Then We made the sperm into a clot of congealed blood; then of that clot We made a (foetus) lump; then we made out of that lump bones and clothed the bones with flesh; then we developed out of it another creature. So blessed be Allah, the best to create!

SAHIH INTERNATIONAL:Then We made the #spermdrop into a clinging clot, and We made the clot into a lump [of flesh], and We made [from] the lump, bones, and We covered the bones with flesh; then We developed him into another creation. So blessed is Allah, the best of creators.
By Evangelist Isa Omofo Johnbest aka #Kumfarijikunfayakun http://www.uwyo.edu/wjm/repro/spermat.htm. @#Chrislam@#Quran3:45-57-@#YeareGods-John10:24* https://quran.com/23/14?translations=101,22,18,84,21,20,19,17,95
Spermatogenesis is the process of sperm cell development. Rounded immature sperm cells undergo successive mitotic and meiotic divisions (spermatocytogenesis) and a metamorphic change (spermiogenesis) to produce spermatozoa.
Mitosis and meiosis. Mitosis is the process of cell duplication – two daughter cells are formed with exactly the same DNA and chromosomal content of the original diploid (2N) mother cell. Human cells contain 46 chromosomes – 22 pairs of homologous autosomes and one pair of sex chromosomes.
Mitosis (M) encompasses just one step in the eukaryotic cell cycle: G1 > S > G2 > M > C.( PICKTHALL
Then fashioned We the drop a clot, then fashioned We the clot a little lump, then fashioned We the little lump bones, then clothed the bones with flesh, and then produced it as another creation. So blessed be Allah, the Best of creators! ) Cells grow during the dominant G1 phase. Replication of chromosomes occurs in the S phase. Preparation for mitosis takes place during G2 – replication of organelles and synthesis of microtubules. Interphase includes the combined stages G1, S, and G2. During mitosis: chromosomes condense, the nuclear envelope disappears, and spindle fibers begin to form from microtubules (prophase); centromeres of duplicate sister chromatids align along the spindle equator (metaphase); chromatids separate and migrate toward opposite poles (anaphase); the mitotic apparatus is disassembled, autonomous nuclear envelopes are established, and the chromosomes uncoil (telophase). The final stage of the cell cycle, when cell division actually occurs, is called
Then We made the #Nutfah into a clot (a piece of thick coagulated blood), then We made the clot into a little lump of flesh, then We made out of that little lump of flesh bones, then We clothed the bones with flesh, and then We brought it forth as another creation. So blessed be Allah, the Best of creators.

(23:14) then We made this drop into a clot, then We made the clot into a lump, then We made the lump into bones, then We clothed the bones with flesh,2 and then We caused it to grow into another creation.3 Thus Most Blessed is Allah, the Best of all those that create.4

Thereafter We created the sperm-drop into a clot, (Or: embryo) then We created the clot into a chewed up morsel, then We created the chewed up morsel into bones, then We dressed the bones (in) flesh; thereafter We brought him into being as another creation. So Supremely Blessed be Allah, The Fairest of creators.


Then We made the seed a clot, then We made the clot a lump of flesh, then We made (in) the lump of flesh bones, then We clothed the bones with flesh, then We caused it to grow into another creation, so blessed be Allah, the best of the creators.


Then We turned the sperm-drop into a clot, then We turned the clot into a fetus-lump, then We turned the fetus-lump into bones, then We clothed the bones with flesh; thereafter We developed it into another creature. So, glorious is Allah, the Best of the creators.


then We developed the drop into a clinging clot ˹of blood˺, then developed the clot into a lump ˹of flesh˺, then developed the lump into bones, then clothed the bones with flesh, then We brought it into being as a new creation. So Blessed is Allah, the Best of Creators.

  • #Meiosis is a special process of reductional cell division; it results in the formation of four gametes containing half (1N) the number of chromosomes found in somatic cells. Haploid gametes unite at fertilization to create a diploid zygote. Remember that in mammals the heterogametic male (XY) determines the sex of the embryo. Approximately one-half of spermatozoa contain either an X or Y chromosome (the sex chromosomal complement of mammalian females is XX, and therefore, ova can only contribute an X chromosome to the offspring). Genes carried on the X chromosome that inhibit spermatogenesis are inactivated in XY somatic cells.
    Steps of meiosis are outlined in Table 3-3. Meiosis differs from mitosis in two critical respects. During prophase of meiosis I, chromosomes pair along their length and come in contact in discrete areas of synapsis (chiasmata). Chromatids can exchange base pairs by crossing-over. The recombination of segments of chromosomes allows for continual generation of genetic variability (ie., rapid evolutionary progress) and provides a mechanism for correcting damage in the DNA helix. Secondly, nonidentical sister chromatids do not replicate between serial nuclear divisions. Meiosis II is essentially mitotic.
    (An unusual natural circumstance exists in the creeping vole – males normally have OY gametes; the X chromosome is eliminated from the cell line by nondisjunction and the companion XXY cell presumably does not complete meiosis [in most mammals OY is lethal]).
    Spermatocytogenesis. During spermatocytogenesis primitive cells called spermatogonia proliferate by mitosis. Several different types of spermatogonia have been identified (A-0 through A-4, intermediate [IN], and B). Only the discriminating anatomist can actually distinguish among types of spermatogonia. Mitosis ends when a B spermatogonium yields two primary spermatocytes.
    The diploid number of primary spermatocytes is halved during meiosis. A primary spermatocyte is transformed into two secondary spermatocytes during meiosis I – these cells then in turn are converted into (1N) spermatids during meiosis II. The second meiotic division is rapid (and therefore very few secondary spermatocytes can be identified in histological sections). Spermatocytes and spermatids tend to be larger than their ancestral spermatogonia.
    Males have an almost unlimited capacity to produce germ cells; this is accomplished by replenishment of A spermatogonia early in mitosis. Although the mechanics of renewal are not totally understood, it appears that a stem cell (A-0) divides into an A-1 spermatogonia and an operative copy of itself. The A-1 cell becomes dedicated to spermatocytogenesis and the A-0 cell is kept in reserve for future divisions.
    Endogenous damage to the the genetic material (eg., base deamination, depurination, methylation, oxidative insult) is inevitable in proliferative cells – a battery of repair mechanisms assure that the DNA fidelity of gametes is sustained.
    Spermiogenesis. Throughout spermatocytogenesis cells retain a rounded configuration (Figure 3-23). Spermatids undergo a dramatic change in form during spermiogenesis – into the streamline spermatozoa adapted for fertilization. Spermiogenesis involves nuclear condensation, formation of the acrosomal cap, and development of a tail. The acrosome is derived from the Golgi apparatus. Centrioles (points of organization of spindle fibers) migrate to a postnuclear region after the completion of meiosis. The distal centriole provides a template for accretion of cytoskeletal elements comprising the contractile lattice of the tail. Mitochondria become concentrated into the sheath of the middle piece. Cells do not divide during spermiogenesis (Figure 3-24).
    Spermatogenic cycle and wave. If one closely examines serial cross-sections of a seminiferous tubule you will discover that sperm cells differentiate in distinctive associations. Each spermatogenic association has been classified as a stage of the seminiferous epithelial cycle. A spermatogenic cycle is defined as the time it takes for the reappearance of the same stage within a given segment of the tubule. Each stage of the cycle follows in an orderly sequence along the length of the tubule. The distance between the same stage is called the spermatogenic wave. One tubule can contain numerous complete waves. Adjacent segments of the tubule evidently communicate in some unknown manner.
    The number of stages within a spermatogenic cycle and the number of cycles required for the completion of spermatogenesis varies between species. There are 12 different stages of the cycle in the bull of about 14 days each; approximately four cycles within a given region of the tubule occur before an A1 spermatogonia is transformed into a spermatozoa. Six stages have been noted in man; four 16-day cycles are needed to complete spermatogenesis. The linear pattern of the spermatogenic cycle is less ordered in man than in farm animals or rodents.
    Hormonal regulation. Spermatogonia continue to divide, but in reduced numbers, after hypophysectomy. Spermatocytogenesis is completely arrested at the primary spermatocyte stage in hypophysectomized animals; this step is restored by testosterone. Androgen-binding protein (the testicular counterpart of SHBG) sequesters testosterone within the seminiferous tubule (and caput epididymis). Meiosis II is hormonally-independent. Follicle-stimulating hormone participates in spermiogenesis. Estradiol and DHT are also involved in the spermatogenic process.
    Hormonal effects on sperm cells are not direct, but are mediated through Sertoli cells. Biochemical and biophysical facets of sperm-Sertoli interactions in spermatogenesis are largely unknown. Rate of production of spermatozoa is not influenced by endocrine therapy.
    Blood-testis barrier. As sperm cells mature they move between Sertoli cells from the basal toward the adluminal compartment of the seminiferous tubule. Because nucleotide recombinations can occur during meiosis I, the genetic code of chromosomes of gametes can differ from that of somatic parent cells (ie., progeny cells might express cell-surface antigens that are recognized by the host as foreign and thus be eliminated by humoral or cellular immune mechanisms). Occluding junctions that interconnect adjacent Sertoli cells shield secondary spermatocytes, spermatids, and spermatozoa from autoimmune recognition (Figure 3-25). The blood-testis barrier also acts to conserve certain products of Sertoli cells within the seminiferous tubule, such as ABP. The epithelial syncytium of this barrier extends through the epididymis.
    (Vasectomy can lead to a breakdown in the blood-testis barrier in laboratory animals and subhuman primates; as a result, an autoimmune response is mounted against sperm antigens released into the periphery. Immune complexes can lodge within the kidneys and adhere to walls of blood vessels causing renal damage and atherosclerosis; possible complications of this nature, although not detected thusfar, need to be monitored closely in long-term vasectomized men.)
    Effect of temperature. Sperm cells will not mature at core body temperature in most mammals (spermatogenic DNA polymerase b and recombinase activities exhibit unique temperature optima); to adapt, the testes assume an external position. Testicular descent from the abdomen normally transpires during fetal or neonatal life.
    If the testes fail to descend into the scrotum, a condition called cryptorchidism, the male will be sterile; gone uncorrected (by surgery or androgen treatment) spermatogonia will eventually degenerate. The stallion and boar are the most prone to cryptorchidism among the domesticated species (because the condition has a genetic predisposition, it is not advisable to use unilateral/restored animals for breeding purposes). Cryptorchidism does not have a major effect on testicular output of testosterone.
    Testicular descent is permanent in many mammals (eg., domesticated animals and primates). Sometimes high ambient temperatures are associated with infertility. A transient condition of “summer sterility” is common in rams. In other species (eg., rodents) the inguinal canals remain patent, and the testes periodically descend or retract; this activity is coordinated in the wild with the mating season. The testes of hibernating mammals often descend when body temperature begins to rise after awakening. A few mammals do not have scrotal sacs (eg., monotremes, armadillos, sloths, elephants, rhinoceroses, seals, dolphins, and whales) and the testes remain within the abdomen.; these animals have a low body temperature. Notwithstanding, the internal testes of birds produce viable gametes in spite of very high abdominal body temperatures. From an evolutionary perspective it is difficult to reconcile the hazardous location of pendulous testes.
    Scrotal temperature is a few degrees lower than internal body temperature. Several compensatory mechanisms aid in maintaining testicular temperature within defined limits. For efficient dissipation of heat, the scrotum lacks subcutaneous fat and is rich in sweat glands. A two-muscle system lowers and lifts the testis. The tunica dartos is a muscular layer of the scrotum. The cremaster muscle extends from the body wall through the inguinal canal, surrounding the spermatic cord. When environmental temperature is elevated, the muscles relax, and the testes are lowered from the body. Under conditions of cold, the muscles contract, pulling the testes toward the warmth generated by the body. Scrotal surface area contributing to loss of heat is decreased when skin of the scrotum becomes wrinkled due to contraction of the tunica dartos. Finally, a convoluted network of testicular arteries and veins, the pampiniform plexus, is responsible for counter-current exchange of heat. Warm arterial systemic blood entering the testis is cooled by returning venous blood, and visa-versa (testosterone is also transferred from venous to arterial blood, concentrating androgen within the testis). Arteries and veins are coiled around each other – providing a large surface area of contact (Figure 3-26).
    Spermiation. Spermiation is the process by which spermatozoa are released from the seminiferous epithelium into the lumen of the tubule. Most of the “excess baggage” (cytoplasm and organelles) of the spermatid is discarded within the seminiferous epithelium in the form of a residual body (Figures 3-23 and 3-27). A small amount of cytoplasmic material, the cytoplasmic droplet, remains attached within the neck region or around the middle piece (Figure 3-10) as the spermatozoon makes its way into the epididymis.
    Further maturations. Seminiferous spermatozoa lack motility and fertilizing capacity. During transit through the epididymis, which takes approximately two weeks, the cytoplasmic droplet migrates distally along the tail of the spermatozoon (Figure 3-28) and falls off; this event is correlated with an increase in cellular motility (normal motility and morphology of an ejaculate should be > 60-70%). Nevertheless, in some species the full fertilizing potential of spermatozoa is not gained until cells are affected by secretions of the female reproductive tract; these spermatozoa are said to be “capacitated.”