Sperm (: sperm or sperms) is the male reproductive cell, or gamete, in anisogamous forms of sexual reproduction (forms in which there is a larger, female reproductive cell and a smaller, male one). Sperm cells contribute approximately half of the nuclear gene to the diploid offspring (excluding, in most cases, mitochondrial DNA). Animals produce motile sperm with a tail known as a flagellum, which are known as spermatozoa, while some red algae and fungi produce non-motile sperm cells, known as spermatia. contain non-motile sperm inside pollen, while some more basal plants like ferns and some have motile sperm.
Sperm cells form during the process known as spermatogenesis, which in ( and ) takes place in the seminiferous tubules of the . This process involves the production of several successive sperm cell precursors, starting with spermatogonia, which differentiate into . The spermatocytes then undergo meiosis, reducing their Ploidy by half, which produces . The spermatids then mature and, in animals, construct a tail, or flagellum, which gives rise to the mature, motile sperm cell. This whole process occurs constantly and takes around 3 months from start to finish.
Sperm cells cannot divide and have a limited lifespan, but after fusion with during fertilization, a new organism begins developing, starting as a totipotent zygote. The human sperm cell is haploid, so that its 23 can join the 23 chromosomes of the female egg to form a diploid cell with 46 paired chromosomes. In mammals, sperm is stored in the epididymis and released through the penis in semen during ejaculation.
The word sperm is derived from the Greek word , sperma, meaning "seed".
A widespread hypothesis states that sperm evolved rapidly, but there is no direct evidence that sperm evolved at a fast rate or before other male characteristics.
The nuclear DNA in sperm cells is Ploidy, that is, they contribute only one copy of each paternal chromosome pair. Mitochondrion in human sperm contain no or very little DNA because mtDNA is degraded while sperm cells are maturing, hence they typically do not contribute any genetic material to their offspring.
In mammals, sperm cells normally come in two types, "female" and "male", named for the resulting sex of the fertilized zygote each produces after fusing with the ovum. Sperm cells that produce female (karyotype XX) offspring carry an X-chromosome, while sperm cells that produce male ( XY) offspring carry a Y-chromosome. Errors of meiosis may lead to the formation of sperm containing different arrangements of sex chromosomes, either altogether missing ( monosomy, designated " 0"), or in multiples ( trisomy), such as " XX", " XY", etc... some of the conditions known as Disorders of Sex Development (DSD) are the result of fertilization by such defective sperm.
The sperm cell of Homo sapiens is the small Gamete produced by males, and can only survive in warm environments; upon leaving the body, it starts to degrade, thereby decreasing the total sperm quality.
Semen has an alkaline nature and the spermatozoa do not reach full motility (hypermotility) until they reach the vagina, where the alkaline pH is neutralized by acidic vaginal fluids. This gradual process takes 20–30 minutes. During this period, fibrinogen from the forms a clot, securing and protecting the sperm. Just as they become hypermotile, fibrinolysin from the prostate gland dissolves the clot, allowing the sperm to progress optimally.
Exposure of males to certain lifestyle, environmental or occupational hazards may increase the risk of Aneuploidy spermatozoa. In particular, risk of aneuploidy is increased by tobacco smoking, and occupational exposure to benzene, insecticides, and perfluorinated compounds. Increased aneuploidy of spermatozoa often occurs in association with increased DNA damage. DNA fragmentation and increased in situ DNA susceptibility to denaturation, the features similar to these seen during apoptosis of somatic cells, characterize abnormal spermatozoa in cases of male infertility.
Although DNA repair has long been considered impossible in human spermatozoa due to the high level of DNA compaction in these cells, human spermatozoa possess a truncated base excision repair pathway that is mediated by 8-oxoguanine DNA glycosylase 1 (OGG1). Thus mature spermatozoa appear to have a limited capacity to mount a DNA repair response to oxidative stress.
The blood-testis barrier, maintained by the tight junctions between the of the seminiferous tubules, prevents communication between the forming spermatozoa in the testis and the blood vessels (and immune cells circulating within them) within the interstitial space. This prevents them from eliciting an immune response. The blood-testis barrier is also important in preventing toxic substances from disrupting spermatogenesis.
Sperm have an olfactory Chemotaxis, and after reaching the , must undergo a period of capacitation before penetration of the ovum.
During fertilization, the sperm provides three essential parts to the oocyte: (1) a signalling or oocyte-activating factor (OAF), which causes the metabolically dormant oocyte to activate; (2) the haploid paternal genome; (3) the centriole, which is responsible for forming the centrosome and microtubule system.
The spermatozoon is characterized by a minimum of cytoplasm and the most densely packed DNA known in . Compared to mitosis chromosomes in , sperm DNA is at least sixfold more highly condensed.
Human sperm genetics has been associated with human evolution, per a 2020 study.
In humans, recombination rates differ between maternal and paternal DNA:
The initial change is called "hyperactivation", which causes a change in spermatozoa motility. They swim faster and their tail movements become more forceful and erratic.
A recent discovery links hyperactivation to a sudden influx of calcium ion into the tails. The whip-like tail (flagellum) of the sperm is studded with formed by proteins called CatSper. These channels are selective, allowing only calcium ions to pass. The opening of CatSper channels is responsible for the influx of calcium. The sudden rise in calcium levels causes the flagellum to form deeper bends, propelling the sperm more forcefully through the viscous environment. Sperm hyperactivity is necessary for breaking through two physical barriers that protect the egg from fertilization.
The second process in sperm activation is the acrosome reaction. This involves releasing the contents of the acrosome, which disperse, and the exposure of enzymes attached to the inner acrosomal membrane of the sperm. This occurs after the sperm first meets the egg. This lock-and-key type mechanism is species-specific and prevents the sperm and egg of different species from fusing. There is some evidence that this binding is what triggers the acrosome to release the enzymes that allow the sperm to fuse with the egg.
ZP3, one of the proteins that make up the zona pellucida, then binds to a partner molecule on the sperm. Enzymes on the inner acrosomal membrane digest the zona pellucida. After the sperm penetrates the zona pellucida, part of the sperm's cell membrane then fertilization with the egg cell's membrane, and the contents of the head diffuse into the egg.
Upon penetration, the oocyte is said to have become Ovum activation. It undergoes its secondary meiotic division, and the two haploid nuclei (paternal and maternal) fuse to form a zygote. In order to prevent polyspermy and minimise the possibility of producing a Triploidy zygote, several changes to the egg's zona pellucida renders them impenetrable shortly after the first sperm enters the egg.
In 2016, scientists at Nanjing Medical University claimed they had produced cells resembling mouse spermatids from mouse embryonic stem cells artificially. They injected these spermatids into mouse eggs and produced pups.
Spermatozoa are produced in the seminiferous tubules of the in a process called spermatogenesis. Round cells called spermatogonia divide and differentiate eventually to become spermatozoa. During copulation, the cloaca or vagina gets insemination, and then the spermatozoa move through chemotaxis to the ovum inside an oviduct.
DNA damages present in sperm cells in the period after meiosis but before fertilization may be repaired in the fertilized egg, but if not repaired, can have serious deleterious effects on fertility and the developing embryo. Human sperm cells are particularly vulnerable to free radical attack and the generation of oxidative DNA damage, such as that from 8-Oxo-2'-deoxyguanosine.
The postmeiotic phase of mouse spermatogenesis is very sensitive to environmental genotoxic agents, because as male germ cells form mature sperm they progressively lose the ability to repair DNA damage. Irradiation of male mice during late spermatogenesis can induce damage that persists for at least seven days in the fertilizing sperm cells, and disruption of maternal DNA double-strand break repair pathways increases sperm cell-derived chromosomal aberrations. Treatment of male mice with melphalan, a bifunctional alkylating agent frequently employed in chemotherapy, induces DNA lesions during meiosis that may persist in an unrepaired state as germ cells progress through DNA repair-competent phases of spermatogenic development. Such unrepaired DNA damages in sperm cells, after fertilization, can lead to offspring with various abnormalities.
For example, if more than 1.0 million progressive motile sperm per milliliter are found, it will be recommended to have sexual intercourse, and if that fails, the next step will be intrauterine insemination and later conventional in vitro fertilization.
In addition to ejaculation, it is possible to extract sperm through testicular sperm extraction.
On the global market, Denmark has a well-developed system of human sperm export. This success mainly comes from the reputation of Danish sperm donors for being of high quality and, in contrast with the law in the other Nordic countries, gives donors the choice of being either anonymous or non-anonymous to the receiving couple. Assisted Reproduction in the Nordic Countries ncbio.org Furthermore, Nordic sperm donors tend to be tall and highly educated FDA Rules Block Import of Prized Danish Sperm Posted Aug 13, 08 7:37 AM CDT in World, Science & Health and have altruistic motives for their donations, partly due to the relatively low monetary compensation in Nordic countries. More than 50 countries worldwide are importers of Danish sperm, including Paraguay, Canada, Kenya, and Hong Kong. However, the Food and Drug Administration (FDA) of the US has banned import of any sperm, motivated by a risk of transmission of Creutzfeldt–Jakob disease, although such a risk is insignificant, since artificial insemination is very different from the route of transmission of Creutzfeldt–Jakob disease. The prevalence of Creutzfeldt–Jakob disease for donors is at most one in a million, and if the donor was a carrier, the infectious proteins would still have to cross the blood-testis barrier to make transmission possible.
Semen cryopreservation can be used for far longer storage durations. For human spermatozoa, the longest reported successful storage with this method is 21 years.
Some species of Drosophilidae produce the largest known spermatozoon found in nature. Drosophila melanogaster produces sperm that can be up to 1.8 mm, while its relative Drosophila bifurca produces the largest known spermatozoon, measuring over 58 mm in length. In Drosophila melanogaster, the entire sperm, tail included, gets incorporated into the oocyte cytoplasm, however, for Drosophila bifurca only a small portion of the tail enters the oocyte.
The wood mouse Apodemus sylvaticus possesses spermatozoa with falciform morphology. Another characteristics which makes these gametocytes unique is the presence of an apical hook on the sperm head. This hook is used to attach to the hooks or to the flagella of other spermatozoa. Aggregation is caused by these attachments and mobile trains result. These trains provide improved motility in the female reproductive tract and are a means by which fertilization is promoted.
The postmeiotic phase of mouse spermatogenesis is very sensitive to environmental Genotoxicity agents, because as male germ cells form mature spermatozoa they progressively lose the ability to repair DNA damage. Irradiation of male mice during late spermatogenesis can induce damage that persists for at least 7 days in the fertilizing spermatozoa, and disruption of maternal DNA double-strand break repair pathways increases spermatozoa-derived chromosomal aberrations. Treatment of male mice with melphalan, a bifunctional alkylation frequently employed in chemotherapy, induces DNA lesions during meiosis that may persist in an unrepaired state as germ cells progress through DNA repair-competent phases of spermatogenic development. Such unrepaired DNA damages in spermatozoa, after fertilization, can lead to offspring with various abnormalities.
such as Arbacia punctulata are ideal organisms to use in sperm research, they spawn large numbers of sperm into the sea, making them well-suited as for experiments.
The spermatozoa of are usually longer than those of .
The of , and some produce motile sperm cells, contrary to pollen grains employed in most gymnosperms and all . This renders sexual reproduction in the absence of water impossible, since water is a necessary medium for sperm and egg to meet. Algae and lower plant sperm cells are often multi-flagellated (see image) and thus morphologically different from animal spermatozoa.
Some algae and fungi produce non-motile sperm cells, called spermatia. In higher plants and some algae and fungi, fertilization involves the migration of the sperm nucleus through a fertilization tube (e.g. pollen tube in higher plants) to reach the egg cell.
Motile sperm are also produced by many and the gametophytes of , and some such as and ginkgo. The sperm cells are the only flagellated cells in the life cycle of these plants. In many ferns and , cycads and ginkgo they are multi-flagellated (carrying more than one flagellum).
In , the sperm cells are amoeboid and crawl, rather than swim, towards the egg cell.
Because spermatia cannot swim, they depend on their environment to carry them to the egg cell. Some , such as Polysiphonia, produce non-motile spermatia that are spread by water currents after their release. The spermatia of rust fungi are covered with a sticky substance. They are produced in flask-shaped structures containing nectar, which attract Fly that transfer the spermatia to nearby hyphae for fertilization in a mechanism similar to insect pollination in .
Fungal spermatia (also called pycniospores, especially in the Uredinales) may be confused with conidia. Conidia are that germinate independently of fertilization, whereas spermatia are that are required for fertilization. In some fungi, such as Neurospora crassa, spermatia are identical to microconidia as they can perform both functions of fertilization as well as giving rise to new organisms without fertilization.
In some , fertilization also involves sperm nuclei, rather than cells, migrating toward the egg cell through a fertilization tube. form sperm nuclei in a syncytium antheridium surrounding the egg cells. The sperm nuclei reach the eggs through fertilization tubes, similar to the pollen tube mechanism in plants.
In 1841 the Swiss anatomist Albert von Kölliker wrote about spermatozoon in his work Untersuchungen über die Bedeutung der Samenfäden (Studies on the importance of spermatozoa).
Avoidance of immune system response
Anatomy
Sperm size
Sperm activation
Origin
Assisted reproductive technology
Sperm quality
MMP and capacitation
Market for human sperm
Forensic analysis
Artificial storage
Sperm in other animals
Sperm in plants and other organisms
Motile sperm cells
Non-motile sperm cells
Sperm nuclei
Sperm centrioles
Sperm tail formation
History
See also
Citations
General and cited sources
External links
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