The short but happy life of a sperm Flashcards

1
Q

What are the two main products of the testes?Where are they made?

A

Spermatozoa

Hormones

*Manufactured in different compartments

Spermatogenesis occurs in the seminiferous tubule- vascularised stroma containing leydig cells

Testosterone synthesised from acetate and cholesterol by leydig cells

  • mainly into blood vessels but also lymph
  • some to seminiferous tubule (DHT which testosterone is converted to be 5a-reductase in sertoli cells)
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2
Q

State the anatomical structures within the testis

draw a pic and label

A
Spermatic cord
Blood vessels
Ductus deferens
Epididymis - storage of sperm
Ductus epididymis
Seminiferous tubule
Lobule
Straight tubulr
Rete testis- network of tubules
Tunica albuginea- septa forming lobules
Tunica vaginalis- parietal and visceral layer
Efferent duct- connect to the epididymis
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3
Q

What is the function of androgens?

A

Maintain reproductive and sexual function

Required fro spermatogenesis

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4
Q

Describe pituitary control of spermatogenesis

A
  • Production of androgens and spermatozoa related functionally
  • At puberty : increase in androgens–> beginning of spermatogenesis

Hypophysectomy –> testes shrink and spermatogenesis arrests

  • LH stimulates leydig cells to produce androgens
  • FSH stimlates sertoli cells
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5
Q

Describe the seminiferoud tubule

A
  • Contains sertoli cells and spermatogenic cells
    Physiological barrier formed by gap and tight junctions between sertoli cells. This creates a basal compartment containing spermatogonia, whilst spermatocytes, spermatids and spermatozia are in seperate adluminal compartments
  • Surrounded my myoid cells and basement membranes
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6
Q

Consider spermatogenesis

Describe step 1

A

MITOSIS (to increase numbers)

Begin as spermatogonium (2n)

  • germ cells of immature testis (prospermatogonia) are reactivated at puberty to undergo rounds of mitosis in the basal compartment of the tubule
  • from this emerge cells called A1 spermatogoma whichi undergo a series of devisions to form lots of cells

End as primary spermatocytes (2n)

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7
Q

Consider spermatogenesis

Describe step 2

A

MEIOSIS (to generate genetic diversity)

Begin as primary spermatocytes (2n)

  • Resting primary spermatocytes push through sertoli cell junctions into adluminal compartment
  • enter meiotic prophase
  • paired homologous chromosomes form contacts at pachytene, break and swap segments and rejoin (damage sensitive)
  • results in seperation of homologous chromosomes to opposite ends of meiotic spindle, cytoplasm divides forming short lived secondary spermatocytes (2n)

These quickly divide to form haploid spermatoids (n)

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8
Q

Consider spermatogenesis

Describe step 3
Outline all the structures in a sperm and their functions

A

PACKAGING

  • cytoplasmic remodelling of spermatoid
    1. Acrosome - to penetrate oocyte (a small residualbody is the dustbin for unwanted cytoplasm, later eaten by sertoli cells)
    2. Cap region forms for spem-oocyte fusion
    3. Nucleus with packaged chromosome
    4. Midpiece with mitochondria for energy
    5. Tail for forward projection
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9
Q

Describe the spermatogenic cycle

A

One process of spermatogenesis occurs, new stem cells at the same location dont start generation of clones again for a few days

  • The interval is constant around 16 days: the process by which the stem cell population control, or is controlled is unknown
  • 64 days: time for completion of spermatogenesis –> 4 successive sets of clonal development (at 4 seperate stages of the process)/place/time
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10
Q

How is the spermatogenic cycle controlled?

A

Spatial and temporal organisation

  • If all spermatogonia were activated simultaneously, mature spermatozia would be produced every 16 days –> episodic fertility. If activated randomly –> continuous production

In reality, small regions seem to activated together in wedges around the tubu;e
- If seminiferoud tubules are dissected longitudinally, adjacent synchronised clones of spermatogenesis are seen (“WAVE-LIKE”)

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11
Q

Where does the final stage of maturation of spermatozoa occur?

A

Spermatozia wash into the rete, thorugh the vasa efferentia and into the epididymis where fluis is absorbed and sperm concentrated

In the rete they can twitch, by the cauda epididymis they can swim. This process is dependent on androgen stimulation

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12
Q

What are the components of semen?

A
  1. Spermatozoa mixed with epididymis secretions and seminiferous secretions
  2. Cellular components: leukocytes (risk of HIV), spermatogenic cells, spermatozoa, epithelial cells from tract
  3. Secretions from prostate, seminal vesicles and bulbourethral glands at time of ejactulation
  4. Fluid components: nutrition (fructose, sorbitol), buffer (to protect against vaginal acidity, antioxidants (ascorbic acid, hypotaurine)
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13
Q

What does the endocervix do?

A
  • Secrete musuc with cyclical variation
  • Macromolecular network of mucin fibrils (guide spermatozoa)
  • Oestrogen stimulates watery mucus
  • Progesterone inhibits secretory activity
  • Allows sperm penetration from day 9, pak at time of ovulation
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14
Q

What does the endocervix offer sperm?

A
  • Receptive to sperm at ovulation time
  • Protection from hostile vagina and from phagocytosis
  • Supplementation of energy requirement
  • Sperm selection by differential motility and morphology
  • Short term reservoir within endocervical crypts
  • Initiation of next stage in sperm maturation (CAPACITIATION)
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15
Q

What is capacitiation?

A

Stripping of glycoprotein from sperm surface which accumulates in the epididymis

  • Sperm dont fertilise in vitro immediately, in uterus it does after it undergoes capacitiation
  • This causes hyperactivity motility - ‘whiplash’ and makes sperm response to signals from oocyte
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16
Q

State the properties of cervical mucus

How could you test for these?

A
  1. Consistency can be watery or viscous
  2. Spirinbarkeit: elasticity, stickiness
  3. Ferning? (crystallisation on a glass surface)

Crude assessment of a complex physiological situation. Detailed testing can follow (eg looking at spermatozoa penetrating mucus and assessing motility)

17
Q

How do you collect a semen specimen?

What parameters are you assessing?

A

Specimen is obtained by masturbation, collected in a clean container (not condoms- contain spermacides)

Volume: 1.5-6ml (low in retrograde ejaculation, high if practising abstinence/ accessory gland inflammation)

Concentration and vitality: >15 million/ml, vitality >58%

Motility: percentage of progressively motile sperm (dont just go round in a circle)

Morphology: requires visual assessment, should by >4%
e.g. large/small head, double tail, double head, tapered head, coiled tail, shapeless head, immature form

18
Q

Define the following terms

  1. Normozoospermia
  2. Oligozoospermia
  3. Asthenozoospermia
  4. Teratozoospermia
  5. Oligoasthenoteratozoospermia
  6. Azoospermia
  7. Aspermia
A
  1. Normal concentration
  2. Low concentration
  3. Too little motility
  4. Too many abnormals
  5. Low conc, low motility highly abnormal sperm
  6. No spermatozoa
  7. No ejaculate