |a cytokines 
653 |a animal model 
653 |a Matrigel plug assay 
653 |a cold-inducible RNA-binding protein 
653 |a extracellular cold-inducible RNA-binding protein 
653 |a CIRP 
653 |a eCIRP 
653 |a neutrophil extracellular traps 
653 |a NETs 
653 |a macrophage polarization 
653 |a apoptosis 
653 |a ischemia 
653 |a vascular smooth muscle cell 
653 |a phenotypic switch 
653 |a collateral arteries 
653 |a C57BL/6J mice 
653 |a SV-129 mice 
653 |a leukocytes 
653 |a macrophages 
653 |a neutrophils 
653 |a C57BL6 
653 |a 129S1/Sv 
653 |a CIRBP 
653 |a 14q32 microRNAs 
653 |a HUVECs 
653 |a n/a 
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