Kindlin-2 Is an Essential Component of Intercalated Discs and Is Required for Vertebrate Cardiac Structure and Function

Integrins and proteins that associate with integrins are implicated in normal cardiac muscle function and development. Unc-112 is a cytoplasmic adaptor protein required for the proper establishment of integrin junctions in Caenorhabditis elegans muscle. A vertebrate homolog of unc-112, kindlin-2, is an integrin-binding protein that is expressed in cardiac muscle, but its function is unknown. We sought to understand the role of kindlin-2 in the development and function of the mouse and zebrafish heart. In the mouse, we found that kindlin-2 is highly expressed in the heart and is enriched at intercalated discs and costameres. Targeted disruption of the murine kindlin-2 gene resulted in embryonic lethality before cardiogenesis. To better assess the role of kindlin-2 in cardiac muscle development, we used morpholinos to knockdown the kindlin-2 homolog in zebrafish (z-kindlin-2), which resulted in severe abnormalities of heart development. Morphant hearts were hypoplastic and dysmorphic and exhibited significantly reduced ventricular contractility. Ultrastructural analysis of these hearts revealed disrupted intercalated disc formation and a failure in the attachment of myofibrils to membrane complexes. We conclude that kindlin-2 is an essential component of the intercalated disc, is necessary for cytoskeletal organization at sites of membrane attachment, and is required for vertebrate myocardial formation and function. These findings provide the first characterization of the in vivo functions of this novel and critical regulator of cardiogenesis.

[1]  N. Schork,et al.  Laminin-&agr;4 and Integrin-Linked Kinase Mutations Cause Human Cardiomyopathy Via Simultaneous Defects in Cardiomyocytes and Endothelial Cells , 2007 .

[2]  J. Qin,et al.  The MIG-2/Integrin Interaction Strengthens Cell-Matrix Adhesion and Modulates Cell Motility* , 2007, Journal of Biological Chemistry.

[3]  S. Dedhar,et al.  Integrin-Linked Kinase at the Heart of Cardiac Contractility, Repair, and Disease , 2007, Circulation research.

[4]  R. Hauer,et al.  Molecular genetics of arrhythmogenic right ventricular cardiomyopathy: emerging horizon? , 2007, Current opinion in cardiology.

[5]  Xueying Lin,et al.  Depletion of Zebrafish Titin Reduces Cardiac Contractility by Disrupting the Assembly of Z-Discs and A-Bands , 2007, Circulation research.

[6]  N. Schork,et al.  Laminin-alpha4 and integrin-linked kinase mutations cause human cardiomyopathy via simultaneous defects in cardiomyocytes and endothelial cells. , 2007, Circulation.

[7]  Ping Hu,et al.  Integrin Activation in the Heart: A Link Between Electrical and Contractile Dysfunction? , 2006, Circulation research.

[8]  P. Ellinor,et al.  Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy. , 2006, American journal of human genetics.

[9]  U. Schlötzer-Schrehardt,et al.  Kindlin-1 Is a Phosphoprotein Involved in Regulation of Polarity, Proliferation, and Motility of Epidermal Keratinocytes* , 2006, Journal of Biological Chemistry.

[10]  Hao-Ven Wang,et al.  The Kindlins: subcellular localization and expression during murine development. , 2006, Experimental cell research.

[11]  S. Nattel,et al.  Targeted ablation of ILK from the murine heart results in dilated cardiomyopathy and spontaneous heart failure. , 2006, Genes & development.

[12]  W. Rottbauer,et al.  Integrin-linked kinase, a novel component of the cardiac mechanical stretch sensor, controls contractility in the zebrafish heart. , 2006, Genes & development.

[13]  M. Russell,et al.  Obscurin is required for the lateral alignment of striated myofibrils in zebrafish , 2006, Developmental dynamics : an official publication of the American Association of Anatomists.

[14]  Z. Khuchua,et al.  A Zebrafish Model of Human Barth Syndrome Reveals the Essential Role of Tafazzin in Cardiac Development and Function , 2006, Circulation research.

[15]  Emilio Hirsch,et al.  Integrin signalling: the tug-of-war in heart hypertrophy. , 2006, Cardiovascular research.

[16]  Qin Liu,et al.  Cadherin2 (N-cadherin) plays an essential role in zebrafish cardiovascular development , 2006, BMC Developmental Biology.

[17]  Chuanyue Wu Migfilin and its binding partners: from cell biology to human diseases , 2005, Journal of Cell Science.

[18]  Qiang Zhou,et al.  A Cypher/ZASP Mutation Associated with Dilated Cardiomyopathy Alters the Binding Affinity to Protein Kinase C* , 2004, Journal of Biological Chemistry.

[19]  M. Beckerle,et al.  The Kindler Syndrome Protein Is Regulated by Transforming Growth Factor-β and Involved in Integrin-mediated Adhesion* , 2004, Journal of Biological Chemistry.

[20]  S. Kudoh,et al.  A novel LIM protein Cal promotes cardiac differentiation by association with CSX/NKX2-5 , 2004, The Journal of cell biology.

[21]  A. Sonnenberg,et al.  Erratum: Integrins in regulation of tissue development and function. J Pathol; 200: 471–480 , 2003 .

[22]  M. Lohse,et al.  Disruption of cardiac Ena-VASP protein localization in intercalated disks causes dilated cardiomyopathy. , 2003, American journal of physiology. Heart and circulatory physiology.

[23]  H. Feiler,et al.  Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome. , 2003, American journal of human genetics.

[24]  Arnoud Sonnenberg,et al.  Integrins in regulation of tissue development and function , 2003, The Journal of pathology.

[25]  M. Labouesse,et al.  Cell adhesion: parallels between vertebrate and invertebrate focal adhesions , 2003, Current Biology.

[26]  J. Weissenbach,et al.  Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome. , 2003, Human molecular genetics.

[27]  Y. Tu,et al.  Migfilin and Mig-2 Link Focal Adhesions to Filamin and the Actin Cytoskeleton and Function in Cell Shape Modulation , 2003, Cell.

[28]  Takao Sakai,et al.  Integrin-linked kinase (ILK) is required for polarizing the epiblast, cell adhesion, and controlling actin accumulation. , 2003, Genes & development.

[29]  E. Ehler,et al.  Dilated cardiomyopathy: a disease of the intercalated disc? , 2003, Trends in cardiovascular medicine.

[30]  Richard O Hynes,et al.  Integrins Bidirectional, Allosteric Signaling Machines , 2002, Cell.

[31]  D. Moerman,et al.  C. elegans PAT-4/ILK Functions as an Adaptor Protein within Integrin Adhesion Complexes , 2002, Current Biology.

[32]  S. Cherry,et al.  Cardiac Myocyte-Specific Excision of the &bgr;1 Integrin Gene Results in Myocardial Fibrosis and Cardiac Failure , 2002, Circulation research.

[33]  R. Ross,et al.  Integrins and the myocardium. , 2001, Genetic engineering.

[34]  D. Moerman,et al.  The UNC-112 Gene in Caenorhabditis elegansEncodes a Novel Component of Cell–Matrix Adhesion Structures Required for Integrin Localization in the Muscle Cell Membrane , 2000, The Journal of cell biology.

[35]  M. Schaller,et al.  UNC112. A new regulator of cell-extracellular matrix adhesions? , 2000, The Journal of cell biology.

[36]  S. C. Liu,et al.  The FERM domain: A unique module involved in the linkage of cytoplasmic proteins to the membrane , 1998 .

[37]  E. Fuchs,et al.  Beta4 integrin is required for hemidesmosome formation, cell adhesion and cell survival , 1996, The Journal of cell biology.

[38]  R. Pedersen,et al.  Deletion of beta 1 integrins in mice results in inner cell mass failure and peri-implantation lethality. , 1995, Genes & development.