Differential expression of apolipoprotein E messenger RNA within the rat liver lobule determined by in situ hybridization

Mara Massimi, Steven R. Lear, David L. Williams, Albert L. Jones, Sandra K. Erickson – 30 December 2003 – Apolipoprotein (Apo) E plays a key role in the metabolism of lipoproteins. It also modulates immunoregulation, cell growth and differentiation and the response to nerve injury. The liver is a major site of ApoE synthesis. Most of the circulating ApoE is thought to be of hepatic origin with most synthesized in hepatocytes.

Expression of hepatitis C virus NS5B protein: Characterization of its RNA polymerase activity and RNA binding

Koji Ishii, Yoshinobu Tanaka, Chan‐Choo Yap, Hideki Aizaki, Yoshiharu Matsuura, Tatsuo Miyamura – 30 December 2003 – The nonstructural protein 5B (NS5B) of hepatitis C virus (HCV) is considered to possess RNA‐dependent RNA polymerase (RdRp) activity and to play an essential role for the viral replication. In this study, we expressed the NS5B protein of 65 kd by a recombinant baculovirus. With the highly purified NS5B protein, we established anin vitrosystem for RdRp activity by using poly(A) as a template and a 15‐mer oligo(U) (oligo(U)15) as a primer.

Comparison of immune reactivity and pharmacokinetics of two hepatitis B immune globulins in patients after liver transplantation

Ruth Adler, Rifaat Safadi, Yoseph Caraco, Mina Rowe, Amos Etzioni, Yaffa Ashur, Daniel Shouval – 30 December 2003 – Hepatitis B virus (HBV) immune globulin (HBIg) administration will prevent HBV graft reinfection in HBV patients after orthotopic liver transplantation (OLT). However, the expenditure for such prophylaxis is extremely high ranging between $2,000 to $10,000 per month in various countries for an undefined period and presumably for life. As a consequence, there is a need for introduction of additional and less expensive modes of treatment.

Gap junctional communication and regulation of the glycogenic response to insulin by cell density and glucocorticoids in cultured fetal rat hepatocytes

Mashiat U. Siddiqui, Samia Benatmane, Jean‐Luc Zachayus, Christiane Plas – 30 December 2003 – Cell culture studies have revealed that metabolic functions of the adult hepatocyte are related to cell density. Development of the glycogenic response to insulin under glucocorticoid control was investigated in 15‐ and 18‐day‐old fetal rat hepatocytes plated at different cell densities.

Secretory low–molecular‐weight phospholipases A2 and their specific receptor in bile ducts of patients with intrahepatic calculi: Factors of chronic proliferative cholangitis

Junichi Shoda, Masahito Kano, Toru Asano, Tatsuro Irimura, Tetsuya Ueda, Ryu Iwasaki, Masato Furukawa, Junichi Kamiya, Yuji Nimura, Takeshi Todoroki, Yasushi Matsuzaki, Naomi Tanaka – 30 December 2003 – Intrahepatic calculi is characterized by an intractable course and frequent recurrences, requiring multiple operative interventions. Chronic proliferative cholangitis, an active and long‐standing inflammation of the stone‐containing bile ducts with the hyperplasia of epithelia and the proliferation of the duct‐associated mucus glands, may underlie the complex nature of the disease.

Functions of the fibrinolytic system in human ito cells and its control by basic fibroblast and platelet‐derived growth factor

Gabriella Fibbi, Marco Pucci, Cecilia Grappone, Giulia Pellegrini, Renata Salzano, Alessandro Casini, Stefano Milani, Mario Del Rosso – 30 December 2003 – During liver fibrogenesis, hepatic stellate cells (HSC) proliferate and migrate under the influence of growth factors, including platelet‐derived growth factor (PDGF) and basic‐fibroblast growth factor (b‐FGF). The plasminogen activation system regulates extracellular matrix (ECM) catabolism and cell movement.

Hepatitis B virus X protein transactivates the inducible nitric oxide synthase promoter

Maria José Amaro, Javier Bartolomé, Vicente Carreño – 30 December 2003 – The capability of hepatitis B virus (HBV) to increase the transcription of the human hepatic inducible nitric oxide synthase (iNOS) by transactivating its promoter has been studied. We have observed by reverse‐transcription polymerase chain reaction (RT‐PCR) that although the mRNA for the iNOS was almost undetectable in the human hepatoblastoma cell line, HepG2, it was constitutively expressed in the 2.2.15 cell line (a derivative of the HepG2 that produces complete HBV particles).

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