Hepatocyte nuclear factor 4α negatively regulates connective tissue growth factor during liver regeneration. 2020

Junmei Zhou, and Xiaowei Sun, and Lu Yang, and Liqun Wang, and Gai Ran, and Jinhui Wang, and Qi Cao, and Lizi Wu, and Andrew Bryant, and Chen Ling, and Liya Pi
Department of Pediatrics, University of Florida, Gainesville, FL, USA.

Liver regeneration after injury requires fine-tune regulation of connective tissue growth factor (Ctgf). It also involves dynamic expression of hepatocyte nuclear factor (Hnf)4α, Yes-associated protein (Yap), and transforming growth factor (Tgf)-β. The upstream inducers of Ctgf, such as Yap, etc, are well-known. However, the negative regulator of Ctgf remains unclear. Here, we investigated the Hnf4α regulation of Ctgf post-various types of liver injury. Both wild-type animals and animals contained siRNA-mediated Hnf4α knockdown and Cre-mediated Ctgf conditional deletion were used. We observed that Ctgf induction was associated with Hnf4α decline, nuclear Yap accumulation, and Tgf-β upregulation during early stage of liver regeneration. The Ctgf promoter contained an Hnf4α binding sequence that overlapped with the cis-regulatory element for Yap and Tgf-β. Ctgf loss attenuated inflammation, hepatocyte proliferation, and collagen synthesis, whereas Hnf4α knockdown enhanced Ctgf induction and liver fibrogenesis. These findings provided a new mechanism about fine-tuned regulation of Ctgf through Hnf4α antagonism of Yap and Tgf-β activities to balance regenerative and fibrotic signals.

UI MeSH Term Description Entries
D008115 Liver Regeneration Repair or renewal of hepatic tissue. Liver Regenerations,Regeneration, Liver,Regenerations, Liver
D011485 Protein Binding The process in which substances, either endogenous or exogenous, bind to proteins, peptides, enzymes, protein precursors, or allied compounds. Specific protein-binding measures are often used as assays in diagnostic assessments. Plasma Protein Binding Capacity,Binding, Protein
D003094 Collagen A polypeptide substance comprising about one third of the total protein in mammalian organisms. It is the main constituent of SKIN; CONNECTIVE TISSUE; and the organic substance of bones (BONE AND BONES) and teeth (TOOTH). Avicon,Avitene,Collagen Felt,Collagen Fleece,Collagenfleece,Collastat,Dermodress,Microfibril Collagen Hemostat,Pangen,Zyderm,alpha-Collagen,Collagen Hemostat, Microfibril,alpha Collagen
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000091102 YAP-Signaling Proteins Signal transducing adaptor proteins that were initially identified by their association with YES PROTO-ONCOGENE PROTEIN. They are downstream components of the HIPPO-SIGNALING PATHWAY, and act as transcriptional co-activators for TEAD TRANSCRIPTION FACTORS. YAP Intracellular Signaling Proteins,Yes-Associated Proteins,YAP Signaling Proteins,Yes Associated Proteins
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D015854 Up-Regulation A positive regulatory effect on physiological processes at the molecular, cellular, or systemic level. At the molecular level, the major regulatory sites include membrane receptors, genes (GENE EXPRESSION REGULATION), mRNAs (RNA, MESSENGER), and proteins. Receptor Up-Regulation,Upregulation,Up-Regulation (Physiology),Up Regulation
D016212 Transforming Growth Factor beta A factor synthesized in a wide variety of tissues. It acts synergistically with TGF-alpha in inducing phenotypic transformation and can also act as a negative autocrine growth factor. TGF-beta has a potential role in embryonal development, cellular differentiation, hormone secretion, and immune function. TGF-beta is found mostly as homodimer forms of separate gene products TGF-beta1, TGF-beta2 or TGF-beta3. Heterodimers composed of TGF-beta1 and 2 (TGF-beta1.2) or of TGF-beta2 and 3 (TGF-beta2.3) have been isolated. The TGF-beta proteins are synthesized as precursor proteins. Bone-Derived Transforming Growth Factor,Platelet Transforming Growth Factor,TGF-beta,Milk Growth Factor,TGFbeta,Bone Derived Transforming Growth Factor,Factor, Milk Growth,Growth Factor, Milk
D048868 Adaptor Proteins, Signal Transducing A broad category of carrier proteins that play a role in SIGNAL TRANSDUCTION. They generally contain several modular domains, each of which having its own binding activity, and act by forming complexes with other intracellular-signaling molecules. Signal-transducing adaptor proteins lack enzyme activity, however their activity can be modulated by other signal-transducing enzymes Signal Transducing Adaptor Proteins
D049109 Cell Proliferation All of the processes involved in increasing CELL NUMBER including CELL DIVISION. Cell Growth in Number,Cellular Proliferation,Cell Multiplication,Cell Number Growth,Growth, Cell Number,Multiplication, Cell,Number Growth, Cell,Proliferation, Cell,Proliferation, Cellular

Related Publications

Junmei Zhou, and Xiaowei Sun, and Lu Yang, and Liqun Wang, and Gai Ran, and Jinhui Wang, and Qi Cao, and Lizi Wu, and Andrew Bryant, and Chen Ling, and Liya Pi
October 2020, Hepatology (Baltimore, Md.),
Junmei Zhou, and Xiaowei Sun, and Lu Yang, and Liqun Wang, and Gai Ran, and Jinhui Wang, and Qi Cao, and Lizi Wu, and Andrew Bryant, and Chen Ling, and Liya Pi
March 2019, Biochemistry and biophysics reports,
Junmei Zhou, and Xiaowei Sun, and Lu Yang, and Liqun Wang, and Gai Ran, and Jinhui Wang, and Qi Cao, and Lizi Wu, and Andrew Bryant, and Chen Ling, and Liya Pi
November 2014, Hepatology (Baltimore, Md.),
Junmei Zhou, and Xiaowei Sun, and Lu Yang, and Liqun Wang, and Gai Ran, and Jinhui Wang, and Qi Cao, and Lizi Wu, and Andrew Bryant, and Chen Ling, and Liya Pi
December 2015, The Journal of biological chemistry,
Junmei Zhou, and Xiaowei Sun, and Lu Yang, and Liqun Wang, and Gai Ran, and Jinhui Wang, and Qi Cao, and Lizi Wu, and Andrew Bryant, and Chen Ling, and Liya Pi
March 2011, Drug metabolism and disposition: the biological fate of chemicals,
Junmei Zhou, and Xiaowei Sun, and Lu Yang, and Liqun Wang, and Gai Ran, and Jinhui Wang, and Qi Cao, and Lizi Wu, and Andrew Bryant, and Chen Ling, and Liya Pi
October 2003, Biochemical and biophysical research communications,
Junmei Zhou, and Xiaowei Sun, and Lu Yang, and Liqun Wang, and Gai Ran, and Jinhui Wang, and Qi Cao, and Lizi Wu, and Andrew Bryant, and Chen Ling, and Liya Pi
July 1998, The Journal of pathology,
Junmei Zhou, and Xiaowei Sun, and Lu Yang, and Liqun Wang, and Gai Ran, and Jinhui Wang, and Qi Cao, and Lizi Wu, and Andrew Bryant, and Chen Ling, and Liya Pi
June 2013, Journal of digestive diseases,
Junmei Zhou, and Xiaowei Sun, and Lu Yang, and Liqun Wang, and Gai Ran, and Jinhui Wang, and Qi Cao, and Lizi Wu, and Andrew Bryant, and Chen Ling, and Liya Pi
November 2013, FEBS letters,
Junmei Zhou, and Xiaowei Sun, and Lu Yang, and Liqun Wang, and Gai Ran, and Jinhui Wang, and Qi Cao, and Lizi Wu, and Andrew Bryant, and Chen Ling, and Liya Pi
June 2020, American journal of physiology. Cell physiology,
Copied contents to your clipboard!