کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1904681 1534651 2015 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Bone marrow-derived c-jun N-terminal kinase-1 (JNK1) mediates liver regeneration
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی سالمندی
پیش نمایش صفحه اول مقاله
Bone marrow-derived c-jun N-terminal kinase-1 (JNK1) mediates liver regeneration
چکیده انگلیسی


• Cell proliferation is linked to JNK1-deficiency after partial resection.
• Reduced liver proliferation is associated to lower activation of IL-6/STAT-3 axis.
• The hematopoietic-derived JNK1 is relevant in mediating the hepatic regeneration.
• A synergistic function of JNK1 in hepatocytes and hematopoietic cells was found.

Liver regeneration is controlled by a complex network of signaling molecules, and a prominent role for c-jun N-terminal kinase has been suggested during this process. In the present study, we aimed to characterize and define the cell-type-specific contribution of JNK1 activation during liver regeneration. We used hepatocyte-specific JNK1 knockout mice (JNK1Δhepa) using the cre/lox-P system. We performed partial hepatectomy (PH) in WT, JNK1Δhepa and JNK1−/− animals and investigated time-points up to 72 h after PH. Additionally, bone marrow transplantation experiments were conducted in order to identify the contribution of hematopoietic cell-derived JNK1 activation for liver regeneration. Our results show that liver regeneration was significantly impaired in JNK1−/− compared to JNK1Δhepa and WT animals. These data were evidenced by lower BrdU incorporation and decreased cell cycle markers such as Cyclin A, Cyclin D, E2F1 and PCNA 48 h after PH in JNK1−/− compared with JNK1Δhepa and WT livers. In JNK1−/− mice, our findings were associated with a reduced acute phase response as evidenced by a lower activation of the IL-6/STAT3/SAA-1 cascade. Additionally, CD11b+Ly6G+-cells were decreased in JNK1−/− compared with JNK1Δhepa and WT animals after PH. The transplantation of bone marrow-derived JNK1−/− into WT recipients caused significant reduction in liver regeneration. Interestingly, the transplantation of JNK1−/− into mice lacking JNK1 in hepatocytes only partially delayed liver regeneration. In summary, we provide evidence that (1) JNK1 in hematopoietic cells is crucial for liver regeneration, and (2) a synergistic function between JNK1 in hepatocytes and hematopoietic-derived cells is involved in the hepatic regenerative response.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease - Volume 1852, Issue 1, January 2015, Pages 137–145
نویسندگان
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