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Current cell biology textbooks mention only two kinds of cell-to-cell adhering junctions coated with the cytoplasmic plaques: the desmosomes (maculae adhaerentes), anchoring intermediate-sized filaments (IFs), and the actin microfilament-anchoring adherens junctions (AJs), including both punctate (puncta adhaerentia) and elongate (fasciae adhaerentes) structures. In addition, however, a series of other junction types has been identified and characterized which contain desmosomal molecules but do not fit the definition of desmosomes. Of these special cell-cell junctions containing desmosomal glycoproteins or proteins we review the composite junctions (areae compositae) connecting the cardiomyocytes of mature mammalian hearts and their importance in relation to human arrhythmogenic cardiomyopathies. We also emphasize the various plakophilin-2-positive plaques in AJs (coniunctiones adhaerentes) connecting proliferatively active mesenchymally-derived cells, including interstitial cells of the heart and several soft tissue tumor cell types. Moreover, desmoplakin has also been recognized as a constituent of the plaques of the complexus adhaerentes connecting certain lymphatic endothelial cells. Finally, we emphasize the occurrence of the desmosomal transmembrane glycoprotein, desmoglein Dsg2, out of the context of any junction as dispersed cell surface molecules in certain types of melanoma cells and melanocytes. This broadening of our knowledge on the diversity of AJ structures indicates that it may still be too premature to close the textbook chapters on cell-cell junctions.
Typicaldesmosomes (maculae adhaerentes) are cell-cell junctions connecting cells of epithelial, meningothelial,and myocardial nature or malignantly transformed cells derived therefrom. Over the past two decades the molecular and ultrastructuralorganization of diverse cell-cell-connecting plasma membrane structures has been elucidated and two novel categories and architectonic principles have been recognized: desmosomal molecules as functionally important components of special non-desmosomal junctions and the existence of certain desmosomal molecules in a non-junction-bound form.
The ultrastructural organization and the high lateral packing density of desmosomes in the epidermis or other multistratified vertebrate epithelia is best seen in the electron microscope (e.g., Figure 1), and the corresponding protein compositions of the various desmosomal subtypes in the specific strata have been determined by biochemical analyses and immunolocalization techniques [1–7].
In most stratified epithelia, epidermis included, the desmosome packing density is so high that more than half of the entire cell-cell membrane contact area is represented by desmosomal structures. Using immunohistochemical techniques with desmosomal markers this high packing density is directly demonstrable not only for all layers of the highly cornified mammalian epidermis but also in the skin of lower vertebrates such as fishes and amphibia (Figure 2(a) shows the immunolocalization of plakoglobin on a section of fixed, paraffin-embedded skin of the eel, Anguilla anguilla; Figure 2(b) shows desmoplakin immunostaining on the skin of the frog, Rana pipiens; for details see ). Clearly, in stratified epithelia the desmosomal constituents are, together with the keratin filaments, among the most frequent proteins. Moreover, the molecular composition of the epidermal desmosomes—and those of similar multistratified epithelia—has been found to show fundamental strata- specific differences, notably with respect to the desmogleins, Dsg1-4, the desmocollins, Dsc1-3, and the plaque proteins plakophilins, Pkp1-3 (Table 1 and [4–6, 9]).
The stratum-specific molecular ensembles, specifically the Dsg and Dsc glycoproteins, are also of marked importance with respect to the pathogenesis of autoimmune skin diseases of the pemphigus type which show a more or less direct correlation with the specific desmosomal glycoprotein complement of the affected layer (see, e.g., [4, 6, 9, 24–28]). These autoimmune diseases are specifically dealt within other articles of this issue. Another aspect of the desmosomal arrays in the epidermis and other stratified epithelia is their frequent—in some areas almost regular—punctuation by very small “sandwich junctions” (iuncturae structae) containing the four times-membrane-spanning tight junction hallmark protein, occludin [29, 30].
In mammals the development of the ID junctional system connecting cardiomyocytes does not stop at birth but continues postnatally [15, 31, 32]. In particular the two types of adhering junctions originally distinguishable show further polar translocation, accumulation in the ID region and fusions of the desmosomal and the fascia adhaerens components, accompanied by an increasing amalgamation of the two kinds of molecular ensembles into the new mixed category of area composita (AC) structures (Figures 3(a)–3(c), 4(b), and 5(a); for details of molecular localizations and biochemical analyses see [14, 15, 33]; for non-mammalian species see however [8, 34]). As a typical result rather extended AC structures are seen which combine compositional and ultrastructural properties of desmosomes with those of AJs (Figures (Figures3 and3 and 4(b)). In addition, the “mixed AC ensembles” of the ID (Table 1; Figure 4(b)) include a series of additional proteins such as α-T-catenin  and the recently identified plaque protein called “myozap” . The special organizational importance of certain armadillo-type proteins, in particular plakoglobin and plakophilin-2, for the entire ID contact of cardiomyocytes has also been demonstrated for early stages of murine heart formation in the absence of the genes encoding these proteins [35, 36] and in siRNA-downregulation experiments ([37–39], for related experiments see also [40, 41]).
The physiological and medical importance of desmosomal molecules in the composite junctions of the myocardiac IDs is most impressively demonstrated by the recent avalanche of publications that specific mutations in genes encoding desmosomal proteins can result in arrhythmogenic cardiomyopathies (ARVC/D), mostly in the right ventricle but left ventricle damages have also been reported (Table 2). Here the gene encoding plakophilin-2 appears to be especially vulnerable as defects in this gene alone seem to account for about two thirds of the cases. This category of ARVC/D-based diseases and “sudden death” events resulting from altered desmosomal proteins also includes complex hereditary syndromes such as combinations of dermatological disorders (“woolly hair”, diverse patterns of striate and diffuse keratoderma changes, particularly in palmoplantar skin) and cardiac disease features such as in the classic “Naxos disease” type or the “Carvajal syndrome” subtype, first identified in the year 2000 in three Ecuadorian families, which may also include damages inboth ventricles (for an anthology see ). The specific dominant and recessive forms of the human diseases ascribed to mutations of genes encoding desmosomal proteins have been dealt with in several specific recent review articles [42, 97–102].
The specialized cells of the mammalian cardiac conduction system are connected by three different types of AJs : desmosomes, which in certain cell regions occur in impressively high packing density, as well as AJs and CJs (Figures 5(b)–5(d)). The conductive cells of the ovine and bovine Purkinje fiber systems have been studied in special detail with respect to their nature as modified cardiomyocytes and to the various forms of junctions of which a major proportion is located at lateral cell-cell contact sites [103–105]. These findings have led to the hypothesis that the abundance of apparently “normal-looking” desmosomes in the conductive tissue might also—and perhaps primarily—be affected by the desmosomal protein mutations in cases of human ARVC/D (Table 2), as also suggested from the much higher conduction speed of these “cell fibers” (see, e.g., [103, 106, 107]).
The various size classes of the desmosomal protein-rich junctions connecting conduction cells are presented by desmoplakin immunoelectron microscopy in Figures 5(b)–5(d), including some very small junctions(arrowheads in Figure 5(b)). Frequently, a number of individual desmin-containing intermediate filaments can be resolved at such junctions (e.g., Figure 5(c)), often revealing closely-parallel plaque associations (e.g., arrows in Figure 5(d)).
Proteins of the plakophilin-subfamily of armadillo proteins are constitutive, apparently necessary components of desmosomal plaques [13, 108–113]. Their special organizational role and architectonic importance has been demonstrated perhaps most convincingly in the case of plakophilin-2 by gene abrogation as well as siRNA-mediated mRNA reduction experiments [36, 37, 39–41]. Moreover, the functional importance of some plakophilins, in particular plakophilin-2, may extend beyond desmosomal plaques to gap junctions [37, 38] and into the interior of the cell, including certain cytoplasmic as well as nuclear complexes [114–116].
Recently, however, we have discovered that the occurrence of both plakophilin-2 and plakophilin-3 is not necessarily restricted to the plaques of desmosomes but that these proteins can also occur as constitutive molecules in plaques of some non-desmosomal junctions such as the puncta adhaerentia-like AJs of certain cell cultures [22, 23, 117] or in proliferatively active cells of certain tumors, for example in cardiac myxomata . Here the rapid acquisition of plakophilin-2 to the non-desmosomal plaques of these tumor cell AJs, in particular the fact that it appears in the earliest in vitro culture passages of cardiac valvular interstitial cells from various mammalian species , suggests that the addition of plakophilin-2 alone—or together with plakophilin-3—to these junctions is somehow related to the induction of proliferation and cell cycle growth. It is therefore likely that in the future the systematic examination of the presence of plakophilins in such AJs will give valuable diagnostic informations. Figures 6(a)–6(e) present the early integration of plakophilin-2 into a series of small puncta adhaerentia connecting interstitial cells freshly brought from cardiac valve matrix tissue into cell culture (for details see ).
The junctional system connecting the endothelial cells of blood and lymph vessels is obviously of great biological importance and has been studied extensively (reviews: [119, 120]). There is, however, a special category of variously-sized and -shaped AJs which connect certain types of endothelial cells in some parts of the lymphatic system, including the three-dimensionally branched “virgultar” cells of lymph node sinus as well as specific cutaneous and other peripheral lymph capillaries, which are characterized by AJs containing in addition desmoplakin as a major plaque protein, in most cases probably in combination with plakoglobin [18, 121–123]. The existence of such complexus adhaerentes in special parts of the vascular endothelial system has since been confirmed several times ([124–126], for a recent review see ). The formation of plaque complexes of VE-cadherin with desmoplakin and plakoglobin has also been demonstrated for dermal capillary endothelium in special molecular assembly experiments .
Beyond this role of desmoplakin as a regular constituent of the plaques of such “complex junctions” in certain lymphatic endothelia of the mature body a fundamental and general role of desmoplakin in the formation of the vascular endothelial system is also indicated by the transgene embryogenesis studies of Gallicano et al. [128, 129]. Thus, the complexus adhaerens junctions have to be added to the list of novel kinds of adhering junctions in their own right (see Table 1; for recent reviews see: [19, 130, 131]).
Desmosomal cadherins typically associate with each other and form close-packed cis-clusters in the membranes of cytoplasmic vesicles, then exocytose to form a “half-junction” on the cell surface and under sufficient Ca2+-concentration may further associate head-to-head in transform with another “half-junction”, usually a domain of an adjacent cell, to a symmetrical junction [132–137]. Isolated, that is, non-junction-bound, desmosomal cadherin molecules that have not been included in desmosome structures and consequently may be dispersed over extended parts of the plasma membrane until recently had not been observed in natural cells. Only in certain cell culture lines deficient of most junction components such as the human fibrosarcoma HT-1080 cells states of the isolated desmosomal cadherin, Dsg2, have been described to occur on cell surfaces and could be integrated into junction-like structures only upon introduction of further desmosomal proteins [137, 138].
Thus it was with great surprise when we noted the occurrence of Dsg2 molecules dispersed over large portions of the surface membrane of certain cultures of human melanocytes or neval cells as well as on surfaces of a subtype of melanoma cells in situ and in culture [139, 140]. As far as it could be concluded from the biochemical analyses and immunolocalization experiments so far performed, these Dsg2 glycoprotein molecules were not stably complexed with specific other transmembrane or with any plaque molecules but nevertheless seemed to be somehow involved in close membrane-to-membrane associations. It is obvious that such stages, that is, dispersed, non-junction-bound desmosomal cadherins will have to be studied with special care as they point to the existence of yet unknown, radically different cell-cell adhesion mechanisms involving desmosomal cadherins.
The authors thank Caecilia Kuhn and Christine Grund for their excellent technical assistance, the “Deutsche Krebshilfe” (Grant 10-2049-Fr1 to W. W. Franke), and the German Ministry for Research and Technology (Program Regenerative Medicine, START-MSC, to W. W. Franke) for financial support. Sebastian Pieperhoff thanks in particular the Canadian Government (DFAIT) for funding of a Postodoctoral Research Fellowship (PDRF) during the tenure 03/2008–03/2009 and the German Science Foundation (DFG) for funding of a Postodctoral Research Fellowship during the following tenure.