Genetic Collagen Disorders - PowerPoint PPT Presentation

1 / 10
About This Presentation
Title:

Genetic Collagen Disorders

Description:

Genetic Collagen Disorders Osteogenesis Imperfecta Ehlers Danlos Syndrome There are others. Types of collagen Type I (most common): In bone, scar tissue, tendons ... – PowerPoint PPT presentation

Number of Views:218
Avg rating:3.0/5.0
Slides: 11
Provided by: udelEdubi
Category:

less

Transcript and Presenter's Notes

Title: Genetic Collagen Disorders


1
Genetic Collagen Disorders Osteogenesis
Imperfecta Ehlers Danlos Syndrome There are
others.
2
Types of collagen
  • Type I (most common) In bone, scar tissue,
    tendons, ligaments.
  • Type II Hyaline cartilage.
  • Type III Found in the extracellular matrix of
    earl granulation (wound healing) tissue replaced
    by type I coll. In mature scar tissue.
  • Type IV Lens of eye basal lamina beneath
    epithelium (esp. in skin, beneath epidermis)
    capillaries, including glomeruli.
  • Type V Interstitial tissue (loose conective
    tissue) placenta.
  • List goes up to XXVIII28

3
Collagen Structure Right handed helix of 3
subunits. Each subunit is a LH helix (not an
a-helix which is RH). Handednes of a helix
fingers show sense of rotation when travelling in
direction that thumb points.
Julian Voss-Andreae "Unraveling Collagen a
metaphor for aging and growth
http//en.wikipedia.org/wiki/ImageCollagentripleh
elix.png
4
Osteogenesis Imperfecta
  • General definition Genetic bone disorder in
    which bones are weak and fragile.
  • Various subtypes have been defined more
    specifically.
  • Symptoms
  • Type I (most common, mildest) Bone fragility,
    blue sclerae. Multiple fractures with minimal
    cause.
  • Type II Severe deformity and bone weakness
    death near time of birth due to respiratory
    insufficiency.
  • Type III Progressive skeletal deformity of limbs
    through childhood, and of spine in late
    childhood/early adolescence. Sclerae often
    normal.

5
Osteogenesis Imperfecta, type III

Craig W. Wiesenhutter www.cdaarthritis.com/images_
slides
6
Osteogenesis Imperfecta
  • Cause
  • Mutation to collagen gene, usually to alpha
    subunit of type I collagen gene. Usually
    autosomal dominant, inherited occasionally de
    novo.
  • Type I Collagen is relatively normal (by some
    biochemcial tests) but present in reduced
    amounts. Due to mutations that affect
    post-transcriptional- and/or post-translational
    processing more than the folding of the final
    product.
  • Type II Low amount and low quality of
    collagen.
  • Type III Collagen is present in normal amounts,
    but of insufficient quality. Often due to
    mutation in gene for alpha subunit of type I
    collagen which prevents normal triple helix from
    forming.

7
Osteogenesis Imperfecta
OI type II , type III mutation in collagen gene
? normal collagen triple helix doesnt form
8
Ehlers Danlos Syndrome
General definition Joint hypermobility with skin
changes Various subtypes have been defined more
specifically. Symptoms Unstable, flexible joints
(hypermobility) with a tendency to dislocate and
subluxate, due to ligaments which are overly
stretchable. Elastic, fragile, soft skin that
easily forms welts and scars. Intense pain where
the joints dislocate is very common. Cause Mutati
on to collagen gene, usually to type I or type V
collagen gene. Autosomal dominant.
9
Ehlers Danlos Syndrome
20-year-old man presented for consideration of
repair of a rectal prolapse that had been present
since birth. Physical examination revealed
hyperelasticity of the skin (Panel A) with easy
bruisability, hypermobility of the joints (Panel
B), and a rectal prolapse of about 15 cm in
length, which was easily reducible. Results of
laboratory tests and chromosome studies were
normal. Results of a skin biopsy showed
disorganization of collagen bundles in the
dermis. Chen and Jao (2007), NEJM 357 (11) e12.
10
Proteoglycans make extracellular matrix of
cartilage a gel Typical proteoglycan in hyaline
cartilage is a long hyaluronan (hyaluronic acid,
hyaluronate) molecule with attached aggrecan
molecules. Aggrecan is itself a proteoglycan,
i.e. a protein linked to complex carbohydrates.
Chondroitin sulfate, keratan sulfate, heparain,
and hyaluronan are glycosaminoglycans.
Hyaluronan also found in synovial fluid and
vitreous humor. Rooster comb a source for
hyaluronan which is key ingredient in Synvisc.
Aggrecan core protein
Hyaluronan backbone with aggrecans attached.
Linker protein at base of each aggrecan not
shown. (Cell shown here is not to scale aggrecan
molecules are 50-300 nm long.)
Craig W. Wiesenhutter www.cdaarthritis.com/images_
slides
Write a Comment
User Comments (0)
About PowerShow.com