Literature DB >> 30118577

Adipose-derived stem cells and the stromal vascular fraction in polyglycolic acid-collagen nerve conduits promote rat facial nerve regeneration.

Mari Shimizu1, Hajime Matsumine1, Hironobu Osaki2, Yoshifumi Ueta2, Satoshi Tsunoda1, Wataru Kamei1, Kazuki Hashimoto1, Yosuke Niimi1, Yorikatsu Watanabe3, Mariko Miyata2, Hiroyuki Sakurai1.   

Abstract

Adipose-derived stem cells (ADSCs) and the stromal vascular fraction (SVF) promote nerve regeneration. Biodegradable nerve conduits are used to treat peripheral nerve injuries, but their efficiencies are lower than those of autologous nerve grafts. This study developed biodegradable nerve conduits containing ADSCs and SVF and evaluated their facial nerve regenerating abilities in a rat model with a 7-mm nerve defect. SVF and ADSCs were individually poured into nerve conduits with polyglycolic acid-type I collagen as a scaffold (ADSCs and SVF groups). The conduits were grafted on to the nerve defects. As the control, the defect was bridged with polyglycolic acid-collagen nerve conduits without cells. At 13 weeks, after transplantation, the regenerated nerves were evaluated physiologically and histologically. The compound muscle action potential of the SVF group was significantly higher in amplitude than that of the control group. Electron microscopy showed that the axon diameter of the SVF group was the largest, followed by the ADSC group and control group with significant differences among them. The SVF group had the largest fiber diameter, followed by the ADSC group and control group with significant differences among them. The ADSC group had the highest myelin thickness, followed by the SVF group and control group with significant differences among them. Identical excellent promoting effects on nerve regeneration were observed in both the ADSC and SVF groups. Using SVF in conduits was more practical than using ADSCs because only the enzymatic process was required to prepare SVF, indicating that SVF could be more suitable to induce nerve regeneration.
© 2018 by the Wound Healing Society.

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Year:  2018        PMID: 30118577     DOI: 10.1111/wrr.12665

Source DB:  PubMed          Journal:  Wound Repair Regen        ISSN: 1067-1927            Impact factor:   3.617


  19 in total

Review 1.  Advances and clinical challenges for translating nerve conduit technology from bench to bed side for peripheral nerve repair.

Authors:  Poonam Meena; Anupama Kakkar; Mukesh Kumar; Nitin Khatri; Rakesh Kumar Nagar; Aarti Singh; Poonam Malhotra; Manish Shukla; Sumit Kumar Saraswat; Supriya Srivastava; Rajan Datt; Siddharth Pandey
Journal:  Cell Tissue Res       Date:  2020-11-17       Impact factor: 5.249

2.  [Effect of the local application of stem cells on repairing facial nerve defects: a systematic review].

Authors:  Dan Zhao; Yue-Heng Li; Zheng-Yan Yang; Ting Cai; Xiao-Yan Wu; Yu Xia; Zhi Zhou
Journal:  Hua Xi Kou Qiang Yi Xue Za Zhi       Date:  2020-02-01

3.  Corrigendum to "Dedifferentiated fat cells in polyglycolic acid-collagen nerve conduits promote rat facial nerve regeneration" [Regen Ther 11 (2019) 240-248].

Authors:  Hiroshi Fujimaki; Hajime Matsumine; Hironobu Osaki; Yoshifumi Ueta; Wataru Kamei; Mari Shimizu; Kazuki Hashimoto; Kaori Fujii; Tomohiko Kazama; Taro Matsumoto; Yosuke Niimi; Mariko Miyata; Hiroyuki Sakurai
Journal:  Regen Ther       Date:  2020-06-10       Impact factor: 3.419

4.  Secondary release of the peripheral nerve with autologous fat derivates benefits for functional and sensory recovery.

Authors:  Natalia E Krzesniak; Anna Sarnowska; Anna Figiel-Dabrowska; Katarzyna Osiak; Krystyna Domanska-Janik; Bartłomiej H Noszczyk
Journal:  Neural Regen Res       Date:  2021-05       Impact factor: 5.135

Review 5.  Facial Nerve Repair: Bioengineering Approaches in Preclinical Models.

Authors:  Fuat Baris Bengur; Conrad Stoy; Mary A Binko; Wayne Vincent Nerone; Caroline Nadia Fedor; Mario G Solari; Kacey G Marra
Journal:  Tissue Eng Part B Rev       Date:  2021-04-13       Impact factor: 7.376

6.  Hyaluronic Acid (HA) Receptors and the Motility of Schwann Cell(-Like) Phenotypes.

Authors:  Sihem Ouasti; Alessandro Faroni; Paul J Kingham; Matilde Ghibaudi; Adam J Reid; Nicola Tirelli
Journal:  Cells       Date:  2020-06-17       Impact factor: 6.600

7.  PDGF enhances the protective effect of adipose stem cell-derived extracellular vesicles in a model of acute hindlimb ischemia.

Authors:  Tatiana Lopatina; Enrica Favaro; Cristina Grange; Massimo Cedrino; Andrea Ranghino; Sergio Occhipinti; Sofia Fallo; Fabrizio Buffolo; Daria A Gaykalova; Maria M Zanone; Renato Romagnoli; Giovanni Camussi
Journal:  Sci Rep       Date:  2018-12-04       Impact factor: 4.379

8.  Dedifferentiated fat cells in polyglycolic acid-collagen nerve conduits promote rat facial nerve regeneration.

Authors:  Hiroshi Fujimaki; Hajime Matsumine; Hironobu Osaki; Yoshifumi Ueta; Wataru Kamei; Mari Shimizu; Kazuki Hashimoto; Kaori Fujii; Tomohiko Kazama; Taro Matsumoto; Yosuke Niimi; Mariko Miyata; Hiroyuki Sakurai
Journal:  Regen Ther       Date:  2019-09-12       Impact factor: 3.419

9.  Surgical anatomy of the ovine sural nerve for facial nerve regeneration and reconstruction research.

Authors:  Yosuke Niimi; Satoshi Fukuda; Ryan S Gilbert; Tuvshintugs Baljinnyam; Yu Niimi; Hajime Matsumine; Keibun Liu; Sam Jacob; Hal K Hawkins; Robert A Cox; David N Herndon; Donald S Prough; Perenlei Enkhbaatar
Journal:  Sci Rep       Date:  2019-07-22       Impact factor: 4.379

Review 10.  Potential Therapeutic Strategies and Substances for Facial Nerve Regeneration Based on Preclinical Studies.

Authors:  Myung Chul Yoo; Jinmann Chon; Junyang Jung; Sung Su Kim; Seonhwan Bae; Sang Hoon Kim; Seung Geun Yeo
Journal:  Int J Mol Sci       Date:  2021-05-06       Impact factor: 5.923

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