Zusammenfassung
Angeborene Anomalien der Koronargefäße finden sich in 0,2–1,2% der Bevölkerung und können mit erheblicher Morbidität und Mortalität assoziiert sein. Diese Arbeit liefert eine Übersicht zum aktuellen Stand aus Sicht der Embryologie (Teil I) und zur klinischen Diagnostik und Therapie (Teil II).
Im vorliegenden ersten Teil der Arbeit bieten wir eine Übersicht zur koronaren Vaskulogenese, Angiogenese und embryonalen Arteriogenese. Hierbei beleuchten wir besonders die Rolle von Vorläuferzellen wie beispielsweise der epikardialen Vorläuferzellen, der kardialen Neuralleistenzellen und Vorläuferzellen des peripheren Reizleitungssystems. Darüber hinaus stellen wir die Rolle verschiedener Wachstumsfaktoren (beispielsweise FGV, HIF 1, PDGF B, TGFβ1, VEGF und VEGFR-2) und Gene (beispielsweise FOG-2, VCAM-1, Bves und RALDH2) bei der Regulation einzelner Schritte der koronaren Gefäßbildung dar.
Dieser Teil der Übersicht möchte die Vielzahl von Möglichkeiten und Mechanismen zur Entstehung koronarer Anomalitäten verdeutlichen. Deshalb verweisen wir besonders auf Ergebnisse aus Experimenten, die eine systematische Beziehung definierter Störungen auf molekularer Ebene mit koronarer Anomalie erkennen lassen. Besonders gehen wir hierbei auf die Rolle der Neuralleiste bei der Entwicklung von Koronaranomalien und deren Assoziation mit Anomalien der Aortenwurzel und Aortenklappe ein.
Summary
Congenital anomalies of the coronary arteries occur in 0.2–1.2% of the general population and may cause substantial cardiovascular morbidity and mortality. We review some of the advances that have been made both, in the understanding of the embryonic development of the coronary arteries (part I) and in the clinical diagnosis and management of their anomalies (part II).
In this first part of our review we elucidate basic mechanisms of coronary vasculogenesis, angiogenesis and embryonic arteriogenesis. Moreover, we review the role of cellular progenitors such as epicardium-derived cells, cardiac neural crest cells and cells of the peripheral conduction system. Then we discuss the role of growths factors (such as FGV, HIF 1, PDGF B, TGFβ1, VEGF, and VEGFR-2) and genes (such as FOG-2, VCAM-1, Bves, and RALDH2) at different states of coronary development. and we discuss the role of the cardiac neural crest in the concurrence of coronary anomalies with aortic root malformations.
This part of the article is designed to review major determinants of coronary vascular development to provide a better understanding of the multiplicity of options and mechanisms that may give rise to coronary anomaly. To this end, we highlight results from experiments that provide insight in mechanisms of coronary malformation
References
Angelini P, Villason S, Chan AVJ, Diez JG (1999) Normal and anomalous coronary arteries in humans. In: Angelini P (ed) Coronary artery anomalies: a comprehensive approach. Williams & Wilkins, Lippincott, Philadelphia, pp 27–150
Bernanke DH, Valkey JM (2002) Development of the coronary blood supply: changing concepts and current ideas. Anat Rec (New Anat) 269:198–208
Bockmann DE, Redmond ME, Kirby ML (1989) Alteration of early vascular development after ablation of cranial neural crest. Anat Rec 225:209–217
Bogers AJ, Gittenberger-de Groot AC, Poelmann RE, Peault BM, Huysmans HA (1989) Development of the origin of the coronary arteries, a matter of ingrowth or outgrowth? Anat Embryol (Berl) 180:437–441
Cardo M, Fernandez B, Duran AC, Fernandez MC, Arque JM, Sans-Coma V (1995) Anomalous origin of the left coronary artery from the dorsal aortic sinus and its relationship with aortic valve morphology in Syrian hamsters. J Comp Pathol 112:373–380
Carmeliet P (2003) Angiogenesis in health and disease. Nature Medicine 9:653–660
Cheng G, Litchenberg WH, Cole GJ, Mikawa T, Thompson RP, Gourdie RG (1999) Development of the cardiac conduction system involves recruitment within a multipotent cardiomyogenic lineage. Development 126:5041–5049
Crispino JD, Lodish MB, Thurberg BL, Litovsky SH, Collins T, Molkentin JD, Orkin SH (2001) Proper coronary vascular development and heart morphogenesis depend on interaction of GATA-4 with FOG cofactors. Genes Dev 15:839–844
DeRuiter MC, Poelmann RE, Vander-Plas-de Vries I, Mentink MM, Gittenberger-de Groot AC (1992) The development of the myocardium and endocardium in mouse embryos. Fusion of two heart tubes? Anat Embryol (Berl) 185:461–473
Doty DB (2001) Anomalous origin of the left circumflex coronary artery associated with a bicuspid aortic valve. J Thorac Cardiovasc Surg 122:842–843
Fedak PWM, Verma S, David TE, Leask RL, Weisel RD, Butany J (2002) Clinical and pathophysiological implications of a bicuspid aortic valve. Circulation 106:900–904
Ferrara N, Gerber HP, LeCouter J (2003) The biology of VEGF and its receptors. Nature Medicine 9:669–676
Fukiishi Y, Morris-Kay GM (1992) Migration of cranial neural crest cells to the pharyngeal arches and heart in rat embryos. Cell Tissue Res 268:1–8
Gittenberger-de Groot AC, Vrancken Peeters MP, Mentink MM, Gourdie RG, Poelmann RE (1998) Epicardium-derived cells contribute a novel population to the myocardial wall and the atrioventricular cushions. Circ Res 82:1043–1052
Harris BS, O’Brien TX, Gourdie RG (2002) Coronary arteriogenesis and differentiation of periarterial Purkinje fibers in the chick heart: is there a link? Tex Heart Inst J 29:262–270
Helisch A, Schaper W (2000) Angiogenesis and arteriogenesis—not yet for prescription. Z Kardiol 89:239–244
Hidai H, Bardales R, Goodwin R, Quertermous T, Quertermous EE (1998) Cloning of capsulin, a basic helix-loop-helix factor expressed in progenitor cells of the pericardium and the coronary arteries. Mech Dev 73:33–43
Higgins CB, Wexler L (1975) Reversal of dominance of the coronary arterial system in isolated aortic stenosis. Circulation 52:292–296
Hutchins GM, Nazarian IH, Bulkley BH (1978) Association of left dominant coronary arterial system with congenital bicuspid aortic valve. Am J Cardiol 42:57–59
Jain RK (2003) Molecular regulation of vessel maturation. Nature Medicine 9:685–693
Kappetein AP, Gittenberger de Groot AC, Zwinderman AH, Rohmer J, Poelmann RE, Huysmans HA (1991) The neural crest as a possible pathogenetic factor in coarctation of the aorta and bicuspid aortic valve. J Thorac Cardiovasc Surg 102:830–836
Kirby ML, Gale TF, Steward DE (1983) Neural crest cells contribute to normal aorticopulmonary septation. Science 220:1059–1061
Kirby ML (1989) Plasticity and predetermination of the mesencephalic and trunk neural crest transplanted into the region of cardiac neural crest. Dev Biol 134:402–412
Kirby ML, Waldo KL (1990) Role of neural crest in congenital heart disease. Circulation 82:332–340
Kirby ML, Hunt P, Wallis K, Thorogood P (1997) Abnormal patterning of the aortic arch arteries does not evoke cardiac malformations. Dev Dyn 208:34–47
Kroll J, Waltenberger J (2000) Regulation of the endothelial function and angiogenesis by vascular endothelial growth factor-A (VEGF-A). Z Kardiol 89:206–218
Kubalak SW, Sucov HM (1999) Retinoids in heart development. In: Harvey RP, Rosenthal N (eds) Heart development. Academic Press, San Diego, pp 209–219
Lu J, Landerholm TE, Wei JS, Dong XR, Wu SP, Liu X, Nagata K, Inagaki M, Majesky MW (2001) Coronary smooth muscle differentiation from proepicardial cells requires rhoA-mediated actin reorganization and p160 rho-kinase activity. Dev Biol 240:404–418
Manner J (1993) Experimental study on the formation of the epicardium in chick embryos. Anat Embryol (Berl) 187:281–289
Manner J (1999) Does the subepicardial mesenchyme contribute myocardioblasts to the myocardium of the chick embryo heart? A quail-chick chimera study tracing the fate of the epicardial primordium. Anat Rec 255:212–226
Morabito CJ, Dettman RW, Kattan J, Collier JM, Bristow J (2001) Positive and negative regulation of epicardial-mesenchymal transformation during avian heart development. Dev Biol 234:204–215
Moss JB, Xavier-Neto J, Shapiro MD, Nayeem SM, McCaffery P, Drager UC, Rosenthal N (1998) Dynamic patterns of retinoic acid synthesis and response in the developing mammalian heart. Dev Biol 199:55–71
Munoz-Chapuli R, Gonzalez-Iriarte M, Carmona R, Atencia R, Macias D, Perez-Pomares JM (2002) Cellular precursors of the coronary arteries. Tex Heart Inst J 29:243–249
Murphy ES, Rosch J, Rahimtoola S (1977) The frequency and significance of coronary arterial dominance in isolated aortic stenosis. Am J Cardiol 39:505–509
Nishibatake M, Kirby ML, van Mierop LH (1987) Pathogenesis of persistent truncus arteriosus and dextroposed aorta in the chick embryo after neural crest ablation. Circulation 75:255–264
Noden DM (1983) The role of the neural crest in patterning of avian cranial skeletal connective, and muscle tissue. Dev Biol 96:144–165
Palamo AR, Schrager BR, Chahine RA (1995) Anomalous origin of the right coronary artery from the ascending aorta high above the left posterior sinus of Valsalva of a bicuspid aortic valve. Am Heart J 109:902–904
Poelmann RE, Lie-Venema H, Gittenberger-de Groot AC (2002) The role of the epicardium and neural crest as extracardiac contributors to coronary vascular development. Tex Heart Inst J 29:255–261
Poole TJ, Coffin JD (1989) Vasculogenesis and angiogenesis: two distinct morphogenetic mechanisms establish embryonic vascular pattern. J Exp Zool 251:224–231
Potts JD, Dagle JM, Walder JA, Weeks DL, Runyan RB (1991) Epithelial-mesenchymal transformation of embryonic cardiac endothelial cells is inhibited by a modified antisense oligodeoxynucleotide to transforming growth factor beta 3. Proc Natl Acad Sci USA 88:1516–1520
Pugh CW, Ratcliffe PJ (2003) Regulation of angiogenesis by hypoxia: role of the HIF system. Nature Medicine 9:677–684
Reese DE, Mikawa T, Bader DM (2002) Development of the coronary vessel system. Circ Res 91:761–768
Resnick N, Gimbrone MAJ (1995) Hemodynamic forces are complex regulators of endothelial gene expression. FASEB J 9:874–882
Risau W, Flamme I (1995) Vasculogenesis. Annu Rev Cell dev Biol 11:73–91
Risau W (1997) Mechanisms of angiogenesis. Nature 386:671–674
Sans-Coma V, Arque JM, Duran AC, Cardo M, Fernandez B (1991) Coronary artery anomalies and bicuspid aortic valves in the Syrian hamster. Basic Res Cardiol 86:148–153
Schaper W, Piek JJ, Munoz-Chapuli R, Wolf C, Ito W (1999) Collateral circulation of the heart. In: Ware JA, Simons M (eds) Angiogenesis and cardiovascular disease. University Press, New York Oxford, pp 159–198
Sumida H, Akimoto N, Nakamura H (1989) Distribution of the neural crest cells in the heart of birds: a three dimensional analysis. Anat Embryol 180:29–35
Takamura K, Okishima T, Ohdo S, Hayakawa K (1990) Association of cephalic neural crest cells with cardiovascular development, particularly that of the semilunar valves. Anat Embryol 182:263–272
Tevosian SG, Deconinck AE, Tanaka M, Schinke M, Litovsky SH, Izumo S, Fujiwara Y, Orkin SH (2000) FOG-2, a cofactor for GATA transcription factors, is essential for heart morphogenesis and development of the coronary vessels from epicardium. Cell 101:729–739
Tomanek RJ, Lotun K, Clark EB, Suvarna PR, Hu N (1998) VEGF and bFGF stimulate myocardial vascularization in embryonic chick. Am J Physiol 274(5 Pt 2):H1620–1626
Tomanek RJ, Zheng W, Peters KG, Lin P, Holifield JS, Suvarna PR (2001) Multiple growth factors regulate coronary embryonic vasculogenesis. Dev Dyn 221:265–673
Tomanek RJ, Zheng W (2002) Role of growth factors in coronary morphogenesis. Tex Heart Inst J 29:250–254
Van Mierop LHS, Kutsche LM (1986) Cardiovascular anomalies in Di-George syndrome and importance of neural crest as possible pathogenetic factor. Am J Cardiol 58:133–137
von Kodolitsch Y, Aydin AM, Koschyk DH, Loose R, Schalwat I, Karck M, Cremer J, Haverich A, Berger J, Meinertz T, Nienaber A (2002) Predictors of aneurysm formation after surgical correction of aortic coarctation. J Am Coll Cardiol 39:617–624
Vrancken Peeters MP, Gittenberger-de Groot AC, Mentink MM, Poelmann RE (1999) Smooth muscle cells and fibroblasts of the coronary arteries derive from epithelial-mesenchymal transformation of the epicardium. Anat Embryol (Berl) 199:367–378
Wada AM, Reese DE, Bader DM (2001) Bves: prototype of a new class of cell adhesion molecules expressed during coronary artery development. Development 128:2085–2093
Xavier-Neto J, Shapiro MD, Houghton L, Rosenthal N (2000) Sequential programs of retinoic acid synthesis in the myocardial and epicardial layers of the developing avian heart. Dev Biol 219:129–141
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von Kodolitsch, Y., Ito, W.D., Franzen, O. et al. Coronary artery anomalies. Z Kardiol 93, 929–937 (2004). https://doi.org/10.1007/s00392-004-0152-7
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DOI: https://doi.org/10.1007/s00392-004-0152-7
Schlüsselwörter
- Angiogenese
- Gefäße
- Embryologie
- Reizleitung
- Endotheliale Wachstumsfaktoren
- Endothel
- Neuralleiste
- Stammzellen
- Koronararterien