The blood–testis barrier is a physical barrier between the blood vessels and the seminiferous tubules of the animal testes. The name "blood-testis barrier" is misleading as it is not a blood-organ barrier in a strict sense, but is formed between Sertoli cells of the seminiferous tubule and isolates the further developed stages of germ cells from the blood. A more correct term is the Sertoli cell barrier (SCB).
The walls of seminiferous tubules are lined with primitive germ layer cells and by Sertoli cells. The barrier is formed by tight junctions, adherens junctions and gap junctions between the Sertoli cells, which are sustentacular cells (supporting cells) of the seminiferous tubules, and divides the seminiferous tubule into a basal compartment (outer side of the tubule, in contact with blood and lymph) and an endoluminal compartment (inner side of the tubule, isolated from blood and lymph). The tight junctions are formed by intercellular adhesion molecules in between cells that are anchored to actin fibers within the cells. For the visualization of the actin fibers within the seminiferous tubules see Sharma et al.'s immunofluorescence studies.
The presence of the SCB allows Sertoli cells to control the adluminal environment in which germ cells (spermatocytes, spermatids and sperm) develop by influencing the chemical composition of the luminal fluid.
The barrier also prevents passage of cytotoxic agents (bodies or substances that are toxic to cells) into the seminiferous tubules.
The fluid in the lumen of seminiferous tubules is quite different from plasma; it contains very little protein and glucose but is rich in androgens, estrogens, potassium, inositol and glutamic and aspartic acid. This composition is maintained by blood–testis barrier.
The barrier also protects the germ cells from blood-borne noxious agents,
prevents antigenic products of germ cell maturation from entering the circulation and generating an autoimmune response, and may help establish an osmotic gradient that facilitates movement of fluid into the tubular lumen.
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Spermatogenesis is the process by which haploid spermatozoa develop from germ cells in the seminiferous tubules of the testis. This process starts with the mitotic division of the stem cells located close to the basement membrane of the tubules. These cells are called spermatogonial stem cells. The mitotic division of these produces two types of cells. Type A cells replenish the stem cells, and type B cells differentiate into primary spermatocytes.
A spermatozoon (spərˌmætəˈzoʊ.ən,_ˌspɜrmətə-; also spelled spermatozoön; : spermatozoa; ) is a motile sperm cell, or moving form of the haploid cell that is the male gamete. A spermatozoon joins an ovum to form a zygote. (A zygote is a single cell, with a complete set of chromosomes, that normally develops into an embryo.) Sperm cells contribute approximately half of the nuclear genetic information to the diploid offspring (excluding, in most cases, mitochondrial DNA).
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