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Related Concept Videos

Sperm Structure and Semen Composition01:22

Sperm Structure and Semen Composition

During ejaculation, males release around 2-5 milliliters of semen, which is a complex mixture of mature sperm and various fluids produced by accessory glands. The mature sperm cells measure approximately 60 micrometers in length and consist of a head, neck, midpiece, and tail. The head is flattened and tapered, measuring about 4 to 5 micrometers in length. It contains a nucleus with condensed chromosomes and an acrosome, a cap-like structure filled with enzymes essential for penetrating the...
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Sperm Transport

The journey of sperm from its origin to the point of ejaculation begins within the seminiferous tubules of the testis. Here, Sertoli cells produce fluid that propels non-motile sperm through a series of conduits, starting with the straight tubules leading to the rete testis. This interconnected network of tubules acts as the initial pathway for sperm, guiding them into the efferent ductules and then into the epididymis for maturation.
The maturation phase occurs in the epididymis, where sperm...
Spermatogenesis01:41

Spermatogenesis

Spermatogenesis is the process by which haploid sperm cells are produced in the male testes. It starts with stem cells located close to the outer rim of seminiferous tubules. These spermatogonial stem cells divide asymmetrically to give rise to additional stem cells (meaning that these structures “self-renew”), as well as sperm progenitors, called spermatocytes. Importantly, this method of asymmetric mitotic division maintains a population of spermatogonial stem cells in the male reproductive...

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Related Experiment Video

Updated: May 16, 2026

Sperm Collection of Differential Quality Using Density Gradient Centrifugation
03:28

Sperm Collection of Differential Quality Using Density Gradient Centrifugation

Published on: November 29, 2018

Seminal plasma effects on sex-sorting bovine sperm.

C A Burroughs1, J K Graham, R W Lenz

  • 1Animal Reproduction and Biotechnology Laboratory, Colorado State University, Fort Collins, Colorado, USA.

Theriogenology
|December 19, 2012
PubMed
Summary

Removing seminal plasma from bovine sperm during flow cytometry sorting improved live-orientation and sort rates. Storing sperm without seminal plasma enhanced post-thaw motility, crucial for artificial insemination success.

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Last Updated: May 16, 2026

Sperm Collection of Differential Quality Using Density Gradient Centrifugation
03:28

Sperm Collection of Differential Quality Using Density Gradient Centrifugation

Published on: November 29, 2018

Collection of Post-mating Semen from the Female Reproductive Tract and Measurement of Semen Liquefaction in Mice
12:06

Collection of Post-mating Semen from the Female Reproductive Tract and Measurement of Semen Liquefaction in Mice

Published on: November 18, 2017

Area of Science:

  • Reproductive Biology
  • Animal Science
  • Flow Cytometry

Background:

  • Sex sorting bovine sperm using flow cytometry is vital for efficient cattle breeding.
  • Seminal plasma composition and storage conditions can influence sperm viability and sorting accuracy.

Purpose of the Study:

  • To investigate how seminal plasma content affects sex sorting efficacy in bovine sperm.
  • To evaluate the impact of storage duration and seminal plasma presence on sperm quality post-sorting.

Main Methods:

  • Bovine sperm were processed with varying concentrations of homologous and heterologous seminal plasma, or bovine serum albumin (BSA).
  • Sperm were stained with Hoechst 33342 and analyzed via flow cytometry for live-orientation, X sort rate, and membrane integrity.
  • Effects of 8-hour storage with or without seminal plasma on sperm motility and membrane integrity were assessed.

Main Results:

  • Lower seminal plasma concentrations (0%) during sorting increased live-oriented sperm percentages and X sort rates.
  • Variability in seminal plasma from different bulls impacted sperm membrane integrity.
  • Storage without seminal plasma improved post-thaw motility but increased membrane-impaired sperm during sorting.

Conclusions:

  • Optimizing seminal plasma levels during flow cytometry sex sorting is critical for improving sperm sorting efficiency.
  • Seminal plasma removal during sorting and storage without seminal plasma can enhance sperm quality for artificial insemination.