Identification of argininosuccinate lyase as a hypoxia-responsive gene in rat hepatocytes

Background/Aims: The differential oxygenation of periportal and perivenous hepatocytes has been demonstrated as a major determinant in the zonated exp ression of certain metabolic pathways in the liver. We have searched for no vel genes whose expression could be modulated by hypoxia in cultured rat he patocytes. Methods: Primary cultures of rat hepatocytes were incubated under normoxic (21% oxygen) or hypoxic (3% oxygen) conditions for 6 h, Differences in gene expression under both conditions were analyzed using the technique of diff erential display by means of PCR. Results: We have identified the enzyme argininosuccinate lyase (ASL) as bei ng downregulated by hypoxia. ASL is a cytosolic protein which participates in urea metabolism. ASL expression was time-dependently reduced in hypoxia. Hypoxia modulated the responses of this gene to the two main hormonal sign als which induce ASL mRNA: glucocorticoids and cAMP. ASL mRNA levels decrea sed in response to ATP-reducing agents. CoCl2 mimicked the effect of hypoxi a, suggesting the implication of a hemoprotein in this response. Hypoxia di d not affect ASL mRNA stability, indicating that this effect occurs at the transcriptional level. Conclusions: Our observations suggest that differences in oxygen levels acr oss the hepatic parenchyma could participate in the zonated expression of A SL.