Inhibitory Smads suppress pancreatic stellate cell activation through negative feedback in chronic pancreatitis

Hao Lin; Beibei Dong; Liang Qi; Yingxiang Wei; Yusha Zhang; Xiaotian Cai; Qi Zhang; Jia Li; Ling Li

doi:10.21037/atm-20-4282

Inhibitory Smads suppress pancreatic stellate cell activation through negative feedback in chronic pancreatitis

Ann Transl Med. 2021 Mar;9(5):384. doi: 10.21037/atm-20-4282.

Authors

Hao Lin^{1

2}, Beibei Dong³, Liang Qi³, Yingxiang Wei⁴, Yusha Zhang⁵, Xiaotian Cai⁵, Qi Zhang⁵, Jia Li⁴, Ling Li^{2

3}

Affiliations

¹ Department of Clinical Science and Research, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, China.
² Institute of Pancreas, Southeast University, Nanjing, China.
³ Department of Endocrinology, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, China.
⁴ Department of Ultrasound, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, China.
⁵ School of Medicine, Southeast University, Nanjing, China.

Abstract

Background: Activation of pancreatic stellate cells (PSCs) is a key cause of chronic pancreatitis (CP), while inhibition of transforming growth factor-β (TGF-β) signaling renders PSCs inactive. Inhibitory Smads (I-Smads) impede TGF-β intracellular signaling and may provide a way to alleviate CP. Thus, we aimed to investigate the molecular mechanism of I-Smads in CP animals and freshly-isolated PSCs.

Methods: Sixteen male C57BL/6 mice were randomly divided into two groups; a control group (treated with saline) and a CP group (treated with caerulein) for 6 weeks. Masson's staining was performed to identify fibrosis, and immunohistochemistry (IHC) was performed to measure the levels of Smad6 between the two groups. An improved method derived from internal digestion was used to isolate PSCs from male Sprague Dawley rats. Quantitative real-time polymerase chain reaction (qRT-PCR) and immunofluorescence staining were used to measure the messenger ribonucleic acid (mRNA) and protein levels of alpha-smooth muscle actin (α-SMA). Plasmids of I-Smads or SB431542 were transfected into freshly-isolated PSCs, and relative mRNA levels of marker genes were quantified by qRT-PCR. The two-tailed Student's t-test was performed to assess significance.

Results: The Smad6 protein level was significantly higher in the pancreas tissue of CP mice compared to the control group. A large number of PSCs were isolated from rat pancreas using an improved isolating method and were confirmed by quiescent and active PSC markers including cluster differentiation antigen 133 (CD133), perilipin 2 (Plin2), α-SMA, Desmin, and collagen 1 (Col1). The mRNA levels of both Smad6 and Smad7 were down-regulated during freshly-isolated PSC activation. Over-expression of both Smad6 and Smad7 in freshly-isolated PSC reduced the mRNA level of α-SMA, glial fibrillary acidic protein (GFAP), Desmin, Col1, Col3, and fibronectin 1 (Fn1) significantly. SB431542 reduced the mRNA level of α-SMA, Col1, Col3, and Fn1 significantly in freshly-isolated PSCs.

Conclusions: This study demonstrated that CP promoted the expression of I-Smads, which suppressed the activation of freshly-isolated PSCs via a negative feedback loop.

Keywords: I-Smads; chronic pancreatitis; freshly isolated pancreatic stellate cells; negative feedback.