Encyclopedia of Signaling Molecules

2018 Edition
| Editors: Sangdun Choi

Intercellular Adhesion Molecule-5

Reference work entry
DOI: https://doi.org/10.1007/978-3-319-67199-4_101656

Synonyms

Historical Background

The discovery of ICAM-5 was made by K. Mori and colleagues in 1987. Mice were immunized with the synaptic fractions of olfactory bulb neurons and a series of monoclonal antibodies was generated. One of the antibodies showed immunoreactivity exclusively with the telencephalon (Mori et al. 1987). The target molecule was named telencephalin. Further analysis with this antibody showed a somatodendritic distribution, specific to neuronal membranes. The expression was found to be developmentally regulated.

By affinity chromatography, telencephalin was characterized as a 500 kDa glycoprotein consisting of four monomers. In subsequent studies, the target cDNA was generated and considerable homology to the intercellular adhesion molecule, ICAM, family found (Yoshihara et al. 1994). Telencephalin was included as the fifth and so far the youngest member of the family. Consistent with the nomenclature, it was renamed ICAM-5 (Gahmberg 1997).

Expression Pattern

In the human genome, the ICAM-5 gene is localized to chromosome 19 (19p13.2) together with the genes of ICAM-1, -3, and -4. ICAM-5 shows a high degree of homology between different mammalian species. None of the other ICAM family members is confined to neurons. ICAM-1 is ubiquitously expressed in the body and it is also found on astrocytes in the brain. The expression of ICAM-5 is initiated around the time of birth and the expression level increases during the postnatal development until it reaches a plateau at around 5 months after birth in humans and persists into adulthood. Interestingly, it is only expressed somatodendritically in excitatory telencephalic neurons (Fig. 1). The subcellular expression pattern is determined by a single amino acid residue, phenylalanine-905 (Mitsui et al. 2005). ICAM-5 is abundant in filopodia and thin spines and less so in the synaptic cleft and the head of mature, mushroom-shaped spines. On the neuronal membrane, it is associated with flotillin, a marker for lipid rafts and its recycling into endosomes is mediated through the small GTPase, ADP-ribosylation factor 6, ARF6 (Raemaekers et al. 2012).
Intercellular Adhesion Molecule-5, Fig. 1

Dissociated primary hippocampal cultures from sibling matched wild-type (A, B, C, D) and ICAM-5 knockout (a, b, c, d) C57Bl/6jOla mice. After 14 days in culture, the cells were fixed with paraformaldehyde and stained by immunofluorescence. (a) and (A) show staining for ICAM-5 (cyan), (b) and (B) show staining for Map 2 (magenta), (c) and (C) show staining for Synapsin (blue), and (d) and (D) are all channels merged and the antigens visualized by their corresponding colors. ICAM-5 localizes to dendrites and thin filopodia. Scale bar: 10 μm

Structure

Like all other members of the ICAM family, ICAM-5 belongs to the immunoglobulin, Ig, superfamily, and it is a type 1 integral protein. The extracellular part of the protein is the most complex in the ICAM-family with nine Ig domains. The Ig domains are classical folds of two antiparallel β sheets, linked by one or two disulphide bonds.

The extracellular part is heavily glycosylated with eight potential N-linked glycosylation sites. The N-glycosylation at asparagine-54 in the first Ig domain of the protein was shown to be essential for the dendrititic membrane-specific distribution of ICAM-5. The mutated ICAM-5 with an unglycosylatable amino acid at position 54 was functionally impaired (Ohgomori et al. 2012).

Another specific feature of ICAM-5 is the distribution of charge in the extracellular part. The crystal structure of the four first Ig domains revealed that the two first domains contain patches of positive charges, while the third to the fifth Ig domains are negatively charged. The extracellular domain has a bent conformation with two sharp angles on either side on Ig domain-3 (Recacha et al. 2014). Interestingly, the intracellular tail has a segment highly enriched in the amino acids alanine and glycine. Their function, if any, remains to be determined.

Function and Binding Partners

As a molecule exclusively expressed in the central nervous system, ICAM-5 is involved in the development of neurons and synaptic maturation. Among the ICAMs, ICAM-5 is exclusive in its ability of homophilic binding. This interaction has been suggested to play an important role especially during early development, where it could promote the outgrowth of neurites (Tian et al. 2000). Later in neuronal development, ICAM-5 acts as a negative regulator of spine maturation by slowing down the transition from filopodia to mushroom spines (Matsuno et al. 2006). The domains -1 and -2 in contact with domains -4 and -5 on another ICAM-5 have been implicated in providing adhesion in the homophilic interactions, as is illustrated in Fig. 2a (Recacha et al. 2014; Tian et al. 2000).
Intercellular Adhesion Molecule-5, Fig. 2

In (A), the homophilic binding of ICAM-5 is shown. (B) shows the structures of Ig domains 1–4 (Modified from Recacha et al. 2014)

All ICAMs bind to the lymphocyte function-associated antigen 1, LFA-1 (CD11a/CD18, αL/β2). LFA-1 is a leukocyte-specific integrin. The integrins are heterodimeric adhesion proteins with a wide expression profile. They consist of one α subunit and one β subunit. There are 18 different α subunits and 8 β subunits. The integrins can promote signaling both inside-out and outside-in. In the brain, ICAM-5 could potentially interact with resident microglia and infiltrating lymphocytes, expressing LFA-1.

The first two Ig domains of ICAM-5 have been crystallized in complex with the I-domain of the α chain of LFA-1, and the glutamic acid-37 was found to be essential for this ligand-receptor interaction (Zhang et al. 2008).

Activation of N-methyl-d-aspartic acid, NMDA, receptors induces shedding of the extracellular portion of ICAM-5. This is mediated by matrix metalloproteases, mainly MMP-2 and -9 (Tian et al. 2007). MMPs are zinc-dependent proteases released in a pro-form. Once activated in the extracellular space, they can target several substrates. ICAM-5 is cut at two sites, generating two major fragments of approximately 85 kDa and 110 kDa. ICAM-5 dissociation from the actin cytoskeleton promotes the cleavage (Tian et al. 2008). The shedding also occurs during early long-term potentiation, LTP (Conant et al. 2010). The soluble ICAM-5 could promote spine and synaptic maturation by (1) binding to β1 integrins leading to subsequent phosphorylation of cofilin (Conant et al. 2011); (2) increasing GluA1 phosphorylation and trafficking to the plasma membrane, increasing the frequency of mini excitatory postsynaptic currents, mEPSC; and (3) inducing elongation of filopodia. Interestingly, ablation of ICAM-5 also increases the mEPSC frequency (Ning et al. 2013).

The psychostimulant methamphetamine can also induce MMP-mediated shedding of ICAM-5. Methamphetamine treatment caused an elevated level of MMP-9 in the hippocampus and striatum in vivo. In this case, the sICAM-5 was suggested to induce integrin β1-mediated phosphorylation of cofilin and subsequent spine maturation (Conant et al. 2011).

ICAM-5 causes a morphological change in microglia and T-cells and it may be important in their binding to telencephalic dendrites and somas. The immunological function of ICAM-5 is, however, different as compared to that of its sibling, ICAM-1. While the soluble form of ICAM-1 is proinflammatory, ICAM-5 was shown to be immunosuppressive. Soluble ICAM-5 downregulates the T-cell receptor-mediated signaling pathway and decreases the secretion of cytokines. Also, the activation markers CD25, CD40, and CD69 are downregulated (Tian et al. 2008).

In the initial contact between two synaptic elements, ICAM-5 on the dendritic terminal may bind the integrin very late antigen-5, VLA-5 (CD49e/CD29, α5/β1) on the axonal terminal. Here also the binding is mediated through the two first Ig domains of ICAM-5. This interaction reduces the cleavage of ICAM-5 and suggests a juvenilizing effect on the new synapse (Ning et al. 2013).

The intracellular part of ICAM-5 interacts with the actin binding/modifying proteins α-actinin and ezrin and radixin of the ezrin/radixin/moesin, ERM-family. ICAM-5 also binds vitronectin, a component of the extracellular matrix, through the second Ig domain. Sequential to this interaction, ERM proteins get phosphorylated and are recruited to filopodia. This induces morphological changes and the formation of a phagocytic cup structure. The interaction between ICAM-5 and ERM has been implicated in filopodia formation and retardation of spine maturation (Furutani et al. 2012). On the other hand, ICAM-5 was colocalized with α-actinin mainly along dendritic shafts. This interaction has a function in neurite outgrowth and glutamate receptor trafficking. ERM protein and α-actinin binding sites partly overlap in the membrane proximal region of ICAM-5: α-actinin binding at amino acids 866–870 and ERM-proteins binding to 869–882. α-Actinin also binds the GluN1 subunit of the NMDA receptor and there is a partial competition between GluN1 and ICAM-5 binding to α-actinin (Fig. 3) (Ning et al. 2015).
Intercellular Adhesion Molecule-5, Fig. 3

ICAM-5 connects the neuron with the extracellular environment. In the cytoplasm, ICAM-5 interacts with actin binding and modifying proteins. α-Actinin is an antiparallel dimer that links several membrane receptors to the cytoskeleton. ERM-family proteins also bind ICAM-5 when they are activated by phosphorylation. The four most distal Ig domains interacts with the extracellular matrix and other receptor molecules, such as integrins. One special feature of ICAM-5 is the homophilic binding, which plays a role in neurite outgrowth. Within the plasma membrane, ICAM-5 interacts with presenilin 1, which is a part of the gamma secretase complex

Role in Disease

Soluble ICAM-5 can be found in the cerebrospinal fluid and plasma of patients with various diseases. Hypoxic ischemia, acute encephalitis, and temporal-lobe epilepsy have been shown to induce the cleavage of ICAM-5. In epilepsy, studies show reduced amounts of sICAM-5 in patient sera. To date, the only known mechanism causing the cleavage of extracellular ICAM-5 is MMP-mediated proteolysis. Soluble ICAM-5 has been shown to modulate cytokine production. This was shown with T-cells in vitro, and a change in cytokine profile was also observed in Herpes simplex virus infection. The viral gene product UOL was found to bind ICAM-5 and the infection caused a decrease in ICAM-5 expression. A mutated virus lacking the UOL gene showed decreased neurovirulence and a lower level of cytokine production (Tse et al. 2009).

Presenilin-1 and -2 which are part of the gamma-secretase complex can associate with the transmembrane region of ICAM-5. This binding promoted an ARF6-mediated removal of ICAM-5 through an autophagic pathway (Raemaekers et al. 2012). Presenilin-1 is an important player in Alzheimer’s disease since the gamma secretase complex generates the cytotoxic form of the amyloid precursor protein, APP, β-amyloid. In the familial form of Alzheimer’s disease, the APP contains mutated amino acids at the site that binds presenilins. Interestingly, ICAM-5 interacts with the same region of presenilins (Annaert et al. 2001). Around the β-amyloid plaques, the expression of ICAM-5 is decreased. Further research in this field demonstrated a protective role for ICAM-5, dampening β-amyloid-induced apoptosis by activating the ERM-family/phosphatidylinositol-3-kinase/protein kinase B pathway (Yang et al. 2012).

Summary

Cell adhesion is critical in all stages of development and normal physiology. ICAM-5 is a complex and versatile adhesion molecule involved in signaling, regulating maturation of neuronal elements, and serving many other functions beyond adhesion. The expression of ICAM-5 is developmentally regulated and confined to the somatodendritic compartment of mammalian telencephalic neurons.

ICAM-5 can bind ligands on neurons and immune cells. Its cytoplasmic tail binds several actin cytoskeleton modifying proteins which can regulate synaptic maturation processes. Mice devoid of ICAM-5 have neurons with increased amounts of mature synapses and the mice perform slightly better in hippocampal mediated memory tasks, compared to the wild-type mice. However, the phenotype of ICAM-5 knockout mice is mild, and the mice live and reproduce normally.

Taken together, the studies done on ICAM-5 have potentially given interesting insights into higher brain functions mediated by the evolutionally youngest part of the mammalian brain. It seems to play a role in brain development, synaptic maturation, and immunological events. The gene is well conserved between species and still the knockout mice can hardly be told apart from wild-type. For future work it would be important to investigate the signaling capacity of ICAM-5, both intracellularly and extracellularly. These events could further elucidate how the molecule can contribute to synaptic plasticity.

See Also

References

  1. Annaert WG, Esselens C, Baert V, Boeve C, Snellings G, Cupers P, et al. Interaction with telencephalin and the amyloid precursor protein predicts a ring structure for presenilins. Neuron. 2001;32(4):579–89.PubMedCrossRefGoogle Scholar
  2. Conant K, Lonskaya I, Szklarczyk A, Krall C, Steiner J, Maguire-Zeiss K, et al. Methamphetamine-associated cleavage of the synaptic adhesion molecule intercellular adhesion molecule-5. J Neurochem. 2011;118(4):521–32.PubMedCrossRefGoogle Scholar
  3. Conant K, Wang Y, Szklarczyk A, Dudak A, Mattson MP, Lim ST. Matrix metalloproteinase-dependent shedding of intercellular adhesion molecule-5 occurs with long-term potentiation. Neuroscience. 2010;166(2):508–21.PubMedCrossRefPubMedCentralGoogle Scholar
  4. Furutani Y, Kawasaki M, Matsuno H, Mitsui S, Mori K, Yoshihara Y. Vitronectin induces phosphorylation of ezrin/radixin/moesin actin-binding proteins through binding to its novel neuronal receptor telencephalin. J Biol Chem. 2012;287(46):39041–9.PubMedCrossRefPubMedCentralGoogle Scholar
  5. Gahmberg CG. Leukocyte adhesion: CD11/CD18 integrins and intercellular adhesion molecules. Curr Opin Cell Biol. 1997;9(5):643–50.PubMedCrossRefGoogle Scholar
  6. Matsuno H, Okabe S, Mishina M, Yanagida T, Mori K, Yoshihara Y. Telencephalin slows spine maturation. J Neurosci. 2006;26(6):1776–86.PubMedCrossRefGoogle Scholar
  7. Mitsui S, Saito M, Hayashi K, Mori K, Yoshihara Y. A novel phenylalanine-based targeting signal directs telencephalin to neuronal dendrites. J Neurosci. 2005;25(5):1122–31.PubMedCrossRefGoogle Scholar
  8. Mori K, Fujita SC, Watanabe Y, Obata K, Hayaishi O. Telencephalon-specific antigen identified by monoclonal antibody. Proc Natl Acad Sci U S A. 1987;84(11):3921–5.PubMedCrossRefPubMedCentralGoogle Scholar
  9. Ning L, Paetau S, Nyman-Huttunen H, Tian L, Gahmberg CG. ICAM-5 affects spine maturation by regulation of NMDA receptor binding to α-actinin. Biol Open. 2015;4(2):125–36.PubMedCrossRefPubMedCentralGoogle Scholar
  10. Ning L, Tian L, Smirnov S. Interactions between intercellular adhesion molecule-5 (ICAM-5) and b1 integrins regulate neuronal synapse formation. J Cell Sci. 2013;126(1):77–89.PubMedCrossRefPubMedCentralGoogle Scholar
  11. Ohgomori T, Nanao T, Morita A, Ikekita M. Asn54-linked glycan is critical for functional folding of intercellular adhesion molecule-5. Glycoconj J. 2012;29(1):47–55.PubMedCrossRefGoogle Scholar
  12. Raemaekers T, Peric A, Baatsen P, Sannerud R, Declerck I, Baert V, et al. ARF6-mediated endosomal transport of Telencephalin affects dendritic filopodia-to-spine maturation. EMBO J. 2012;31(15):3252–69.PubMedCrossRefPubMedCentralGoogle Scholar
  13. Recacha R, Jiménez D, Tian L, Barredo R, Gahmberg CG, Casasnovas JM. Crystal structures of an ICAM-5 ectodomain fragment show electrostatic-based homophilic adhesions. Acta Crystallogr D Biol Crystallogr. 2014;70(Pt 7):1934–43.PubMedCrossRefPubMedCentralGoogle Scholar
  14. Tian L, Lappalainen J, Autero M, Hanninen S, Rauvala H, Gahmberg CG. Shedded neuronal ICAM-5 suppresses T-cell activation. Blood. 2008;111(7):3615–25.PubMedCrossRefGoogle Scholar
  15. Tian L, Nyman H, Kilgannon P, Yoshihara Y, Mori K, Andersson LC, et al. Intercellular adhesion molecule-5 induces dendritic outgrowth by homophilic adhesion. J Cell Biol. 2000;150(1):243–52.PubMedCrossRefPubMedCentralGoogle Scholar
  16. Tian L, Stefanidakis M, Ning L, Van Lint P, Nyman-Huttunen H, Libert C, et al. Activation of NMDA receptors promotes dendritic spine development through MMP-mediated ICAM-5 cleavage. J Cell Biol. 2007;178(4):687–700.PubMedCrossRefPubMedCentralGoogle Scholar
  17. Tse MCL, Lane C, Mott K, Onlamoon N, Hsiao HM, Perng GC. ICAM-5 modulates cytokine/chemokine production in the CNS during the course of herpes simplex virus type 1 infection. J Neuroimmunol. 2009;213(1–2):12–9.PubMedCrossRefPubMedCentralGoogle Scholar
  18. Yang H, Wu D, Zhang X, Wang X, Peng Y, Hu Z. Telencephalin protects PAJU cells from amyloid beta protein-induced apoptosis by activating the ezrin/radixin/moesin protein family/phosphatidylinositol-3-kinase/protein kinase B pathway. Neural Regen Res. 2012;7(28):2189–98.PubMedPubMedCentralGoogle Scholar
  19. Yoshihara Y, Oka S, Nemoto Y, Watanabe Y, Nagata S, Kagamiyama H, et al. An ICAM-related neuronal glycoprotein, telencephalin, with brain segment-specific expression. Neuron. 1994;12(3):541–53.PubMedCrossRefGoogle Scholar
  20. Zhang H, Casasnovas JM, Jin M, Liu JH, Gahmberg CG, Springer TA, et al. An unusual allosteric mobility of the C-terminal helix of a high-affinity alphaL integrin I domain variant bound to ICAM-5. Mol Cell. 2008;31(3):432–7.PubMedCrossRefPubMedCentralGoogle Scholar

Copyright information

© Springer International Publishing AG 2018

Authors and Affiliations

  1. 1.Department of Biosciences, Division of Biochemistry and Biotechnology, Faculty of Biological and Environmental SciencesUniversity of HelsinkiHelsinkiFinland