Expression of alpha smooth muscle actin in living donor liver transplant recipients
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Masataka Hirabaru
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Kyoko Mochizuki
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Mitsuhisa Takatsuki
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Department of Surgery,Nagasaki University Graduate School of Biomedical Sciences,Nagasaki 852-8501,JapanDepartment of Surgery,Nagasaki University Graduate School of Biomedical Sciences,Nagasaki 852-8501,Japan
Mitsuhisa Takatsuki
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Akihiko Soyama
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Department of Surgery,Nagasaki University Graduate School of Biomedical Sciences,Nagasaki 852-8501,JapanDepartment of Surgery,Nagasaki University Graduate School of Biomedical Sciences,Nagasaki 852-8501,Japan
Akihiko Soyama
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Taiichiro Kosaka
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Tamotsu Kuroki
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Isao Shimokawa
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Susmu Eguchi
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[1] Department of Surgery,Nagasaki University Graduate School of Biomedical Sciences,Nagasaki 852-8501,Japan
[2] Department of Investigative Pathology,Nagasaki University Graduate School of Biomedical Sciences,Nagasaki 852-8501,Japan
Recently,there have been reports from liver biopsies that showed the progression of liver fibrosis in liver transplant patients after the cessation of immunosuppression.Herein,we focused on activated hepatic stellate cells expressing alpha smooth muscle actin(α-SMA)to understand the correlation between immunosuppressant medication and liver fibrosis.The study enrolled two pediatric patients who underwent living donor liver transplantation and ceased immunosuppressant therapy.The number ofα-SMA-positive cells in the specimens obtained by liver biopsy from these two patients showed a three-fold increase compared with the number from four transplanted pediatric patients who were continuing immunosuppressant therapy.In addition,theα-SMA-positive area evaluated using the WinRooF image processing software program continued toincrease over time in three adult transplanted patients with liver fibrosis,and theα-SMA-positive area was increasing even during the pre-fibrotic stage in these adult cases,according to a retrospective review.Therefore,α-SMA could be a useful marker for the detection of early stage fibrosis.