Cell Therapy for Critical Limb Ischemia: Advantages, Limitations, and New Perspectives for Treatment of Patients with Critical Diabetic Vasculopathy

被引:18
作者
Gu, Y. [1 ]
Rampin, A. [2 ]
Alvino, V. V. [1 ]
Spinetti, G. [2 ]
Madeddu, P. [1 ]
机构
[1] Univ Bristol, Bristol Med Sch, Translat Hlth Sci, Upper Maudlin St, Bristol BS2 8HW, Avon, England
[2] IRCCS, MultiMed, Lab Cardiovasc Res, Milan, Italy
关键词
Critical Limb Ischemia; Diabetes Mellitus; MicroRNAs; Microvesicles; Proangiogenic cells; Vascular Stem and Progenitor cells; ENDOTHELIAL PROGENITOR CELLS; PERIPHERAL ARTERIAL-DISEASE; MESENCHYMAL STROMAL CELLS; BONE-MARROW; STEM-CELL; OXIDATIVE STRESS; DOUBLE-BLIND; MOUSE MODEL; AUTOLOGOUS TRANSPLANTATION; VASCULAR COMPLICATIONS;
D O I
10.1007/s11892-021-01378-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of Review To provide a highlight of the current state of cell therapy for the treatment of critical limb ischemia in patients with diabetes. Recent Findings The global incidence of diabetes is constantly growing with consequent challenges for healthcare systems worldwide. In the UK only, NHS costs attributed to diabetic complications, such as peripheral vascular disease, amputation, blindness, renal failure, and stroke, average 10 pound billion each year, with cost pressure being estimated to get worse. Although giant leaps forward have been registered in the scope of early diagnosis and optimal glycaemic control, an effective treatment for critical limb ischemia is still lacking. The present review aims to provide an update of the ongoing work in the field of regenerative medicine. Recent advancements but also limitations imposed by diabetes on the potential of the approach are addressed. In particular, the review focuses on the perturbation of non-coding RNA networks in progenitor cells and the possibility of using emerging knowledge on molecular mechanisms to design refined protocols for personalized therapy. The field of cell therapy showed rapid progress but has limitations. Significant advances are foreseen in the upcoming years thanks to a better understanding of molecular bottlenecks associated with the metabolic disorders.
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页数:13
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共 145 条
[1]   The immune boundaries for stem cell based therapies: problems and prospective solutions [J].
Abdelkrim, Hmadcha ;
Juan, Dominguez-Bendala ;
Jane, Wakeman ;
Mohamed, Arredouani ;
Bernat, Soria .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2009, 13 (8A) :1464-1475
[2]   Akt1/protein kinase Bα is critical for ischemic and VEGF-mediated angiogenesis [J].
Ackah, E ;
Yu, J ;
Zoellner, S ;
Iwakiri, Y ;
Skurk, C ;
Shibata, R ;
Ouchi, N ;
Easton, RM ;
Galasso, G ;
Birnbaum, MJ ;
Walsh, K ;
Sessa, WC .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (08) :2119-2127
[3]   Role for Substance P-Based Nociceptive Signaling in Progenitor Cell Activation and Angiogenesis During Ischemia in Mice and in Human Subjects [J].
Amadesi, Silvia ;
Reni, Carlotta ;
Katare, Rajesh ;
Meloni, Marco ;
Oikawa, Atsuhiko ;
Beltrami, Antonio P. ;
Avolio, Elisa ;
Cesselli, Daniela ;
Fortunato, Orazio ;
Spinetti, Gaia ;
Ascione, Raimondo ;
Cangiano, Elisa ;
Valgimigli, Marco ;
Hunt, Stephen P. ;
Emanueli, Costanza ;
Madeddu, Paolo .
CIRCULATION, 2012, 125 (14) :1774-1786
[4]   miR-23c regulates wound healing by targeting stromal cell-derived factor-1α (SDF-1α/CXCL12) among patients with diabetic foot ulcer [J].
Amin, Karan Naresh ;
Umapathy, Dhamodharan ;
Anandharaj, Arunkumar ;
Ravichandran, Jayasuriya ;
Sasikumar, Changam Sheela ;
Chandra, Sathish Kumar Rajappan ;
Kesavan, Rajesh ;
Mohanram, Ramkumar Kunka .
MICROVASCULAR RESEARCH, 2020, 127
[5]   Abnormalities in Skeletal Muscle Myogenesis, Growth, and Regeneration in Myotonic Dystrophy [J].
Andre, Laurene M. ;
Ausems, C. Rosanne M. ;
Wansink, Derick G. ;
Wieringa, Be .
FRONTIERS IN NEUROLOGY, 2018, 9
[6]   Autologous immuno magnetically selected CD133+stem cells in the treatment of no-option critical limb ischemia: clinical and contrast enhanced ultrasound assessed results in eight patients [J].
Arici, Vittorio ;
Perotti, Cesare ;
Fabrizio, Calliada ;
Del Fante, Claudia ;
Ragni, Franco ;
Alessandrino, Francesco ;
Viarengo, Gianluca ;
Pagani, Michele ;
Moia, Alessia ;
Tinelli, Carmine ;
Bozzani, Antonio .
JOURNAL OF TRANSLATIONAL MEDICINE, 2015, 13
[7]   Pericytes: Developmental, Physiological, and Pathological Perspectives, Problems, and Promises [J].
Armulik, Annika ;
Genove, Guillem ;
Betsholtz, Christer .
DEVELOPMENTAL CELL, 2011, 21 (02) :193-215
[8]   Isolation of putative progenitor endothelial cells for angiogenesis [J].
Asahara, T ;
Murohara, T ;
Sullivan, A ;
Silver, M ;
vanderZee, R ;
Li, T ;
Witzenbichler, B ;
Schatteman, G ;
Isner, JM .
SCIENCE, 1997, 275 (5302) :964-967
[9]   MicroRNA-126 overexpression rescues diabetes-induced impairment in efferocytosis of apoptotic cardiomyocytes [J].
Babu, Sahana Suresh ;
Thandavarayan, Rajarajan A. ;
Joladarashi, Darukeshwara ;
Jeyabal, Prince ;
Krishnamurthy, Shashirekha ;
Bhimaraj, Arvind ;
Youker, Keith A. ;
Krishnamurthy, Prasanna .
SCIENTIFIC REPORTS, 2016, 6
[10]   Human CD133+ Progenitor Cells Promote the Healing of Diabetic Ischemic Ulcers by Paracrine Stimulation of Angiogenesis and Activation of Wnt Signaling [J].
Barcelos, Luciola S. ;
Duplaa, Cecile ;
Kraenkel, Nicolle ;
Graiani, Gallia ;
Invernici, Gloria ;
Katare, Rajesh ;
Siragusa, Mauro ;
Meloni, Marco ;
Campesi, Ilaria ;
Monica, Manuela ;
Simm, Andreas ;
Campagnolo, Paola ;
Mangialardi, Giuseppe ;
Stevanato, Lara ;
Alessandri, Giulio ;
Emanueli, Costanza ;
Madeddu, Paolo .
CIRCULATION RESEARCH, 2009, 104 (09) :1095-U199