Proceed with Caution: Mouse Deep Digit Flexor Tendon Injury Model

Background:. The purpose of this study was to determine the feasibility of using mouse models for translational study of flexor tendon repair and reconstruction. Methods:. Quantitative data detailing the gross anatomy, biomechanical characteristics, and microscopic structure of the deep digit flexor...

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Main Authors: Ashley L. Titan, MD, Evan Fahy, MD, Kellen Chen, PhD, Deshka S. Foster, MD, Ross Bennett-Kennett, BS, Reinhold H. Dauskardt, PhD, Geoffrey C. Gurtner, MD, James Chang, MD, Paige M. Fox, MD, PhD, Michael T. Longaker, MD, MBA, DSc (hon), FACS
Format: Article
Language:English
Published: Wolters Kluwer 2021-01-01
Series:Plastic and Reconstructive Surgery, Global Open
Online Access:http://journals.lww.com/prsgo/fulltext/10.1097/GOX.0000000000003359
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spelling doaj-f48efa34d93e4f2ab4aefcd428e430652021-02-26T03:25:48ZengWolters KluwerPlastic and Reconstructive Surgery, Global Open2169-75742021-01-0191e335910.1097/GOX.0000000000003359202101000-00021Proceed with Caution: Mouse Deep Digit Flexor Tendon Injury ModelAshley L. Titan, MD0Evan Fahy, MD1Kellen Chen, PhD2Deshka S. Foster, MD3Ross Bennett-Kennett, BS4Reinhold H. Dauskardt, PhD5Geoffrey C. Gurtner, MD6James Chang, MD7Paige M. Fox, MD, PhD8Michael T. Longaker, MD, MBA, DSc (hon), FACS9From the * Department of Surgery, Division of Plastic and Reconstructive Surgery, Stanford University School of Medicine, Palo Alto, Calif.† Hagey Laboratory for Pediatric Regenerative Medicine, Department of Surgery, Division of Plastic and Reconstructive Surgery, Stanford University School of Medicine, Palo Alto, Calif.† Hagey Laboratory for Pediatric Regenerative Medicine, Department of Surgery, Division of Plastic and Reconstructive Surgery, Stanford University School of Medicine, Palo Alto, Calif.From the * Department of Surgery, Division of Plastic and Reconstructive Surgery, Stanford University School of Medicine, Palo Alto, Calif.‡ Department of Materials Science and Engineering, Stanford University, Palo Alto, Calif.‡ Department of Materials Science and Engineering, Stanford University, Palo Alto, Calif.From the * Department of Surgery, Division of Plastic and Reconstructive Surgery, Stanford University School of Medicine, Palo Alto, Calif.From the * Department of Surgery, Division of Plastic and Reconstructive Surgery, Stanford University School of Medicine, Palo Alto, Calif.From the * Department of Surgery, Division of Plastic and Reconstructive Surgery, Stanford University School of Medicine, Palo Alto, Calif.From the * Department of Surgery, Division of Plastic and Reconstructive Surgery, Stanford University School of Medicine, Palo Alto, Calif.Background:. The purpose of this study was to determine the feasibility of using mouse models for translational study of flexor tendon repair and reconstruction. Methods:. Quantitative data detailing the gross anatomy, biomechanical characteristics, and microscopic structure of the deep digit flexor tendon (DDF) of the mouse hindpaw were obtained. Histological characterization of the DDF and the anatomy of the digit in the mouse hindpaw are detailed. Biomechanical testing determined the load-to-failure, stress, elastic modulus, and the site of tendon failure. Results:. In gross anatomy, the origins and insertions of the mouse deep digit flexor tendon are similar to those of the human digit, surrounded by a synovial sheath that is only 1- to 2-cells thick. A neurovascular network runs on each side of the digit outside the synovial sheath, but does not clearly penetrate it. The thickness of the DDF is 0.14 ± 0.03 mm and the width is 0.3 ± 0.03 mm. The thickness of the DDF is less than that of 9-0 nylon needle. The mean failure force of the deep flexor tendon was 2.79 ± 0.53N. Conclusions:. The gross anatomy of the mouse hindpaw digit is similar to that of the human digit except for key differences seen in the synovial sheath and vascular supply. The dimensions of the mouse DDF make it challenging to create a clinically translatable repair model using currently available surgical techniques. Despite the similarities between the human and mouse anatomy, and the powerful basic science tools available in murine models, mice are an unreliable model for assessing flexor tendon injury and repair.http://journals.lww.com/prsgo/fulltext/10.1097/GOX.0000000000003359
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language English
format Article
sources DOAJ
author Ashley L. Titan, MD
Evan Fahy, MD
Kellen Chen, PhD
Deshka S. Foster, MD
Ross Bennett-Kennett, BS
Reinhold H. Dauskardt, PhD
Geoffrey C. Gurtner, MD
James Chang, MD
Paige M. Fox, MD, PhD
Michael T. Longaker, MD, MBA, DSc (hon), FACS
spellingShingle Ashley L. Titan, MD
Evan Fahy, MD
Kellen Chen, PhD
Deshka S. Foster, MD
Ross Bennett-Kennett, BS
Reinhold H. Dauskardt, PhD
Geoffrey C. Gurtner, MD
James Chang, MD
Paige M. Fox, MD, PhD
Michael T. Longaker, MD, MBA, DSc (hon), FACS
Proceed with Caution: Mouse Deep Digit Flexor Tendon Injury Model
Plastic and Reconstructive Surgery, Global Open
author_facet Ashley L. Titan, MD
Evan Fahy, MD
Kellen Chen, PhD
Deshka S. Foster, MD
Ross Bennett-Kennett, BS
Reinhold H. Dauskardt, PhD
Geoffrey C. Gurtner, MD
James Chang, MD
Paige M. Fox, MD, PhD
Michael T. Longaker, MD, MBA, DSc (hon), FACS
author_sort Ashley L. Titan, MD
title Proceed with Caution: Mouse Deep Digit Flexor Tendon Injury Model
title_short Proceed with Caution: Mouse Deep Digit Flexor Tendon Injury Model
title_full Proceed with Caution: Mouse Deep Digit Flexor Tendon Injury Model
title_fullStr Proceed with Caution: Mouse Deep Digit Flexor Tendon Injury Model
title_full_unstemmed Proceed with Caution: Mouse Deep Digit Flexor Tendon Injury Model
title_sort proceed with caution: mouse deep digit flexor tendon injury model
publisher Wolters Kluwer
series Plastic and Reconstructive Surgery, Global Open
issn 2169-7574
publishDate 2021-01-01
description Background:. The purpose of this study was to determine the feasibility of using mouse models for translational study of flexor tendon repair and reconstruction. Methods:. Quantitative data detailing the gross anatomy, biomechanical characteristics, and microscopic structure of the deep digit flexor tendon (DDF) of the mouse hindpaw were obtained. Histological characterization of the DDF and the anatomy of the digit in the mouse hindpaw are detailed. Biomechanical testing determined the load-to-failure, stress, elastic modulus, and the site of tendon failure. Results:. In gross anatomy, the origins and insertions of the mouse deep digit flexor tendon are similar to those of the human digit, surrounded by a synovial sheath that is only 1- to 2-cells thick. A neurovascular network runs on each side of the digit outside the synovial sheath, but does not clearly penetrate it. The thickness of the DDF is 0.14 ± 0.03 mm and the width is 0.3 ± 0.03 mm. The thickness of the DDF is less than that of 9-0 nylon needle. The mean failure force of the deep flexor tendon was 2.79 ± 0.53N. Conclusions:. The gross anatomy of the mouse hindpaw digit is similar to that of the human digit except for key differences seen in the synovial sheath and vascular supply. The dimensions of the mouse DDF make it challenging to create a clinically translatable repair model using currently available surgical techniques. Despite the similarities between the human and mouse anatomy, and the powerful basic science tools available in murine models, mice are an unreliable model for assessing flexor tendon injury and repair.
url http://journals.lww.com/prsgo/fulltext/10.1097/GOX.0000000000003359
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