EXPRESSION OF TISSUE-TYPE PLASMINOGENACTIVATOR IN SMOOTH MUSCLE CELLS OF INJUREDILIAC ARTERIES IN RABBITS
中国医学科学杂志(英文版)1996年第2期
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EXPRESSION OF TISSUE-TYPE PLASMINOGENACTIVATOR IN SMOOTH MUSCLE CELLS OF INJUREDILIAC ARTERIES IN RABBITS
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中图分类号:R364
纸质出版日期:1996
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[1]马晓莉,黄文英,佘铭鹏,李晓惠,笪冀平.EXPRESSION OF TISSUE-TYPE PLASMINOGENACTIVATOR IN SMOOTH MUSCLE CELLS OF INJUREDILIAC ARTERIES IN RABBITS[J].Chinese Medical Sciences Journal,1996(02):84-88.
EXPRESSION OF TISSUE-TYPE PLASMINOGEN ACTIVATOR IN SMOOTH MUSCLE CELLS OF INJURED ILIAC ARTERIES IN RABBITS[J]. Chinese medical sciences journal, 1996, (2).
[1]马晓莉,黄文英,佘铭鹏,李晓惠,笪冀平.EXPRESSION OF TISSUE-TYPE PLASMINOGENACTIVATOR IN SMOOTH MUSCLE CELLS OF INJUREDILIAC ARTERIES IN RABBITS[J].Chinese Medical Sciences Journal,1996(02):84-88.DOI:
EXPRESSION OF TISSUE-TYPE PLASMINOGEN ACTIVATOR IN SMOOTH MUSCLE CELLS OF INJURED ILIAC ARTERIES IN RABBITS[J]. Chinese medical sciences journal, 1996, (2).DOI:
EXPRESSION OF TISSUE-TYPE PLASMINOGENACTIVATOR IN SMOOTH MUSCLE CELLS OF INJUREDILIAC ARTERIES IN RABBITS
expression of tissue-type plasminogen activator (t-PA) in smooth muscle cells (SMCs) was measured at different intervals after the arterial injury. In the normal iliac arteries
only low levels of t-PA activity were estimated. t-PA activity in extracts of the iliac arteries increased significantlyat the 4th day after the injury
equivalent to the process that SMCs migrated from the media to the intima
and the t-PA activity was then decreased approximately to the normal level at the 7th day. Coexistent to the above data
results from in situ hybridization showed that the expression of t-PA mRNA in the intima as well as media increased also significantly at the 4th day after the arterial injury
and at the 7th day
tPA mRNA was detected only in those SMCs locating closely adjacent to the internal elastic lamina. These results suggest that t-PA might play an important role in SMC migration following endothelial injury
andantagonism of t-PA expression and/or activity within the vessel wall might be helpful in intervening the de velopment of restenosis following angioplasty.