Embryology, Bowel

Development

Gastrulation is a process that occurs early in development and forms the three primary germ layers: endoderm, mesoderm, and ectoderm.[2] The gastrointestinal tract derives from these layers, and each layer contributes to a specific role in the mature intestine. The endoderm forms the innermost layer of the bowel, which is the epithelial layer of the intestinal mucosa. The mesoderm forms the muscular layer and the lamina propria. The ectoderm creates the enteric nervous system which develops from neural crest cells.[3]

Early in the formation of the primitive gut tube, the endodermal layer recruits the splanchnopleure mesoderm which goes on to become the bowel mesentery, connecting the gut tube posteriorly in the embryo.[4] By week four of development, the division of the gastrointestinal tract into the foregut, midgut, and hindgut has occurred.[5] 

The small and large intestines undergo rapid growth during weeks four and five of development. Embryological science believes that the enlarging intestines quickly outgrow the space available in the abdominal cavity causing the entire midgut to herniate into the umbilical cord forming a loop. The superior limb of the intestinal loop forms the ileum while the inferior limb forms the colon. Between the two limbs is the vitelline duct which connects the intestine to the yolk sac. From here, the bowel continues to grow and rotate for the next five weeks as follows:

• The herniated intestine rotates ninety degrees counterclockwise around the mesentery causing the proximal portion of the loop to migrate from the superior position to the right side and the distal portion of the loop to migrate from the inferior position to the left.
• At week ten, the bowel retracts back into the abdominal cavity where it rotates one hundred and eighty degrees more counterclockwise. The cecum is now in the right upper quadrant of the abdominal cavity.
• Enlargement of the large intestine pushes the cecum down into its final position in the right lower quadrant.[4]

During the time of midgut growth and rotation, other developmental changes are occurring simultaneously, including[6][7][6]:

• Week 4: Neural crest cells enter the foregut.
• Week 7: Neural crest cells reach the hindgut.
• Week 9: The cloaca becomes patent, and villus formation begins.
• Weeks 11: Mature smooth muscle layers are present along the gastrointestinal tract.

Cellular

The enteric nervous system (ENS), which allows for intrinsic innervation of the gastrointestinal tract derives from neural crest cells. The enteric nervous system has two ganglion plexus layers: the myenteric plexus, which occupies a position between the circular and longitudinal muscles and the submucosal plexus. The development of the ENS begins at week four of development when neural crest cells develop in the foregut. These cells then migrate distally and reach the hindgut around week seven. Smooth muscle in the gastrointestinal tract also matured in a proximal to distal fashion starting at week eight and concluding around week eleven. Interstitial cells of Cajal, which serve as the pacemaker cells of the ENS, are found in the bowel wall by eleven weeks.[6]

The gastrointestinal epithelium is also changing during this time from simple epithelium to a thick, pseudostratified epithelium that nearly occludes the lumen. The epithelium then becomes stratified and secondary lumina for throughout the epithelium. These secondary lumina fuse to form a continuous lumen creating a patent gastrointestinal tract, and the epithelium reorganizes into the simple columnar epithelium. Villi also begin to form from mesenchyme that pushes through pushes into the epithelium. The development of crypts, which are the site of stem cells, Paneth cells, and goblet cells, follows villi formation when endoderm invaginates into the mesodermal layer.[2]

Lgr5 + stem cells (leucine-rich repeat-containing G-protein coupled receptor 5) develop during the growth of intestinal villi and crypts and are essential for the biochemical balance of the intestine. These stem cells are also present in the formed intestine.

Biochemical

The bowel movement during the ontogenetic process occurs by the concomitant intervention of the enteric system development. This combination is made possible by the presence of embryonic nitric oxide (NO). Its deficiency (NO) causes a decrease in intestinal amplitude and contractile frequency and reduced response to cholinergic, including adrenergic and non-adrenergic non-cholinergic (NANC) stimuli (ATP, GABA, dopamine, neuropeptide Y, vasoactive intestinal peptide, and other molecules).

Molecular Level

The development of the bowel is a complex process that relies on many signaling mechanisms. There are also many genes required to induce anterior-posterior patterning, which causes differentiation of the foregut, midgut, and hindgut structures. The NODAL gene induces expression of specific transcription factors at different points in the gastrointestinal tract including the anterior (rostral) expression of Hhex, FoxA2, and Sox2 and posterior (caudal) expression of Cdx2 and Wnt. These differences are responsible for the difference in the intestinal epithelium from proximal to distal. These genes must be active during gastrulation to have proper development of the gastrointestinal tract.[2]

Intestinal villi are stimulated to develop by crosstalk between the endoderm and mesenchyme. Hedgehog signals from Shh and Ihh are essential in the development of the mesenchyme as well as promoting villus formation. Mesenchyme expresses BMPs and PDGFR-alpha to stimulate villus emergency and Sox9 in intervillous areas, restricting villi formation in these locations.[2]

Function

The primary function of the bowel is to absorb nutrients from the diet. It also has a role in the endocrine system and the immune system.

Testing

Detecting errors in bowel formation may occur in-utero in cases such as intestinal atresia or omphalocele, during the early postnatal period in cases such as Hirschsprung disease or may go undetected in cases such as malrotation. Prenatal ultrasound can detect polyhydramnios, which is a condition that can occur when the fetal gastrointestinal tract does not process the amniotic fluid produced by the fetal kidneys.[1] Duodenal atresia impedes the passage of amniotic fluid, causing polyhydramnios. Other signs of duodenal atresia detected on prenatal ultrasound include distention of the stomach and proximal duodenum, termed the double bubble sign. Fetal MRI can confirm this finding and can also discover more distal small bowel atresia. Another abnormality detectable in the fetal period by using fetal MRI is anal atresia, although it is more commonly found postnatally when there is a failure to pass meconium.[8] Omphalocele often turns up during routine prenatal ultrasound as well as elevated maternal serum alpha-fetoprotein concentration.[9] Hirschsprung disease most commonly presents after birth with failure to pass meconium and diagnosis can be confirmed with a suction rectal biopsy.[10] 

Pathophysiology

The complexity of bowel formation allows for many areas in which there can be errors in development. These errors manifest as the following diseases[11][12][9][13]:

• Malrotation - the midgut does not undergo proper rotation which predisposes to midgut volvulus.
• Volvulus - bowel twists around its mesentery, causing bowel obstruction.
• Persistent Vitelline Duct - the vitelline duct connection to the umbilicus remains patent resulting in enteric drainage.
• Meckel Diverticulum - this condition is a remnant of the vitelline duct attached by a fibrous stalk to the umbilicus, which can cause bowel obstruction or bleeding if ectopic gastric tissue is present in the diverticulum.
• Omphalocele - This represents a failure of the herniated midgut to return to the abdominal cavity.
• Hirschsprung Disease  - this is the failure of neural crest cell migration, which impairs relaxation of the bowel, creating an obstruction.
• Imperforate Anus - the cloaca fails to perforate, and thus the rectum leads into a blind pouch.
• Intestinal Atresia - discontinuous bowel thought to be due to disruptions in a segment of bowel blood flow
• Gastrointestinal duplications are very rare pathologies, with a response in the population of 4 to 18% regarding the colon. It is not always readily identifiable in the pediatric period, with symptoms such as colic and constipation.

Clinical Significance

Bowel embryology is a complex process that depends on proper signaling from many transcription factors to have proper growth, rotation, and functional epithelium with villi. Understanding the normal sequence of events is important as the basis for many congenital gastrointestinal diseases are a result of errors in this process.