T2 l9The testis and spermatogenesis Flashcards

1
Q

what is the space outside the testis

A

Tunica vaginalis

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2
Q

what are the 2 main products from the testis

A

Spermatozoa

Hormones

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3
Q

where does spermatogenesis occur

A

Seminiferous tubules which are vascularised stroma containing Leydig cells

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4
Q

what is the process of spermatogenesis

A

(-some testosterone passes through to the seminiferous tubules

-converted to dihydrotestosterone by 5a-reductase in Sertoli cells )

Testosterone synthesised from acetate and cholesterol by Leydig cells

4 – 10 mg testosterone secreted daily

Principally into blood vessels but also lymph

  • Androgens are required for spermatogenesis

-

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5
Q

anatomy look at slide 3

A

how was it

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6
Q

what is the pituitary control of androgen and spermatozoa production & Proof

A

Proof: Removal of pituitary (hypophysectomy) causes testes to shrink and spermatogenesis to arrest

At puberty, androgens rise and spermatogenesis commences

LH stimulates Leydig cells to produce androgens (which are required for spermatogenesis)

FSH stimulates Sertoli cells and is required for spermatogenesis

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7
Q

describe the seminiferous tubules

A
  • surrounded by myoid cells
  • then a layer of basement membrane
  • Sertoli cells and spermatogenic cells within the tubules
  • Physiological barrier formed by gap and tight junctioned complexes between Sertoli cells
  • Creates a basal compartment containing spermatogonia
  • whilst spermatocytes,spermatids and spermatazoa are in a separate adluminal compartment
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8
Q

what are the 3 processes that spermatogenesis occurs in

A
  • Mitotic proliferation to produce lots of cells
  • Meiotic division to generate genetic diversity
  • Cell modelling to package chromosomes for delivery to the oocyte
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9
Q

describe the first phase of spermatogenesis

A
  • Germ cells of immature testis (prospermatogonia) are reactivated at puberty to undergo rounds of mitosis in the basal compartment of the tubule
  • From this self regenerating population emerge groups of cells called A1 spermatogonia which undergo a series of divisions to form a clone of cells
  • Finally after the last round of division, the clone divide to form resting primary spermatocytes.
  • Within this mitotic phase of division, although nuclear division is completed, cytoplasmic division is not, so all of the primary spermatocytes resulting from the division of a spermatogonium are linked by cytoplasmic bridges
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10
Q

describe the second stage of spermatogenesis

A

Meiosis:

Resting primary spermatocytes push through sertoli cell junctions into adluminal compartment

Enter meiotic prophase

Paired homologous chromosomes form contacts at pachytene, break, swap segments and rejoin

Very sensitive to damage at this time

First division ends with separation of homologous chromosomes to opposites ends of the meiotic spindle, cytoplasm divides forming short-lived secondary spermatocytes

These quickly divide to form haploid spermatids

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11
Q

Describe the third stage of spermatogenesis (look at pic for relevant number coord on slide 21)

A

3-Packaging

Cytoplasmic remodelling of spermatid

5: Tail for forward propulsion
4: Midpiece with mitochondria for energy
3: Nucleus with packaged chromosomes
2: Cap region forms for sperm-oocyte fusion

1: Acrosome forms to penetrate oocyte
A small residual body is the dustbin for unwanted cytoplasm, later eaten by sertoli cell

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12
Q

describe the spermatogenic cycle

A

We considered generation of sperm from a single spermatogonium

Once this process has started, new stem cells at the same location don’t start generation of clones again for a few days

The interval is constant at around 16 days, the process by which the stem cell population controls, or is controlled is unknown

The time for completion of spermatogenesis is 64 days, so there are four successive sets of clonal development (at four separate stages of the process) in one place at one time – and that’s what we see when we look down the microscope

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13
Q

describe the spermatogenic wave

A

If the seminiferous tubules are dissected longitudinally, adjacent synchronised clones of spermatogenesis are seen

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14
Q

What occurs after spermatogenesis

A

Spermatozoa wash into the rete

Through the vasa efferentia

Into the epididymis where fluid is absorbed and sperm concentrated

In the rete they can twitch: by the cauda epididymis they can swim

The process is dependent on androgen stimulation

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15
Q

What does spermatozoa mix with to form the components of semen

A

Spermatozoa mixed with secretions from seminiferous tubules, epididymis etc.

Addition of secretions from prostate, seminal vesicles and bulbourethral glands at time of ejaculation

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16
Q

what are the cellular components of the rete testis

A

Spermatozoa

Epithelial cells from tract

Spermatogenic cells

Leucocytes – risk of HIV etc

17
Q

what is the function of the fluid components of semen and what is it made of

A

Can’t be essential for fertilisation

Provide a fluid vehicle for spermatozoa

  • Nutrition (fructose, sorbitol)
  • Buffer (to protect against vaginal acidity)
  • Antioxidants (ascorbic acid, hypotaurine)
18
Q

Describe the function of the endocervix in the female & what is it stimulated and inhibited by

A

Secretes mucus with cyclical variation

Macromolecular network of mucin fibrils ?guiding spermatozoa

Sperm can penetrate from day 9, peak at time of ovulation

  • Oestrogen stimulates watery mucus
  • Progesterone inhibits secretory activity
19
Q

what does the endocervix offer the sperm

A
  • Receptive to sperm at time of ovulation, interference at other times
  • Protection from hostile vagina, and from being phagocytosed
  • Supplementation of energy requirements
  • Sperm selection by differential motility and morphology
  • Short term reservoir within endocervical crypts
  • Initiation of the next stage in sperm maturation: ‘capacitiation’
20
Q

describe the process and function of capacitation

A

Sperm recovered at ejaculation don’t fertilise ova in vitro immediately

Those from the uterus will
Have undergone capacitiation

Stripping of glycoprotein from sperm surface which accumulates in the epididymis

Causes hyperactive motility – ‘whiplash’

And make sperm responsive to signals from oocyte where we end our journey

21
Q

what 3 properties do you test in cervical mucus

A
  • Consistency (watery or viscous)
  • Spinnbarkeit (means elasticity, stickiness)
  • Ferning (crystalisation on a glass surface)
22
Q

How do you obtain sperm and what is the normal volume

A

Specimen is obtained by masturbation, collected in a clean container – (condoms often contain spermicide)

Normal ejaculated volume is 1.5 – 6 ml
Volume may be low in retrograde ejaculation, high volume may reflect abstinence or accessory gland inflammation
1.5 ml is the cut off (WHO 2010)

23
Q

what are the factors analysed in semen

look at slide 51

A

concentration and vitality :

-Sperm concentration, or density, defined as the number of sperm per ml in the total ejaculate

Normal is over 15 million per ml

-Vitality: 58% or more live spermatozoa

3- Motility: Defined as percentage of progressively motile sperm in the ejaculate
Progressively motile means they go somewhere, rather than swim around in circles

WHO uses 32% as the cut off for the lower limit of normal for progressive motility

4- Morphology -visual assessment-Greater than 4% normal forms acceptable (WHO 2010

24
Q

what is the nomenclature for describing Sperm

A

Normozoospermia
-Normal values

Oligozoospermia
-Low concentration

Asthenozoospermia-Too little motility

Teratozoospermia-Too many abnormals

Oligoasthenoterato-
zoospermia
-Mixture of the three

Azoospermia-No spermatozoa

Aspermia-No ejaculate

25
Q

look at slide 54-55

A

how did it go