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Confocal Microscopic Evidence of Decreased α–actin Expression within Rabbit Cerebral Artery Smooth Muscle Cells after Subarachnoid Haemorrhage

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Abstract

Our objective was to determine whether subarachnoid haemorrhage modifies cerebral artery smooth muscle cell phenotype and the contractile protein α-actin measured 7 days after haemorrhage. We used a rabbit subarachnoid haemorrhage model and immunofluorescence labelling of α-smooth muscle actin, vimentin and desmin. The paired comparison between the haemorrhage and sham rabbits was performed using confocal laser-scanning microscopy. We found in the haemorrhage group significantly less intense α-actin immunostaining (p = 0.036) and more intense vimentin immunostaining (p = 0.043) but no significant change in the intensity of desmin staining. Our results indicate an absolute decrease after subarachnoid haemorrhage in the amount of functional α-actin and in the light of the literature may suggest a certain degree of dedifferentiation of smooth muscle cells in the cerebral artery wall.

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References

  • Bevan JA, Bevan RD, Frazee JP (1987) Functional arterial changes in chronic cerebrovasospasm in monkeys: an in vitro assessment of the contribution to arterial narrowing. Stroke 18: 472-481.

    Google Scholar 

  • Clower BR, Smith RR, Haining JL, Lockard J (1981) Constrictive endarteropathy following experimental subarachnoid hemorrhage. Stroke 12: 501-508.

    Google Scholar 

  • Debus E, Weber K, Osborn M (1983) Monoclonal antibodies to desmine, the muscle-specific intermediate filament protein. EMBO J 2: 2305-2312.

    Google Scholar 

  • Evans RM (1998) Vimentin: the conundrum of the intermediate filament gene family. Bioessays 20: 79-86.

    Google Scholar 

  • Fatigati V, Murphy RA (1984) Actin and tropomyosin variants in smooth muscles. Dependence on tissue type. J Biol Chem 10(259): 14383-14388.

    Google Scholar 

  • Findlay JM, Weir BK, Kanamaru K, Espinosa F (1989) Arterial wall changes in cerebral vasospasm. Neurosurgery 25: 736-745.

    Google Scholar 

  • Gabbiani G, Rungger-Brandle E, de Chastonay C, Franke WW (1982) Vimentin-containing smooth muscle cells in aortic intimal thickening after endothelial injury. Lab Invest 47: 265-269.

    Google Scholar 

  • Hughes JT, Schianchi PM (1978) Cerebral artery spasm. A histological study at necropsy of the blood vessels in cases of subarachnoid hemorrhage. J Neurosurg 48: 515-525.

    Google Scholar 

  • Hungerford JE, Little CD (1999) Developmental biology of the vascular smooth muscle cell: building a multilayered vessel wall. J Vasc Res 36: 2-27.

    Google Scholar 

  • Kacem K, Seylaz J, Aubineau P (1996) Differential processes of vascular smooth muscle cell differentiation within elastic and muscular arteries of rats and rabbits: an immunofluorescence study of desmin and vimentin distribution. Histochem J 28: 53-61.

    Google Scholar 

  • Kim P, Sundt TM Jr, Vanhoutte PM (1989) Alterations of mechanical properties in canine basilar arteries after subarachnoid hemorrhage. J Neurosurg 71: 430-436.

    Google Scholar 

  • Liszczak TM, Varsos VG, Black PM, Kistler JP, Zervas NT (1983) Cerebral arterial constriction after experimental subarachnoid hemorrhage is associated with blood components within the arterial wall. J Neurosurg 58: 18-26.

    Google Scholar 

  • MacDonald RL, Weir BK, Young JD, Grace MG (1992) Cytoskeletal and extracellular matrix proteins in cerebral arteries following subarachnoid hemorrhage in monkeys. J Neurosurg 76: 81-90.

    Google Scholar 

  • Mayberg MR, Okada T, Bark DH (1990) The significance of morphological changes in cerebral arteries after subarachnoid hemorrhage. J Neurosurg 72: 626-633.

    Google Scholar 

  • Minami N, Tani E, Maeda Y, Yamaura I, Nakano A (1993) Immunoblotting of contractile and cytoskeletal proteins of canine basilar artery in vasospasm. Neurosurgery 33: 698-705.

    Google Scholar 

  • Nelson RJ, Perry S, Hames TK, Pickard JD (1990) Transcranial Doppler ultrasound studies of cerebral autoregulation and subarachnoid hemorrhage in the rabbit. J Neurosurg 3: 601-610.

    Google Scholar 

  • Oka Y, Ohta S, Todo H, Kohno K, Kumon Y, Sakaki S (1996) Protein synthesis and immunoreactivities of contraction-related proteins in smooth muscle cells of canine basilar artery after experimental subarachnoid hemorrhage. J Cereb Blood Flow Metab 16: 1335-1344.

    Google Scholar 

  • Osborn M, Caselitz J, Weber K (1981) Heterogeneity of intermediate filament expression in vascular smooth muscle: a gradient in desmin positive cells from the rat aortic arch to the level of the arteria iliaca communis. Differentiation 20: 196-202.

    Google Scholar 

  • Owens GK (1995) Regulation of differentiation of vascular smooth muscle cells. Physiol Rev 75: 487-517.

    Google Scholar 

  • Quax W, Meera Khan P, Quax-Jeuken Y, Bloemendal H (1985) The human desmin and vimentin genes are located on different chromosomes. Gene 38: 189-196.

    Google Scholar 

  • Schwartz SM, Campbell GR, Campbell JH (1986) Replication of smooth muscle cells in vascular disease. Circ Res 58: 427-444.

    Google Scholar 

  • Shishido T, Suzuki R, Qian L, Hirakawa K (1994) The role of superoxide anions in the pathogenesis of cerebral vasospasm. Stroke 25: 864-868.

    Google Scholar 

  • Skalli O, Ropraz P, Trzeciak A, Benzonana G, Gillessen D, Gabbiani G (1986) A monoclonal antibody against α-smooth muscle actin: a new probe for smooth muscle differentiation. J Cell Biol 103: 2787-2796.

    Google Scholar 

  • Smith R, Clower B, Grotendorst G, Yabuno N, Cruse J (1985) Arterial wall changes in early human vasospasm. Neurosurgery 16: 171-176.

    Google Scholar 

  • Takemae T, Branson PJ, Alksne JF (1984) Intimal proliferation of cerebral arteries after subarachnoid blood injection in pigs. J Neurosurg 61: 494-500.

    Google Scholar 

  • Varsos V, Liszczak T, Han D, Kistler J, Vielma J, Black P, Heros R, Zervas N (1983) Delayed cerebral vasospasm is not reversible by aminophylline, nifedipine, or papaverine in a ‘two-hemorrhage’ canine model. J Neurosurg 58: 11-17.

    Google Scholar 

  • Vorkapic P, Bevan R, Bevan J (1990) Pharmacologic irreversible narrowing in chronic cerebrovasospasm in rabbits is associated with functional damage. Stroke 21: 1478-1484.

    Google Scholar 

  • Vorkapic P, Bevan R, Bevan J (1991) Longitudinal time course of reversible and irreversible components of chronic cerebrovasospasm of the rabbit basilar artery. J Neurosurg 74: 951-955.

    Google Scholar 

  • Yamashima T, Kida S, Yamamoto S (1986) An electron microscopic study of cerebral vasospasm with resultant myonecrosis in cases of subarachnoid haemorrhage, meningitis and trans-sylvian surgery. J Neurol 233: 348-357.

    Google Scholar 

  • Zuccarello M, Lewis A, Upputuri S, Farmer J, Anderson D (1994) Effect of remacemide hydrochloride on subarachnoid hemorrhage-induced vasospasm in rabbits. J Neurotrauma 11: 691-698.

    Google Scholar 

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Gomis, P., Kacem, K., Sercombe, C. et al. Confocal Microscopic Evidence of Decreased α–actin Expression within Rabbit Cerebral Artery Smooth Muscle Cells after Subarachnoid Haemorrhage. Histochem J 32, 673–678 (2000). https://doi.org/10.1023/A:1004115432660

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