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Equine veterinary journal2004; 36(3); 236-241; doi: 10.2746/0425164044877198

Epidermal cell proliferation in the equine hoof wall.

Abstract: Current theories explaining how the hoof wall 'grows' and moves past the stationary distal phalanx are speculative and based on incomplete evidence. Movement in the lamellar region could occur by cell proliferation or an enzyme-based remodelling process. Since laminitis pathogenesis appears to involve increased transcription and activation of enzymes normally involved in tissue remodelling, it is important to know precisely which process dominates the lamellar region of the hoof.. Objective: To investigate epidermal cell proliferation in the equine hoof wall and calculate a proliferative index (PI) for the coronet, lamellae and toe. Methods: An analogue of thymidine, 5-bromo-2'-deoxyuridine (BRdU), was infused i.v. into 5 ponies. After tissue harvesting, BRdU (and therefore basal cell proliferation) was detected immunohistochemically using mouse anti-BRdU. PIs were calculated for the coronet and 10 levels of the dorsal hoof wall lamellae. Results: The highest PIs (mean +/- s.e.) were in the coronet; 12.04% +/- 1.59 and proximal lamellae (7.13% +/- 1.92) and are therefore growth zones of the proximal hoof wall. PIs of more distal lamellae were 0.11% +/- 0.04 to 0.97% +/- 0.29; significantly lower (P = 0.05) than the lamellar growth zone. Conclusions: A 20-fold PI decrease between proximal and more distal lamellae suggests that the majority of the normal lamellae are nonproliferative and their main function is to suspend the distal phalanx within the hoof capsule. Remodelling within the hoof wall epidermal lamellae, which must occur as the hoof wall moves past the stationary distal phalanx, is a process not requiring epidermal cell proliferation. Conclusions: A hoof lamellar epidermis that remodels using the same MMPs involved in laminitis pathogenesis implies that laminitis is a normal process out of control. Understanding MMP control and how the normal lamellar epidermis achieves this will help in the development of better laminitis preventative and treatment strategies.
Publication Date: 2004-05-19 PubMed ID: 15147131DOI: 10.2746/0425164044877198Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research article investigates the process of cell proliferation in the lamellar region of an equine hoof wall. The findings reveal that proximal layers of the hoof wall have higher cell proliferation, and the distal lamellae majorly function to hold the distal phalanx within the hoof capsule.

Objective of the Study

  • The major aim of the study was to delve deeper into the process of cell proliferation in the lamellar region of an equine hoof wall, particularly focusing on the epidermal cells. They sought to calculate a proliferative index (PI) for different parts of the hoof (coronet, lamellae, and toe).

Research Methodology

  • An analogue of thymidine, known as 5-bromo-2′-deoxyuridine (BRdU), was infused into five ponies and was then detected through immunohistochemical means using mouse anti-BRdU.
  • The PIs were calculated for the coronet and ten levels of the dorsal hoof wall lamellae.

Key Findings

  • The results showed that the highest PIs were in the proximal lamellae (7.13% +/- 1.92) and the coronet (12.04% +/- 1.59), which indicates that these are the main areas of growth in the proximal hoof wall.
  • The PIs of the more distal lamellae were significantly lower, suggesting the majority of the normal lamellae are nonproliferative and primarily function to suspend the distal phalanx within the hoof capsule.
  • The huge decrease in PI from proximal to distal lamellae indicates that remodelling within the hoof wall epidermal lamellae does not require cell proliferation. This process happens as the hoof wall moves past the stationary distal phalanx.

Conclusions and Implications

  • The study concludes that the majority of normal lamellae do not proliferate and mainly function to hold the distal phalanx within the hoof capsule. Therefore, remodelling within the hoof wall epidermal lamellae does not require cell proliferation.
  • The hoof lamellar epidermis, which remodels using the same MMPs (metalloproteinases) involved in the pathogenesis of laminitis, implies that laminitis is a normal process that has escalated beyond control.
  • Understanding how the normal lamellar epidermis controls MMP and achieving more research on this will be instrumental in developing better strategies for preventing and treating laminitis.

Cite This Article

APA
Daradka M, Pollitt CC. (2004). Epidermal cell proliferation in the equine hoof wall. Equine Vet J, 36(3), 236-241. https://doi.org/10.2746/0425164044877198

Publication

ISSN: 0425-1644
NlmUniqueID: 0173320
Country: United States
Language: English
Volume: 36
Issue: 3
Pages: 236-241

Researcher Affiliations

Daradka, M
  • Australian Equine Laminitis Research Unit, School of Veterinary Science, Faculty of Natural Resources Agriculture and Veterinary Science, The University of Queensland, Brisbane, Queensland 4072, Australia.
Pollitt, C C

    MeSH Terms

    • Animals
    • Basement Membrane / cytology
    • Basement Membrane / growth & development
    • Basement Membrane / metabolism
    • Bromodeoxyuridine / administration & dosage
    • Cell Division
    • Epidermal Cells
    • Epidermis / growth & development
    • Epidermis / metabolism
    • Female
    • Foot Diseases / enzymology
    • Foot Diseases / etiology
    • Foot Diseases / pathology
    • Foot Diseases / veterinary
    • Hoof and Claw / cytology
    • Hoof and Claw / growth & development
    • Hoof and Claw / metabolism
    • Horse Diseases / enzymology
    • Horse Diseases / etiology
    • Horse Diseases / pathology
    • Horses
    • Immunohistochemistry / veterinary
    • Inflammation / enzymology
    • Inflammation / etiology
    • Inflammation / pathology
    • Inflammation / veterinary
    • Infusions, Intravenous / veterinary
    • Male
    • Metalloendopeptidases / metabolism

    Citations

    This article has been cited 7 times.
    1. Dadone L, Foxworth S, Goedhals J, Han S, Bapodra-Villaverde P, Yap SW, Radile T, Deacon F. Anatomy and baseline histology of the hoof capsule, corium, and digital cushion in free-ranging southern giraffe (Giraffa giraffa). PLoS One 2025;20(12):e0339972.
      doi: 10.1371/journal.pone.0339972pubmed: 41468417google scholar: lookup
    2. Hobbs SJ, Curtis S, Martin J, Sinclair J, Clayton HM. Hoof Matters: Developing an Athletic Thoroughbred Hoof. Animals (Basel) 2022 Nov 11;12(22).
      doi: 10.3390/ani12223119pubmed: 36428348google scholar: lookup
    3. Vercelli C, Tursi M, Miretti S, Giusto G, Gandini M, Re G, Valle E. Effect of sugar metabolite methylglyoxal on equine lamellar explants: An ex vivo model of laminitis. PLoS One 2021;16(7):e0253840.
      doi: 10.1371/journal.pone.0253840pubmed: 34314429google scholar: lookup
    4. Armstrong C, Cassimeris L, Da Silva Santos C, Micoogullari Y, Wagner B, Babasyan S, Brooks S, Galantino-Homer H. The expression of equine keratins K42 and K124 is restricted to the hoof epidermal lamellae of Equus caballus. PLoS One 2019;14(9):e0219234.
      doi: 10.1371/journal.pone.0219234pubmed: 31550264google scholar: lookup
    5. Yang Q, Pinto VMR, Duan W, Paxton EE, Dessauer JH, Ryan W, Lopez MJ. In vitro Characteristics of Heterogeneous Equine Hoof Progenitor Cell Isolates. Front Bioeng Biotechnol 2019;7:155.
      doi: 10.3389/fbioe.2019.00155pubmed: 31355191google scholar: lookup
    6. Cassimeris L, Engiles JB, Galantino-Homer H. Detection of endoplasmic reticulum stress and the unfolded protein response in naturally-occurring endocrinopathic equine laminitis. BMC Vet Res 2019 Jan 10;15(1):24.
      doi: 10.1186/s12917-018-1748-xpubmed: 30630474google scholar: lookup
    7. Baskerville CL, Chockalingham S, Harris PA, Bailey SR. The effect of insulin on equine lamellar basal epithelial cells mediated by the insulin-like growth factor-1 receptor. PeerJ 2018;6:e5945.
      doi: 10.7717/peerj.5945pubmed: 30519508google scholar: lookup