Difference between revisions of "Sexual Differentiation - Anatomy & Physiology"
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− | + | {{toplink | |
+ | |backcolour =EED2EE | ||
+ | |linkpage =Reproductive System - Anatomy & Physiology | ||
+ | |linktext =Reproductive System | ||
+ | |maplink = Reproductive System (Content Map) - Anatomy & Physiology | ||
+ | |pagetype =Anatomy | ||
+ | |sublink1=Reproductive System - Anatomy & Physiology#Fertilisation.2C Implantation and Early Embryonic Development | ||
+ | |subtext1=FERTILISATION , IMPLANTATION AND EARLY EMBRYONIC DEVELOPMENT | ||
+ | }} | ||
+ | <br> | ||
[[Image:Overview of Sexual Differentiation.jpg|thumb|right|150px|Overview of Sexual Differentiation,Copyright RVC 2008]] | [[Image:Overview of Sexual Differentiation.jpg|thumb|right|150px|Overview of Sexual Differentiation,Copyright RVC 2008]] | ||
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* Sex cord cells proliferate to form the testes cord. During this period '''SRY''' is expressed for the first time within '''Sertoli cells''' (SRY is NOT expressed in primordial germ cells). | * Sex cord cells proliferate to form the testes cord. During this period '''SRY''' is expressed for the first time within '''Sertoli cells''' (SRY is NOT expressed in primordial germ cells). | ||
− | * Sex cords with a basement membrane become '''semniferous | + | * Sex cords with a basement membrane become '''semniferous Cords''' which give rise to '''semniferous Tubules'''. |
* '''Within the semniferous cords''' are two cell populations: | * '''Within the semniferous cords''' are two cell populations: | ||
** '''Primordial germ cells''' - Prospermatogonia which give rise to '''spermatozoa''' | ** '''Primordial germ cells''' - Prospermatogonia which give rise to '''spermatozoa''' | ||
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* '''Between cords''', the loose mesenchyme undergoes '''vascularisation''' and develops as '''stromal tissue'''. | * '''Between cords''', the loose mesenchyme undergoes '''vascularisation''' and develops as '''stromal tissue'''. | ||
* Within the stromal tissue, cells condense into clusters to form specialized endocrine units - the interstitial '''Leydig's cells''' | * Within the stromal tissue, cells condense into clusters to form specialized endocrine units - the interstitial '''Leydig's cells''' | ||
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== Female == | == Female == | ||
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* In absence of these testicular hormones, female differentiation occurs. | * In absence of these testicular hormones, female differentiation occurs. | ||
* Thus, sexual differentiation must be actively diverted down the male route, the female route requires no active intervention. | * Thus, sexual differentiation must be actively diverted down the male route, the female route requires no active intervention. | ||
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Revision as of 14:47, 13 August 2009
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Genetic Sex
- Established at the time of fertilisation.
- The foetus receives its genetic endowment in two equal portions from the male gamete (spermatozoon) and female gamete (oocyte).
- The X sex chromosome is larger than the Y sex chromosome.
- Females have XX chromosomes. All oocytes contain one X chromosome, they are the homogametic sex.
- Males have XY chromosomes. Spermatozoa form two distinct populations, one containing X chromosomes and one containing Y chromosomes. They are the heterogametic sex.
- The Y chromosome is required to initiate male development.
- In absence of the Y chromosome, female gonads (ovaries) will develop.
- The prime male determining gene is SRY (sex determining region of the Y chromosome).
- SRY is a very small piece of DNA that acts as a molecular switch to regulate structural genes and autosomal chromosomes, determining if and when they are to be activated.
- SRY encodes the protein Testes Determining Factor (TDF)
- The presence of SRY alone is sufficient to ensure development of male gonads (testes).
- Female is the default sex, in absence of SRY female gonads (ovaries) will develop.
- Subsequent gonadal development is dependent on a normal population of germ cells.
- Normal oocyte growth requires the activity of both X chromosomes.
- Normal spermatogenesis requires the activity of no more than one X chromosome.
- Early development of gonads proceeds similarly in both sexes. The gonads are derived from two distinct tissues:
- Somatic mesenchymal tissue forms the matrix of the gonad
- Primordial germ cells form the gametes
- Genital ridge forms from somatic mesenchyme.
- Primordial germ cells migrate to the genital ridge.
- At this stage it is not possible to discriminate between male and female gonads.
- Y chromosomal determination of gonadal sex is only visible when primordial germ cell colonisation is complete.
Male
- Sex cord cells proliferate to form the testes cord. During this period SRY is expressed for the first time within Sertoli cells (SRY is NOT expressed in primordial germ cells).
- Sex cords with a basement membrane become semniferous Cords which give rise to semniferous Tubules.
- Within the semniferous cords are two cell populations:
- Primordial germ cells - Prospermatogonia which give rise to spermatozoa
- Mesodermal cord cells which give rise to Sertoli cells
- Between cords, the loose mesenchyme undergoes vascularisation and develops as stromal tissue.
- Within the stromal tissue, cells condense into clusters to form specialized endocrine units - the interstitial Leydig's cells
Female
- At the time the male gonad is undergoing marked changes under the direction of SRY, the female gonad continues to appear indifferent and does not express SRY.
- Small clusters of mesenchyme surround the germ cells to initiate formation of primary follicles, characteristic of the ovary.
- In follicles
- Mesenchymal cells give rise to granulosa cells
- Germ cells give rise to oocytes
Foetal sex differentiation
- Endocrine activity of the ovaries is NOT essential for sex differentiation during foetal life, abnormal ovarian development will have no effect until puberty.
- Testes secrete two essential hormones:
- Steroidal hormones (mainly C19 androgens) from leydig's cells
- Mullarian Inhibiting Hormone (MIH) also known as Anti-Mullarian Hormone (AMH) from Sertoli cells
- In absence of these testicular hormones, female differentiation occurs.
- Thus, sexual differentiation must be actively diverted down the male route, the female route requires no active intervention.