A review of the osteoderms of lizards (Reptilia: Squamata).

Squamata armour dermal skeleton development evolution function lizard osteoderms

Journal

Biological reviews of the Cambridge Philosophical Society
ISSN: 1469-185X
Titre abrégé: Biol Rev Camb Philos Soc
Pays: England
ID NLM: 0414576

Informations de publication

Date de publication:
02 2022
Historique:
revised: 30 07 2021
received: 28 12 2020
accepted: 03 08 2021
pubmed: 17 8 2021
medline: 24 3 2022
entrez: 16 8 2021
Statut: ppublish

Résumé

Osteoderms are mineralised structures consisting mainly of calcium phosphate and collagen. They form directly within the skin, with or without physical contact with the skeleton. Osteoderms, in some form, may be primitive for tetrapods as a whole, and are found in representatives of most major living lineages including turtles, crocodilians, lizards, armadillos, and some frogs, as well as extinct taxa ranging from early tetrapods to dinosaurs. However, their distribution in time and space raises questions about their evolution and homology in individual groups. Among lizards and their relatives, osteoderms may be completely absent; present only on the head or dorsum; or present all over the body in one of several arrangements, including non-overlapping mineralised clusters, a continuous covering of overlapping plates, or as spicular mineralisations that thicken with age. This diversity makes lizards an excellent focal group in which to study osteoderm structure, function, development and evolution. In the past, the focus of researchers was primarily on the histological structure and/or the gross anatomy of individual osteoderms in a limited sample of taxa. Those studies demonstrated that lizard osteoderms are sometimes two-layered structures, with a vitreous, avascular layer just below the epidermis and a deeper internal layer with abundant collagen within the deep dermis. However, there is considerable variation on this model, in terms of the arrangement of collagen fibres, presence of extra tissues, and/or a cancellous bone core bordered by cortices. Moreover, there is a lack of consensus on the contribution, if any, of osteoblasts in osteoderm development, despite research describing patterns of resorption and replacement that would suggest both osteoclast and osteoblast involvement. Key to this is information on development, but our understanding of the genetic and skeletogenic processes involved in osteoderm development and patterning remains minimal. The most common proposition for the presence of osteoderms is that they provide a protective armour. However, the large morphological and distributional diversity in lizard osteoderms raises the possibility that they may have other roles such as biomechanical reinforcement in response to ecological or functional constraints. If lizard osteoderms are primarily for defence, whether against predators or conspecifics, then this 'bony armour' might be predicted to have different structural and/or mechanical properties compared to other hard tissues (generally intended for support and locomotion). The cellular and biomineralisation mechanisms by which osteoderms are formed could also be different from those of other hard tissues, as reflected in their material composition and nanostructure. Material properties, especially the combination of malleability and resistance to impact, are of interest to the biomimetics and bioinspired material communities in the development of protective clothing and body armour. Currently, the literature on osteoderms is patchy and is distributed across a wide range of journals. Herein we present a synthesis of current knowledge on lizard osteoderm evolution and distribution, micro- and macrostructure, development, and function, with a view to stimulating further work.

Identifiants

pubmed: 34397141
doi: 10.1111/brv.12788
pmc: PMC9292694
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-19

Informations de copyright

© 2021 The Authors. Biological Reviews published by John Wiley & Sons Ltd on behalf of Cambridge Philosophical Society.

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Auteurs

Catherine Williams (C)

Department of Biomedical Sciences, University of Guelph, 50 Stone Road East, Guelph, ON, N1G 2W1, Canada.
Department of Biology, Aarhus University, Ny Munkegade 114-116, Aarhus C, DK-8000, Denmark.

Alexander Kirby (A)

Department of Medical Physics and Biomedical Engineering, University College London, London, WC1E 6BT, U.K.
Department of Cell and Developmental Biology, University College London, London, WC1E 6BT, U.K.

Arsalan Marghoub (A)

Department of Mechanical Engineering, University College London, London, WC1E 7JE, U.K.

Loïc Kéver (L)

Département Adaptations du Vivant, UMR 7179 MECADEV C.N.R.S/M.N.H.N., Bâtiment d'Anatomie Comparée, 55 rue Buffon, Paris, 75005, France.

Sonya Ostashevskaya-Gohstand (S)

Department of Life Sciences, Faculty of Natural Sciences, Imperial College London, Silwood Park Campus, Berkshire, SL5 7PY, U.K.

Sergio Bertazzo (S)

Department of Medical Physics and Biomedical Engineering, University College London, London, WC1E 6BT, U.K.

Mehran Moazen (M)

Department of Mechanical Engineering, University College London, London, WC1E 7JE, U.K.

Arkhat Abzhanov (A)

Department of Life Sciences, Faculty of Natural Sciences, Imperial College London, Silwood Park Campus, Berkshire, SL5 7PY, U.K.

Anthony Herrel (A)

Département Adaptations du Vivant, UMR 7179 MECADEV C.N.R.S/M.N.H.N., Bâtiment d'Anatomie Comparée, 55 rue Buffon, Paris, 75005, France.

Susan E Evans (SE)

Department of Cell and Developmental Biology, University College London, London, WC1E 6BT, U.K.

Matt Vickaryous (M)

Department of Biomedical Sciences, University of Guelph, 50 Stone Road East, Guelph, ON, N1G 2W1, Canada.

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