Mesonephric duct

(Redirected from Wolffian structures)

The mesonephric duct, also known as the Wolffian duct, archinephric duct, Leydig's duct or nephric duct, is a paired organ that develops in the early stages of embryonic development in humans and other mammals. It is an important structure that plays a critical role in the formation of male reproductive organs. The term Wolffian duct is named after Caspar Friedrich Wolff, a German physiologist and embryologist who first described it in his dissertation in 1759.[1]

Mesonephric duct
Urogenital sinus of female human embryo of eight and a half to nine weeks old
Details
Carnegie stage11
Days28
PrecursorIntermediate mesoderm
Gives rise toVasa deferentia, seminal vesicles, epididymides, Gartner's duct
Identifiers
Latinductus mesonephricus; ductus Wolffi
MeSHD014928
TEduct_by_E5.6.2.0.0.0.4 E5.6.2.0.0.0.4
Anatomical terminology

During embryonic development, the mesonephric duct form as a part of the urogenital system.[2]

Structure

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The mesonephric duct connects the primitive kidney, the mesonephros, to the cloaca. It also serves as the primordium for male urogenital structures including the epididymides, vasa deferentia, and seminal vesicles.

Development

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The mesonephric duct typically forms around the 3rd-4th week of pregnancy, before the paramesonephric duct (also known as the Müllerian duct).

In both males and females, the mesonephric duct develops into the trigone of urinary bladder, a part of the bladder wall, and also produces WNT9B, which is required for the elongation of the paramesonephric duct.[3]

Male

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In a male, it develops into a system of connected organs between the efferent ducts of the testis and the prostate, namely the epididymis, the vas deferens, and the seminal vesicle. The prostate forms from the urogenital sinus and the efferent ducts form from the mesonephric tubules.

For this, it is critical that the duct is exposed to testosterone during embryogenesis. Testosterone binds to and activates androgen receptor, affecting intracellular signals and modifying the expression of numerous genes.[4]

In a mature male, the function of this system is to store and mature sperm, and provide accessory semen fluid.

Female

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In a female, with the absence of anti-Müllerian hormone secretion by the Sertoli cells and subsequent Müllerian apoptosis, the mesonephric duct regresses, although inclusions may persist. The vestigial epoophoron arises from this duct. Also, lateral to the wall of the vagina, a Gartner's duct could develop as a remnant. Normal regression starts with the action of COUP-TFII in the Wolffian mesenchyme.[5]

The mesenchyme of the mesonephric duct is retained in female reproductive tissue after sexual differentiation. As the mesonephric duct regresses, they undergo significant chromatin remodeling and move to surround the paramesonephric duct. Cells from the Wolffian mesenchyme occur in a layer around the inner epithelium, where the Müllerian mesenchyme cells also reside. The two can be distinguished by their gene expression profile: cells derived from the Wolffian mesenchyme expresses AR, while those from the Müllerian mesenchyme expresses AMHR2. Both types of mesenchyme become smooth muscle and fibroblasts. They appear quite evenly mixed in the oviduct, but remain clearly separated the uterus, with the Wolffian mesenchyme settling in the mesometrial side.[6]

Additional images

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Diagrams to illustrate the changes in the cloaca in mammals during development. A, early embryonic stage, showing the cloaca receiving the urinary bladder, the rectum, and the mesonephric duct, as in the lower vertebrates. B, later stage, showing the beginning of the fold which divides the cloaca into a ventral urogenital sinus which receives the urinary bladder, mesonephric duct, and ureters, and into a dorsal part which receives the rectum. C, further progress of the fold, dividing the cloaca into urogenital sinus and rectum; the ureter has separated from the mesonephric duct and is shifting anteriorly. D, completion of the fold, showing complete separation of the cloaca into ventral urogenital sinus and dorsal rectum.

See also

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References

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  1. synd/2845 at Whonamedit?
  2. Du, Hongling; Taylor, Hugh S. (2015). "Development of the Genital System". Principles of Developmental Genetics. pp. 487–504. doi:10.1016/b978-0-12-405945-0.00027-2. ISBN 978-0-12-405945-0.
  3. Roly, Zahida Yesmin; Backhouse, Brendan; Cutting, Andrew; Tan, Tiong Yang; Sinclair, Andrew H.; Ayers, Katie L.; Major, Andrew T.; Smith, Craig A. (May 2018). "The cell biology and molecular genetics of Müllerian duct development". WIREs Developmental Biology. 7 (3) e310. doi:10.1002/wdev.310. PMID 29350886.
  4. Hannema, Sabine E.; Print, Cristin G.; Charnock-Jones, D. Stephen; Coleman, Nick; Hughes, Ieuan A. (2006). "Changes in gene expression during Wolffian duct development". Hormone Research. 65 (4): 200–209. doi:10.1159/000092408. PMID 16567946. ProQuest 1233606874.
  5. Zhao, F; Grimm, SA; Yao, HH (2020). "Molecular Actions Underlying Wolffian Duct Regression in Sexual Differentiation of Murine Reproductive Tracts". Sexual Development. 14 (1–6): 51–59. doi:10.1159/000513878. PMC 8328876. PMID 33684916.
  6. Zhao, F; Grimm, SA; Jia, S; Yao, HH (September 2022). "Contribution of the Wolffian duct mesenchyme to the formation of the female reproductive tract". PNAS Nexus. 1 (4) pgac182. doi:10.1093/pnasnexus/pgac182. PMC 9523451. PMID 36204418.
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Further reading

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