Epithelial stem cells in Hutchinson-Gilford progeria syndrome
Hutchinson-Gilford progeria syndrome (HGPS) and restrictive dermopathy (RD) are two rare genetic disorders that affect children. Complications from cardiovascular disease, including atherosclerosis, are the most common cause of death in HGPS, which occurs at around 13 years of age. RD patients seldom live beyond their first few weeks of life, with their characteristically tight skin causing death by restricting respiration.
These diseases are caused by mutations that cause the accumulation of prelamin A, or one of its truncated forms, prelamin AΔ50 (progerin). The majority of HGPS cases are due to a de novo single point mutation in exon 11 of the LMNA gene, c.1824C>T (p.G608G). This gene encodes the A-type lamins, which are major proteins of the inner nuclear lamina. Most cases of RD are caused by loss of function mutations in the lamin A processing zmpste24 enzyme.
Inducible and tissue specific mouse models were used to examine the mechanistic effects of progerin. The mouse models carried an artificial minigene which encoded lamin A with the the most common HGPS mutation. This minigene was targeted to the skin in Papers I and II by means of the keratin 5 (K5) promoter, and to the cardiovascular system in Paper III by means of the sm22α promoter.
In Paper I, the effects of progerin were examined with a focus on postnatal skin. Our results showed a reduced population of keratinocytes with stem cell properties. This was associated with downregulation of P63 (an epidermal stem cell maintenance protein) in the HGPS mice, an effect also found with increased ageing in HGPS patients cells.
In Paper II, to test the hypothesis that the more severe symptoms in RD, as compared with HGPS, are due to the higher levels of farnesylated lamin A produced in RD, the LMNA c. 1824C>T, p.G608G was expressed in embryonic skin causing early postnatal death, as in the human condition. This was accompanied by increased inflammation, prolonged expression of the lamin B receptor gene, and arrested skin development.
In Paper III a model was designed to examine the effects of progerin in the cardiovascular system. However the expression of the reverse sm22α transactivator was barely detectable in arteries, and this low level of expression was not sufficient to induce expression of the target human lamin A gene.
This thesis offers novel findings about the intricate molecular disease mechanisms underlying HGPS and RD.
List of scientific papers
I. Stem cell depletion in Hutchinson-Gilford progeria syndrome. Rosengardten Y, McKenna T, Grochová D, Eriksson M. Aging Cell. 2011 Dec;10(6):1011-20
https://doi.org/10.1111/j.1474-9726.2011.00743.x
II. Embryonic expression of the common progeria lamin A splice mutation arrests postnatal skin development. McKenna T, Rosengardten Y, Viceconte N, Baek J-H, Grochová D, Eriksson M. Aging Cell. 2014 Apr;13(2):292–302.
https://doi.org/10.1111/acel.12173
III. Low levels of the reverse transactivator fail to induce target transgene expression in vascular smooth muscle cells. Viceconte N, McKenna T, Eriksson M. PLoS ONE. 2014;9(8):e104098.
https://doi.org/10.1371/journal.pone.0104098
History
Defence date
2015-01-23Department
- Department of Medicine, Huddinge
Publisher/Institution
Karolinska InstitutetMain supervisor
Eriksson, MariaPublication year
2015Thesis type
- Doctoral thesis
ISBN
978-91-7549-795-2Number of supporting papers
3Language
- eng