– Derived from a dorsal evagination of the ectoderm of the oropharynx (stomodeum) toward the brain (Rathke’s pouch); eventually meets and partially surrounds neurohypophysis
Neurohypophysis
– Derived from a downgrowth (the future infundibulum) of neuroectoderm of the floor of the third ventricle (diencephalon); pituicytes differentiate from infundibular cells
Pituitary Abnormalities
: Rare; most common is missing pituitary
(2) Hypothalamus
(4th week) – from ectoderm
floor of diencephalon immediately cranial to infundibulum thickens, folds back caudally and finally comes to lie just dorsal to (on top of) the infundibulum
nerve fibers of hypothalamic neurons grow into infundibulum and terminate in the capillary beds of the pars nervosa
late in the fetal period cytodifferentiation occurs and small amounts of hormone are produced
(3) Pineal Gland
(7th-8th week) – from ectoderm
develops from neuroectoderm of posterior portion of roof of diencephalon–remains attached to brain by a short stalk
the pineal gland is the ephysis of the diencephalon
Does not have photoreceptors in people; function is to secrete melatonin, which controls circadian rhythms
(4) Adrenal Glands
(5th-6th week) – from mesoderm and ectoderm
Cortex
– derived from mesodermal mesenchyme lining posterior abdominal wall medial to genital ridge and lateral to dorsal mesentary
fetal cortex
(inner mass of cells) functions during fetal period but degenerates soon after birth
produces D -5,3-b -hydroxy steroids (100-200 mg/day)
differentiation of permanent cortex (outer mass of cells) begins during late fetal period
Zona glomerulosa
and fasciculata are present at birth; Zona reticularis appears near end of 3rd year after birth.
Medulla
– neuroectodermal cells migrate from the neural crest of the trunk region into the region of celiac ganglia and on to the developing suprarenal cortex – these cells populate the central region of the gland
this migration continues to birth
epinephrine and norepinephrine are produced and secreted by different cell types
epinephrine
by cells with small granules
norepinephrine
by cells with large granules
(5) Thyroid (24th day) – from endoderm (except parafollilular cells (C cells), from neural crest)
develops from foramen cecum – endoderm in midline of floor of pharynx between 1st and 2nd pharyngel pouches, just caudal to median tongue bud
foramen cecum thickens to form unpaired thyroid primordium that elongates and invaginates Þ thyroid diverticulum
diverticulum continues to grow caudally, becomes thyroglossal duct; tip expands and bifurcates to form thyroid Þ two thyroid lobes connected by isthmus
thyroglossal duct connects the gland with its site of origin (the foramen cecum) at the base of the tongue
by 7th week, duct has regressed; however, distal part persists in 50% of people as the pyramidal lobe of the thyroid
Follicular Cells
– secrete T4 and T3, arise from a downward growth of endodermal epithelium
by 10th week contain colloid
by 12th-13th week synthesize non-iodinated thyroglobulin
by 16th week synthesize T3
Parafollicular Cells
(C cells) – secrete calcitonin, arise from neural crest cells (ultimobranchial (telopharyngeal) bodies) that migrate into the developing thyroid gland
Thyroid Abnormalities
: Many, since it migrates from place of origin; can have thyroid tissue from back of tongue down
(6) Parathyroid Gland
(5th week) – from ectoderm
inferior parathyroid glands and thymus derive from 3rd branchial pouch; superior parathyroid glands derive from 4th
normally, the inferior parathyroids separate from the thymus and come to lie below the superior parathyroids
start producing PTH by 7th week (when bones start ossifying)
oxyphil cells appear a few years before puberty
(7) Pancreas (Islets of Langerhans)
(10th-11th week) – from endoderm
dorsal and ventral pancreatic buds rotate and fuse to create pancreas
the islets bud off the pancreatic duct system and form clusters of endocrine cells; alpha, then beta, then delta
insulin
appears in the 10th week and glucagon by the 15th week
Pancreatic Abnormalities
:
missing
strangulation of duodenum because of malrotation of dorsal pancreatic bud