Method Article

Adult Mouse Digit Amputation and Regeneration: A Simple Model to Investigate Mammalian Blastema Formation and Intramembranous Ossification

DOI:

10.3791/59749

July 12th, 2019

In This Article

Summary

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Here, we present a protocol of adult mouse terminal phalanx amputation to investigate mammalian blastema formation and intramembranous ossification, analyzed by fluorescent immunohistochemistry and sequential in-vivo microcomputed tomography.

Abstract

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Here, we present a protocol of adult mouse distal terminal phalanx (P3) amputation, a procedurally simple and reproducible mammalian model of epimorphic regeneration, which involves blastema formation and intramembranous ossification analyzed by fluorescence immunohistochemistry and sequential in-vivo microcomputed tomography (μCT). Mammalian regeneration is restricted to amputations transecting the distal region of the terminal phalanx (P3); digits amputated at more proximal levels fail to regenerate and undergo fibrotic healing and scar formation. The regeneration response is mediated by the formation of a proliferative blastema, followed by bone regeneration via intramembranous ossification to restore the amputated skeletal length. P3 amputation is a preclinical model to investigate epimorphic regeneration in mammals, and is a powerful tool for the design of therapeutic strategies to replace fibrotic healing with a successful regenerative response. Our protocol uses fluorescence immunohistochemistry to 1) identify early-and-late blastema cell populations, 2) study revascularization in the context of regeneration, and 3) investigate intramembranous ossification without the need for complex bone stabilization devices. We also demonstrate the use of sequential in vivo μCT to create high resolution images to examine morphological changes after amputation, as well as quantify volume and length changes in the same digit over the course of regeneration. We believe this protocol offers tremendous utility to investigate both epimorphic and tissue regenerative responses in mammals.

Introduction

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Mammals, including humans and mice, have the capacity to regenerate the tips of their digits after distal amputation of the terminal phalanx (P3)1,2,3. In mice, the regeneration response is amputation-level-dependent; increasingly proximal digit amputations display a progressively attenuated regenerative response until complete regenerative failure at amputations transecting and proximal to the P3 nail matrix4,5,6,7,8

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Protocol

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All animal use and techniques were in compliance with the standard operating procedures of the Institutional Animal Care and Use Committee of Texas A&M University.

1. Adult Mouse Hind Limb Distal P3 Amputation

  1. Anesthetize an 8 to 12 week-old CD-1 mouse (Table of Materials) using isoflurane gas in oxygen; initially anesthetize at 3% in a chamber, followed by 2% isoflurane supplied by a nosecone over the duration of the surgery. Apply ophthalmic ointment on eyes to prevent dryness while under anesthesia.
    NOTE: The adult P3 amputation studies standardized in our lab are performed on 8 to....

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Results

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Adult mouse regenerating P3 digits at 6/7 DPA (Figure 2A-D), 9 DPA (Figure 2E-H), and 10 DPA (Figure 2I-L) were immunostained with antibodies to Runx2, OSX, and PCNA to visualize intramembranous bone regeneration, and immunostained with antibodies to CXCR4 and vWF to visualize blastema formation. Representative μCT renderings of digits scanned prior to amputation and at various time.......

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Discussion

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This protocol describes a standardized procedure of adult mouse distal P3 amputation, fluorescent immunohistochemical staining to visualize and investigate blastema formation and intramembranous ossification, and sequential in-vivo µCT scanning to identify bone morphological, volume, and length changes post amputation. P3 amputation is a unique, procedurally simple, and reproducible model to analyze a pro-regenerative wound environment that triggers blastema formation. Furthermore, the P3 digit model offers numerous.......

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Disclosures

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The authors have nothing to disclose.

Acknowledgements

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We thank members of the Muneoka Lab and the Texas Institute for Genomic Medicine (TIGM). This work was supported by Texas A&M University.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Protein Block Serum FreeDAKOX0909Ready to use
Mouse anti-PCNA antibodyAbcamab291:2000 dilution
Rat anti-CXCR4 antibodyR&D SystemsMAB216511:500 dilution
Rabbit anti-human vWF XIII antibodyDAKOA00821:800 dilution
Rabbit anti-osterix, SP7 antibodyAbcamab225521:400 dilution
Rabbit anti-Runx2 antibodySigma-Aldrich Co.HPA0220401:250 dilution
Alexa Fluor 647-conjugated goat anti-mouse IgG (H+L)InvitrogenA212351:500 dilution
Alexa Fluor 488-conjugated goat anti-rabbit IgG (H+L)InvitrogenA110081:500 dilution
Alexa Fluor 568-conjugated goat anti-rat IgG (H+L)InvitrogenA110771:500 dilution
Prolong Gold antifade reagentInvitrogenP36930Ready to use
Surgipath Decalicifier 1Leica Biosystems3800400Ready to use
Z-Fix, Aqueous buffered zinc formalin fixativeAnatech LTD174Ready to use
CD-1 Female MouseEnvigoICR(CD-1)8-12-weeks-old
vivaCT 40SCANCO Medical

References

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  1. Douglas, B. S. Conservative management of guillotine amputation of the finger in children. Australian Paediatric Journal. 8, 86-89 (1972).
  2. Illingworth, C. M. Trapped fingers and amputated finger tips in children. Journal of Pediatric Surgery. <....

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Tags

Mouse Digit AmputationBlastema FormationIntramembranous OssificationFluorescence ImmunohistochemistryMicrocomputed TomographyEpimorphic RegenerationTerminal PhalanxBone RegenerationVascularization AnalysisSequential Imaging

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