The great vessels are a part of the vascular system that first appears in the mid-third week of development from mesoderm/ectoderm-derived angiogenic cells. The arteries arise from the combination of the ectoderm (cells from the neural crests) and the mesoderm (pharyngeal mesoderm).
The first arteries that develop are the right and left primitive aortae, which are a continuation of endocardial cardiac tubes. These primitive aortae curve posteriorly in the first pharyngeal arch, around the anterior part of foregut and then continue posteriorly as two dorsal aortae. These two aortae also fuse cranially close to the heart, forming the aortic sac. The aortic sac continues caudally as truncus arteriosus and lies ventral to the pharynx. The two dorsal aortae lie dorsal to the primitive gut and pass caudally and fuse at the distal end to form a common aorta while the cranial part remains separate.
The aortic sac and the two dorsal aortae connect ventrally with aortic arches that are six pairs of arteries. The aortic arches run in the pharyngeal arches along the pharyngeal wall. During the development of the pharyngeal arches, the aortic sac sends a pair of branches to each pharyngeal arch which curves around the pharynx in the corresponding pharyngeal arch and eventually ends in the dorsal aorta. This artery is called an aortic arch artery, and these six pairs of arteries are never present at the same time in an embryo; by the time the third pair develops, the first pair has regressed.
The aortic arches decrease in number and undergo rearrangement, and each arch then gives rise to a structure vital for adult life. The structures arising from the aortic arches are as follows:
First aortic arch: It regresses except for a very small part that gives rise to the maxillary artery.
Second aortic arch: It regresses except for a very small part giving rise to the stapedial artery.
Third aortic arch: This arch is the source of the common carotid artery and the proximal part of the internal carotid artery, and the external carotid which arises as a bud from this arch.
Right Fourth aortic arch: Is the genesis of the proximal part of the right subclavian artery.
Left Fourth aortic arch: Gives rise to the medial portion of the arch of the aorta.
Fifth aortic arch: The fifth aortic arch regresses completely and very early in the development.
Sixth aortic arch: Either of the sixth aortic arches divides into ventral and dorsal segments, and therefore, their derivatives also divide into these two segments.
The aortic sac has two horns; right and left.
Development of the Aortic Arch:
The arch of the aorta has origins from multiple structures. The part of the aortic arch proximal to the origin of the innominate artery is the proximal part of the aorta, and it arises from the stem of the aortic sac. The area between the innominate artery and the left common carotid is called the middle region of the aortic arch and develops from the left horn of the aortic sac. The part of the aortic arch distal to the left common carotid artery forms from the left fourth aortic arch and the lower part of the left dorsal aorta.
Both the dorsal aortae also give rise to seven cervical intersegmental arteries, and upper six of those anastomose vertically which eventually gives rise to the second part of the vertebral artery, superior intercostal artery, and the deep cervical artery. The last seventh segmental artery gives rise to the subclavian artery.
The Common Dorsal Aorta:
It forms when the right and left dorsal aorta merge at the level of fourth thoracic to fourth lumbar somite segment. It gives off several branches which later become blood supply to vital organs in the adult life:
Development of the arteries in the extremities:
Two types of vascular cells derive from mural cells. The first is the pericyte, which affects more small vessels, while the second type, vascular smooth muscle cells, are found, especially in large vessels. Pericytes play immune functions and can behave like stem cells. Vascular smooth muscle cells are involved in the function of vasoconstriction and vasodilation of the vessels (blood pressure and distribution of blood to the tissues). These cells also have the task of maintaining the morphology of the vessel.
Many molecules stimulate the maturation of mural cells (angiogenic factors and cytokines). For example, fibroblast growth factor (FGF) and beta-FGF, transforming growth factor of alpha type (TGF-alpha), angiogenin, interleukin type 8 (IL-8), angiopoietins.
Bone morphogenetic protein (BMP), Notch (receptor affine to integrin proteins) and Gata (transcription factors) families, T-box (a group of transcription factors); myocardin, semaphorin family are protein molecules capable of inducing a correct embryological development of the aortic arch.
Hoxa3 is a protein-coding gene involved in the regulation of the third pharyngeal arch, which molecule comes from the neural crests. This molecule conditions the physiological development of the carotid artery system.
There was an article on genetic tests published by several groups dealing with cardiac and arterial diseases: European Society of Cardiology Working Group of Grown-Up Congenital Heart Disease, the European Society of Cardiology the European Society of Human Genetics. Genetic testing could help prevent diseases and provide adequate treatment in clinical practice in the near future. Further advances in research are necessary before endorsing genetic testing as a first approach for human embryological assessment.
Notch pathway is essential for the construction of the aorta and aortic arch. We know several receptors like Notch1–4, and the related ligands (Jagged1–2, Delta-like1-4); these molecules are found on the surface of the cell and are defined as transmembrane proteins. The activation of these molecules produces a cascade of metabolic reactions that come to influence DNA. Alagille syndrome is a complex pathology, which carries links to an alteration of Jagged's response1; the disease alters, among other pathological signs, the function and morphology of large vessels.
A new protein-coding, the HECTD1 ubiquitin ligase, has been shown to be essential in the development of the aortic arch, influencing the function of retinoic acid. Its functional alteration causes hypoplasia or pathological changes of the aortic arch.
Inosine 5 'monophosphate dehydrogenase (IMPDH) of type 2, deriving from the neural crests is fundamental for the development of large vessels. Its importance derives from its ability to influence the guanine nucleotide synthesis correctly; its dysfunction causes aberrations of the large vessels.
In the Human Gene Mutation Database, it is possible to find all the mutations known about humans and large vessels.
The in-depth and thorough knowledge regarding the embryological origin and evolution in adulthood is pivotal in understanding the pathophysiology of various congenital and acquired anomalies and enables physicians to initiate the treatment in the most accurate fashion. Integration of embryology in the medical curricula with the assistance of cutting-edge technology is also essential as it is associated with better patient outcomes.
|||EDWARDS JE, Anomalies of the derivatives of the aortic arch system. The Medical clinics of North America. 1948 Jul [PubMed PMID: 18877614]|
|||Türkvatan A,Büyükbayraktar FG,Olçer T,Cumhur T, Congenital anomalies of the aortic arch: evaluation with the use of multidetector computed tomography. Korean journal of radiology. 2009 Mar-Apr [PubMed PMID: 19270864]|
|||Onwuka E,King N,Heuer E,Breuer C, The Heart and Great Vessels. Cold Spring Harbor perspectives in medicine. 2018 Mar 1 [PubMed PMID: 28289246]|
|||VANMIEROP LH,ALLEY RD,KAUSEL HW,STRANAHAN A, PATHOGENESIS OF TRANSPOSITION COMPLEXES. I. EMBRYOLOGY OF THE VENTRICLES AND GREAT ARTERIES. The American journal of cardiology. 1963 Aug [PubMed PMID: 14047494]|
|||Cantador AA,Siqueira DED,Guillaumon AT, Anomaly in the Embryogenesis of the Aorta associated with Subclavian Steal Phenomenon. Annals of vascular surgery. 2019 Jun 11 [PubMed PMID: 31200064]|
|||Bhatia A,Bordoni B, Embryology, Gastrointestinal . 2019 Jan [PubMed PMID: 30725857]|
|||[PubMed PMID: 27504274]|
|||[PubMed PMID: 27473223]|
|||[PubMed PMID: 31194331]|
|||[PubMed PMID: 30615476]|