دورية أكاديمية

Immunoengineering strategies to enhance vascularization and tissue regeneration.

التفاصيل البيبلوغرافية
العنوان: Immunoengineering strategies to enhance vascularization and tissue regeneration.
المؤلفون: Zarubova J; Department of Bioengineering, University of California, Los Angeles, CA 90095, USA; Department of Biomaterials and Tissue Engineering, Institute of Physiology of the Czech Academy of Sciences, Prague 14220, Czech Republic., Hasani-Sadrabadi MM; Department of Bioengineering, University of California, Los Angeles, CA 90095, USA., Ardehali R; Division of Cardiology, Department of Internal Medicine, David Geffen School of Medicine, University of California, Los Angeles, CA 90095, USA; Eli and Edythe Broad Stem Cell Research Center, University of California, Los Angeles, CA 90095, USA; Molecular Biology Institute, University of California, Los Angeles, Los Angeles, CA 90095, USA., Li S; Department of Bioengineering, University of California, Los Angeles, CA 90095, USA; Eli and Edythe Broad Stem Cell Research Center, University of California, Los Angeles, CA 90095, USA; Department of Medicine, David Geffen School of Medicine, University of California, Los Angeles, CA 90095, USA. Electronic address: songli@ucla.edu.
المصدر: Advanced drug delivery reviews [Adv Drug Deliv Rev] 2022 May; Vol. 184, pp. 114233. Date of Electronic Publication: 2022 Mar 15.
نوع المنشور: Journal Article; Review; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Elsevier Science Publishers, B.V Country of Publication: Netherlands NLM ID: 8710523 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1872-8294 (Electronic) Linking ISSN: 0169409X NLM ISO Abbreviation: Adv Drug Deliv Rev Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Amsterdam : Elsevier Science Publishers, B.V., c1987-
مواضيع طبية MeSH: Macrophages* , Wound Healing*, Biocompatible Materials ; Humans ; Immunity
مستخلص: Immune cells have emerged as powerful regulators of regenerative as well as pathological processes. The vast majority of regenerative immunoengineering efforts have focused on macrophages; however, growing evidence suggests that other cells of both the innate and adaptive immune system are as important for successful revascularization and tissue repair. Moreover, spatiotemporal regulation of immune cells and their signaling have a significant impact on the regeneration speed and the extent of functional recovery. In this review, we summarize the contribution of different types of immune cells to the healing process and discuss ways to manipulate and control immune cells in favor of vascularization and tissue regeneration. In addition to cell delivery and cell-free therapies using extracellular vesicles, we discuss in situ strategies and engineering approaches to attract specific types of immune cells and modulate their phenotypes. This field is making advances to uncover the extraordinary potential of immune cells and their secretome in the regulation of vascularization and tissue remodeling. Understanding the principles of immunoregulation will help us design advanced immunoengineering platforms to harness their power for tissue regeneration.
Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
(Copyright © 2022 Elsevier B.V. All rights reserved.)
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معلومات مُعتمدة: R01 CA234343 United States CA NCI NIH HHS; R01 HL148714 United States HL NHLBI NIH HHS; R01 DK112939 United States DK NIDDK NIH HHS; R01 HL149940 United States HL NHLBI NIH HHS; R56 DE029157 United States DE NIDCR NIH HHS
فهرسة مساهمة: Keywords: Biomaterial; Cell delivery; Extracellular vesicles; Immune cell metabolism; Immunomodulation; Macrophages; Neutrophils; Patterning; Stiffness; T cells
المشرفين على المادة: 0 (Biocompatible Materials)
تواريخ الأحداث: Date Created: 20220319 Date Completed: 20220426 Latest Revision: 20231219
رمز التحديث: 20231219
مُعرف محوري في PubMed: PMC10726003
DOI: 10.1016/j.addr.2022.114233
PMID: 35304171
قاعدة البيانات: MEDLINE
الوصف
تدمد:1872-8294
DOI:10.1016/j.addr.2022.114233