Title: Development of the Urogenital System
1Development of theUrogenital System
- Montakarn Tansatit, M.D.
- Department of Anatomy
- Faculty of Medicine
- Chulalongkorn University
2Urogenital system
- develops from intermediate mesoderm
- Urogenital ridge
- Nephrogenic cord urinary system
- Gonadal (genital) ridge genital system
3Developmentof theUrinary System
4Urinary system
- intermediate mesoderm ? urogenital ridge
- Part of the urogenital ridge forms the
nephrogenic cord - Nephrogenic cord develops into three sets of
nephric structures - 1. Pronephros
- 2. Mesonephros
- 3. Metanephros
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6Kidneys
- Three sets of excretory organs develop in human
embryos - 1. Pronephros
- 2. Mesonephros
- 3. Metanephros
7Pronephros
- is the cranialmost nephric structure
- pronephric tubules and pronephric duct
- is a transitory structure that regresses
completely by week 5 of development and is not
funcitonal in humans
8Mesonephros
- is the middle nephric structure
- mesonephric tubules and mesonephric duct
(wolffian duct) - is partially transitory and is functional for a
short period
9Mesonephros
- most of the mesonephric tubules regress, but the
mesonephric duct persists and opens into the
urogenital sinus - mesonephroi degenerate by the end of the first
trimester
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12Metanephros
- develops from an outgrowth of the mesonephric
duct, the ureteric bud, and from a condensation
of mesoderm within the nephrogenic cord, the
metanephric blastema - is the caudalmost nephric structure
13Metanephros
- begins to form at week 5 and is functional in the
fetus at about week 10 of development - develops into the definitive adult kidney
14Development of the kidneys
- Ureteric bud
- Ureters
- Renal pelvis
- Major calyces
- Minor calyces
- Collecting tubules
15Development of the kidneys
- The inductive influence of the collecting
tubules causes the formation of metanephric
vesicles
16Nephron formation
- The metanephric vesicles differentiate into
- Distal tubule
- Loop of Henle
- Proximal tubule
- Bowmans capsule
17Uriniferous tubule
- consists of two embryologically different parts
- 1. Nephron is derived from the metanephric mass
of mesoderm - 2. Collecting tubule is derived from the
ureteric bud (metanephric diverticulum)
18Nephron formation
- is complete at birth, but functional maturation
of nephrons continues throughout infancy
19Fetal kidney
- The fetal kidneys are subdivided into lobes that
are visible externally - The lobulation disappears during infancy and is
obscured in definitive adult kidney
20Positional changes of the kidneys
- Initially permanent kidneys lie close to each
other in the pelvis - gradually come to lie in the abdomen and move
farther apart - attain their adult position by the ninth week
- as the kidneys ascend they rotate medially almost
90 degrees
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22Anomalies of the Kidney
23Renal agenesis
- ureteric bud fails to develop
- 1. Unilateral renal agenesis
- 2. Bilateral renal agenesis
24Unilateral renal agenesis
- is relatively common
- occurs about 1 in every 1,000 newborn infants
- is more common in males
- is asymptomatic
- should be suspected in infants with a single
umbilical artery
25Bilateral renal agenesis
- is associated with oligohydramnios
- occurs about 1 in 3,000 births
- is incompatible with life
26Horseshoe kidney
- 1 in about 500 persons
- 7 of persons with Turner syndrome
- is asymptomatic
27Development of the urinary bladder
- Division of the cloaca by the urorectal septum
into - urogenital sinus ventrally
- rectum dorsally
28Urogenital sinus
- Vesical part - continuous with the allantois
- Pelvic part - becomes the bladder neck, prostatic
part of urethra in male and entire female urethra - Phallic part - grows toward the genital tubercle
29Development of the urinary bladder
- is formed from the upper end of the urogenital
sinus (vesical part) which is continuous with the
allantois - The allantois becomes a fibrous cord, the urachus
(median umbilical ligament in adult)
30Anomaliesof theUrinary Bladder
31Extrophy of the bladder
- occurs about 1 in every 10,000 to 40,000 births
- the posterior wall of the urinary bladder is
exposed to the exterior - is caused by a failure of the anterior abdominal
wall and anterior wall of the bladder to develop
properly
32Extrophy of the bladder
- is associated with urine drainage to the exterior
and epispadias
33Urachal cyst or sinus
- a remnant of the allantois persists
- is found along the midline on a part from the
umbilicus to the apex of the urinary bladder - is often associated clinically with urine
drainage from the umbilicus
34Development of the urethra
- Epithelium is derived from endoderm of the
urogenital sinus - distal part of the urethra in male is derived
from the glandular (urethral) plate
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36Developmentof theReproductive System
37Reproductive System
38Indifferent stage
- The initial period of genital development which
the early genital system in the two sexes are
similar.
39- Phenotypic sexual differentiation may result in
individuals with - Female phenotype
- Intersex phenotype
- Male phenotype
40- The components of the indifferent embryo that
are remodeled to form the adult female or male
reproductive systems are - 1. Gonads
- 2. Genital duct systems
- 3. Primordium of the external genitalia
41Gonads
- The indifferent embryo has one pair of gonads
that develop into either the ovaries or testes - The gonads are derived from three sources
- mesothelium
- underlying mesenchyme
- primordial germ cells
42Indifferent gonads
- Gonadal (genital) ridge
- primary sex cords grow into the underlying
mesenchyme - consist of
- cortex
- medulla
43Indifferent gonads
44Primordial germ cells
- Primitive sex cells
- are among the endodermal cells of the yolk sac
near the origin of the allantois - migrate along the dorsal mesentery of the hindgut
to the gonadal ridge and enter the underlying
mesenchyme
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47Genital duct systems
- The indifferent embryo has 2 separate genital
duct systems - 1. Paramesonephric (Mullerian) ducts
- play a major role in the female
- 2. Mesonephric tubules and mesonephric (Wolffian)
ducts - play a major role in the male
48Primordium of the external genitalia
- The indifferent embryo has one primordium of
the external genitalia, which will differentiate
along either female or male lines
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50Sex determination
- SRY gene on short arm of chromosome Y
- Testis-determining factor (TDF)
- Two X chromosome are required for the development
of the female phenotype
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52Developmentof theFemale Reproductive System
53Gonad
- Intermediate mesoderm ? urogenital ridge ?
gonadal ridge - primary sex cords ? rete ovarii ? degenerate
- secondary sex cords ? primordial follicles
(contain oogonium)
54Ovary
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56Oogenesis
- Primordial germ cells ? oogonium
- active mitosis of oogonia occurs during fetal
life - no oogonia form posnatally
57Genital duct systems
- Paramesonephric ducts
- uterine tubes
- hydatid of Morgagni
- uterovaginal primordium
- uterus
- cervix
- superior third of the vagina
58Development of the uterus
59Uterus
- Paramesonephric ducts
- unfused cranial parts uterine tubes
- fused caudal parts uterovaginal primordium
60Development of the vagina
61Vagina
- Sinovaginal bulbs fuse to form a vaginal plate
62Development of the vagina
- Endoderm of urogenital sinus vaginal epithelium
- Surrounding mesenchyme fibromuscular wall
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67Genital duct systems
- Mesonephric tubules and ducts
- regress completely in the female after formation
of the metanephric kidney - vestigial remnants persist as the
- appendix vesiculosa
- epoophoron
- paroophoron
- Gartners duct
68Primordium of the external genitalia
- Genital tubercle ? phallus
- Urethral folds
- Genital swelling
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71Primordium of the external genitalia
72Developmentof theMale Reproductive System
73Gonad
- Intermediate mesoderm ? urogenital ridge ?
gonadal ridge - Testes determining factor (TDF) (on Y chromosome)
- primary sex cords containing primordial germ
cells (XY genotype)
74Testes
- TDF induces the primary sex cord to condense and
extend into the medulla of the indifferent gonad - The development of the dense tunica albuginea is
the characteristic and diagnostic feature of
testicular development
75Testes
- Primary sex cords
- seminiferous cords
- tubuli recti
- rete testes
- Seminiferous cords are made up of spermatogonia
and Sertoli cells secrete mullerian-inhibiting
factor (MIF)
76Seminiferous tubules
- Sertoli cells are derived from the surface
epithelium of the testes - Spermatogonia are derived from the primordial
germ cells
77Testes
- The mesoderm between the seminiferous cords gives
rise to the interstitial (Leydig) cells, which
secrete testosterone - Seminiferous cords remain as solid cords until
puberty when they acquire a lumen and are then
called seminiferous tubules
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79Testes
- Sertoli cells begin producing mullerian
inhibiting substance at 6-7 weeks - Interstitial cells begin producing testosterone
in 8th week - Testosterone production is stimulated by hCG
80Descent of the testes
- is associated with
- Enlargement of the testes and atrophy of the
mesonephroi - Atrophy of the paramesonephric ducts
- Enlargement of the processus vaginalis
812 months
82After birth
83Genital duct systems
- Paramesonephric ducts
- Under the influence of MIF, the cranial portions
of the paramesonephric ducts and the uterovaginal
primordium regress completely - A vestigial remnant may persist the appendix
testis
84Genital duct systems
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86Primordium of the external genitalia
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88Intersexuality (Hermaphroditism)
- True intersexuality
- Female pseudointersexuality
- Male pseudointersexuality
89True intersexuality
- has both ovarian and testicular tissue
(ovotestes) - ambiguous genitalia
- usually have a 46,XX genotype (70)
90Female pseudointersexuality
- has only ovarian tissue histologically
- masculinization of the female external genitalia
- have a 46,XX genotype
- most common cause is
- congenital adrenal hyperplasia (excess androgens)
91Congenital adrenal hyperplasia(CAH)
- Excessive androgen production during fetal period
- causes masculinization of the external genitalia
and enlargement of the clitoris in females
92Congenital adrenal hyperplasia(CAH)
- autosomal recessive disorders
- mutation in cytochrome P450c21-steroid
21-hydroxylase gene
93Male pseudointersexuality
- has only testicular tissue histologically
- various stages of stunted development of the male
external genitalia - have a 46,XY genotype
- most common cause is
- inadequate production of testosterone and MIF by
the fetal testes
94Androgen insensitivity syndrome(AIS)
- Testicular feminization syndrome
- 1 in 20,000 live births
- are normal-appearing females
- 46,XY genotype
- testes are present
- results from a defect in the androgen receptor
mechanism
95Hypospadias
- Most common anomaly of the penis
- 1 in every 300 male infants
- there are 4 types
- glandular hypospadias
- penile hypospadias
- penoscrotal hypospadias
- perineal hypospadias
80 of cases
96Cryptorchidism(undescended testes)
- 30 of premature males 3-4 of full-term males
- failure of development and atrophy are detectable
by the end of the first year - may result from deficiency of androgen production
97The End