Abstract

Tenascin-C plays important roles in immunity. Toll-like receptor 4, integrin α9β1 and chemokines have already been identified as key players in executing the immune regulatory functions of tenascin-C. Tenascin-C is also found in reticular fibers in lymphoid tissues, which are major sites involved in the regulation of adaptive immunity. Did the “tool box” for reading and interpreting the immune-regulating instructions imposed by tenascins and tenascin-C co-evolve? Though the extracellular matrix is ancient, tenascins evolved relatively recently. Tenascin-like genes are first encountered in cephalochordates and urochordates, which are widely accepted as the early branching chordate lineages. Vertebrates lacking jaws like the lamprey have tenascins, but a tenascin gene that clusters in the tenascin-C clade first appears in cartilaginous fish. Adaptive immunity apparently evolved independently in jawless and jawed vertebrates, with the former using variable lymphocyte receptors for antigen recognition, and the latter using immunoglobulins. Thus, while tenascins predate the appearance of adaptive immunity, the first tenascin-C appears to have evolved in the first organisms with immunoglobulin-based adaptive immunity. While a C-X-C chemokine is present in the lamprey, C-C chemokines also appear in the first organisms with immunoglobulin-based adaptive immunity, as does the major histocompatibility complex, T-cell receptors, Toll-like receptor 4 and integrin α9β1. Given the importance of tenascin-C in inflammatory events, the co-evolution of tenascin-C and key elements of adaptive and innate immunity is suggestive of a fundamental role for this extracellular matrix glycoprotein in the immune response of jawed vertebrates.

Highlights

  • Tenascins are extracellular matrix glycoproteins with one or more epidermal growth factor-like repeats, multiple fibronectin type III (FNIII) domains, and a C-terminal fibrinogen-related domain (FReD) [1]

  • Tenascins appeared with the first chordates, but tenascin-C evolved with the jawed vertebrates

  • This coincides with the evolution of immunoglobulin-based adaptive immunity, the major histocompatibility complex (MHC), most chemokines, T-cell receptors, interferon Types I and II [43], and TLR-4 (Figure 1)

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Summary

Introduction

Tenascins are extracellular matrix glycoproteins with one or more epidermal growth factor-like repeats, multiple fibronectin type III (FNIII) domains, and a C-terminal fibrinogen-related domain (FReD) [1]. In this mini review we will explore the possibility that tenascin-C appeared during evolution along with other critical players in the immune system, pointing to fundamental roles for this extracellular matrix glycoprotein in regulating inflammatory events. Tenascin-C and tenascin-R evolved together with the first jawed vertebrates (gnathostomes), and additional members of the family appeared later during evolution.

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