Spermatogonium

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Spermatogonium [1]
Germinal epithelium testicle.svg
Germinal epithelium of the testicle. 1 basal lamina, 2 spermatogonia, 3 spermatocyte 1st order, 4 spermatocyte 2nd order, 5 spermatid, 6 mature spermatid, 7 Sertoli cell, 8 tight junction (blood testis barrier)
Testicle-histology-boar.jpg
Histological section through testicular parenchyma of a boar. 1 Lumen of Tubulus seminiferus contortus, 2 spermatids, 3 spermatocytes, 4 spermatogonia, 5 Sertoli cell, 6 myofibroblasts, 7 Leydig cells, 8 capillaries
Identifiers
MeSH D013093
FMA 72291
Anatomical terminology

A spermatogonium (plural: spermatogonia) is an undifferentiated male germ cell. Spermatogonia undergo spermatogenesis to form mature spermatozoa in the seminiferous tubules of the testicles.

Contents

There are three subtypes of spermatogonia in humans:

Type A (dark) cells, with dark nuclei. These cells are reserve spermatogonial stem cells which do not usually undergo active mitosis. Type A (pale) cells, with pale nuclei. These are the spermatogonial stem cells that undergo active mitosis. These cells divide to produce Type B cells. Type B cells, which undergo growth and become primary spermatocytes.

Types of spermatogonia

Spermatogonia are often classified into different types depending on their stage in the differentiation process. In humans and most mammals, spermatogonia are divided into two types, A and B, but this can differ for other organisms. [2]

There are three subtypes of spermatogonia in humans:

Spermatogenesis

Spermatogenesis is the process in which sperm cells are produced and formed into mature spermatozoa from spermatogonia. Males mature spermatozoa (sperm) are produced to later join with a female oocyte (egg) to create offspring. Throughout the process of spermatogenesis, there are many different parts of the male anatomy, accessory organs, and hormones. However, spermatogenesis can be broken down in the following steps, which are initiated at the start of puberty:

Male hormones

Spermatogenesis is a very regulated process controlled by endocrine stimuli. These stimuli include the follicle-stimulating hormone (FSH) and the luteinizing hormone (LH), which stimulate testosterone. These hormones produce regulatory signals that control the maintenance and nutrients needed for the developing germ cells. The following explains what each hormone contributes to the regulation of spermatogenesis.

Sperm structure

The overall structure of spermatozoa is very specialized as the cell has fully differentiated and matured. As spermatozoa, the cell no longer undergoes division. It consists of a head, midpiece, and flagella tail for motility.  

Infertility

Infertility is the inability of a couple to conceive an offspring after a year of unprotected intercourse. Spermatogonia plays a vital role in male fertility, as they are the initial germ cells for sperm production. A disruption of spermatogonia’s function, structure, or development can lead to infertility. There are several factors that can affect spermatogenesis and the health of spermatogonia, including genetic disorders, hormonal imbalances, environmental factors, and many more. [7]  

Diseases That Cause Infertility

There are many diseases and causes of infertility experienced in males.

Cystic Fibrosis and Klinefelter's Syndrome are just two examples of ways diseases and genetic mutations can lead to infertility in men.

Anticancer drugs

Anticancer drugs such as doxorubicin and vincristine can adversely affect male fertility by damaging the DNA of proliferative spermatogonial stem cells. Experimental exposure of rat undifferentiated spermatogonia to doxorubicin and vincristine indicated that these cells are able to respond to DNA damage by increasing their expression of DNA repair genes, and that this response likely partially prevents DNA break accumulation. [11] In addition to a DNA repair response, exposure of spermatogonia to doxorubicin can also induce programmed cell death (apoptosis). [12]

Additional images

See also

References

  1. Mahla, R.S. (2012). "Spermatogonial Stem Cells (SSCs) in Buffalo (Bubalus bubalis) Testis". PLOS ONE. 7 (4): e36020. Bibcode:2012PLoSO...736020M. doi: 10.1371/journal.pone.0036020 . PMC   3334991 . PMID   22536454.
  2. Waheeb, R.; Hofmann, M.-C. (August 2011). "Human spermatogonial stem cells: a possible origin for spermatocytic seminoma". International Journal of Andrology. 34 (4 Pt 2): e296–305, discussion e305. doi:10.1111/j.1365-2605.2011.01199.x. ISSN   1365-2605. PMC   3146023 . PMID   21790653.
  3. 1 2 3 4 "Spermatogenesis". Default. Retrieved 2024-12-04.
  4. 1 2 3 4 5 6 7 8 Sharma, Rakesh; Agarwal, Ashok (2011), Zini, Armand; Agarwal, Ashok (eds.), "Spermatogenesis: An Overview", Sperm Chromatin: Biological and Clinical Applications in Male Infertility and Assisted Reproduction, New York, NY: Springer, pp. 19–44, doi:10.1007/978-1-4419-6857-9_2, ISBN   978-1-4419-6857-9 , retrieved 2024-12-04
  5. Oduwole, Olayiwola O.; Peltoketo, Hellevi; Huhtaniemi, Ilpo T. (2018-12-14). "Role of Follicle-Stimulating Hormone in Spermatogenesis". Frontiers in Endocrinology. 9: 763. doi: 10.3389/fendo.2018.00763 . ISSN   1664-2392. PMC   6302021 . PMID   30619093.
  6. Suede, Samah H.; Malik, Ahmad; Sapra, Amit (2024), "Histology, Spermatogenesis", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID   31985935 , retrieved 2024-12-04
  7. Leslie, Stephen W.; Soon-Sutton, Taylor L.; Khan, Moien AB (2024), "Male Infertility", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID   32965929 , retrieved 2024-12-04
  8. "Cystic Fibrosis — What Is Cystic Fibrosis?". NHLBI, NIH. 2024-11-15. Retrieved 2024-12-04.
  9. Naz Khan, Farah; Mason, Kelly; H Roe, Andrea; Tangpricha, Vin (2022). "CF and male health: Sexual and reproductive health, hypogonadism, and fertility". Journal of Clinical & Translational Endocrinology. 27: 100288. doi:10.1016/j.jcte.2021.100288. PMC   8695349 . PMID   34987977.
  10. Hawksworth DJ, Szafran AA, Jordan PW, Dobs AS, Herati AS (2018). "Infertility in Patients With Klinefelter Syndrome: Optimal Timing for Sperm and Testicular Tissue Cryopreservation". Rev Urol. 20 (2): 56–62. doi:10.3909/riu0790 (inactive 17 December 2024). PMC   6168324 . PMID   30288141.{{cite journal}}: CS1 maint: DOI inactive as of December 2024 (link)
  11. Beaud H, van Pelt A, Delbes G (2017). "Doxorubicin and vincristine affect undifferentiated rat spermatogonia". Reproduction. 153 (6): 725–735. doi: 10.1530/REP-17-0005 . PMID   28258155.
  12. Habas K, Anderson D, Brinkworth MH (2017). "Germ cell responses to doxorubicin exposure in vitro" (PDF). Toxicol. Lett. 265: 70–76. doi:10.1016/j.toxlet.2016.11.016. hdl: 10454/10685 . PMID   27890809.