Literature DB >> 27175366

Increased Expression of Lamin A/C Correlate with Regions of High Wall Stress in Abdominal Aortic Aneurysms.

Amir Malkawi1, Grisha Pirianov1, Evelyn Torsney1, Ian Chetter2, Natzi Sakalihasan3, Ian M Loftus1, Ian Nordon4, Christopher Huggins1, Nicoletta Charolidi1, Matt Thompson1, Xie Yun Xu5, Gillian W Cockerill1.   

Abstract

BACKGROUND: Since aortic diameter is the most -significant risk factor for rupture, we sought to identify stress-dependent changes in gene expression to illuminate novel molecular processes in aneurysm rupture.
MATERIALS AND METHODS: We constructed finite element maps of abdominal computerized tomography scans (CTs) of seven abdominal aortic aneurysm (AAA) patients to map wall stress. Paired biopsies from high- and low-stress areas were collected at surgery using vascular landmarks as coordinates. Differential gene expression was evaluated by Illumina Array analysis, using the whole genome DNA-mediated, annealing, selection, extension, and ligation (DASL) gene chip (n = 3 paired samples).
RESULTS: The sole significant candidate from this analysis, Lamin A/C, was validated at the protein level, using western blotting. Lamin A/C expression in the inferior mesenteric vein (IMV) of AAA patients was compared to a control group and in aortic smooth muscle cells in culture in response to physiological pulsatile stretch. -Areas of high wall stress (n = 7) correlate to those -regions which have the thinnest walls [778 µm (585-1120 µm)] in comparison to areas of lowest wall stress [1620 µm (962-2919 µm)]. Induced expression of Lamin A/C -correlated with areas of high wall stress from AAAs but was not significantly induced in the IMV from AAA patients compared to controls (n = 16). Stress-induced expression of Lamin A/C was mimicked by exposing aortic smooth muscle cells to prolonged pulsatile stretch.
CONCLUSION: Lamin A/C protein is specifically increased in areas of high wall stress in AAA from patients, but is not increased on other vascular beds of aneurysm patients, suggesting that its elevation may be a compensatory response to the pathobiology leading to aneurysms.

Entities:  

Keywords:  Aging; Nuclear lamina; Smooth muscle cells; Stretch

Year:  2015        PMID: 27175366      PMCID: PMC4851850          DOI: 10.12945/j.aorta.2015.14.069

Source DB:  PubMed          Journal:  Aorta (Stamford)        ISSN: 2325-4637


  58 in total

Review 1.  Lamins and disease: insights into nuclear infrastructure.

Authors:  K L Wilson; M S Zastrow; K K Lee
Journal:  Cell       Date:  2001-03-09       Impact factor: 41.582

2.  Lamin a truncation in Hutchinson-Gilford progeria.

Authors:  Annachiara De Sandre-Giovannoli; Rafaëlle Bernard; Pierre Cau; Claire Navarro; Jeanne Amiel; Irène Boccaccio; Stanislas Lyonnet; Colin L Stewart; Arnold Munnich; Martine Le Merrer; Nicolas Lévy
Journal:  Science       Date:  2003-04-17       Impact factor: 47.728

3.  LMNA, encoding lamin A/C, is mutated in partial lipodystrophy.

Authors:  S Shackleton; D J Lloyd; S N Jackson; R Evans; M F Niermeijer; B M Singh; H Schmidt; G Brabant; S Kumar; P N Durrington; S Gregory; S O'Rahilly; R C Trembath
Journal:  Nat Genet       Date:  2000-02       Impact factor: 38.330

4.  Simultaneous analysis of 1176 gene products in normal human aorta and abdominal aortic aneurysms using a membrane-based complementary DNA expression array.

Authors:  W S Tung; J K Lee; R W Thompson
Journal:  J Vasc Surg       Date:  2001-07       Impact factor: 4.268

5.  Accelerated ageing in mice deficient in Zmpste24 protease is linked to p53 signalling activation.

Authors:  Ignacio Varela; Juan Cadiñanos; Alberto M Pendás; Ana Gutiérrez-Fernández; Alicia R Folgueras; Luis M Sánchez; Zhongjun Zhou; Francisco J Rodríguez; Colin L Stewart; José A Vega; Karl Tryggvason; José M P Freije; Carlos López-Otín
Journal:  Nature       Date:  2005-08-03       Impact factor: 49.962

6.  High levels of 18F-FDG uptake in aortic aneurysm wall are associated with high wall stress.

Authors:  X Y Xu; A Borghi; A Nchimi; J Leung; P Gomez; Z Cheng; J O Defraigne; N Sakalihasan
Journal:  Eur J Vasc Endovasc Surg       Date:  2009-11-18       Impact factor: 7.069

Review 7.  Inflammation and cellular immune responses in abdominal aortic aneurysms.

Authors:  Koichi Shimizu; Richard N Mitchell; Peter Libby
Journal:  Arterioscler Thromb Vasc Biol       Date:  2006-02-23       Impact factor: 8.311

8.  Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome.

Authors:  Robert D Goldman; Dale K Shumaker; Michael R Erdos; Maria Eriksson; Anne E Goldman; Leslie B Gordon; Yosef Gruenbaum; Satya Khuon; Melissa Mendez; Renée Varga; Francis S Collins
Journal:  Proc Natl Acad Sci U S A       Date:  2004-06-07       Impact factor: 11.205

9.  Experimental models of abdominal aortic aneurysms.

Authors:  Janice C Tsui
Journal:  Open Cardiovasc Med J       Date:  2010-11-26

10.  Isoprenylation is required for the processing of the lamin A precursor.

Authors:  L A Beck; T J Hosick; M Sinensky
Journal:  J Cell Biol       Date:  1990-05       Impact factor: 10.539

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.