Disposition of homocysteine in rat hepatocytes and in nontransformed and malignant mouse embryo fibroblasts following exposure to inhibitors of S-adenosylhomocysteine catabolism

• Published in: Cancer research (Chicago, Ill.) Ill.), 1986-10, Vol.46 (10), p.5095-5100
• Main Authors: SVARDAL, A. M, DJURHUUS, R, REFSUM, H, UELAND, P. M
• Format: Article
• Language: English
• Subjects: Adenine - analogs & derivatives; Adenine - pharmacology; Adenosine - analogs & derivatives; Adenosine - pharmacology; Adenosine Triphosphate - analysis; Adenosylhomocysteinase; Animals; Biological and medical sciences; Cell Line; Cell Transformation, Neoplastic - metabolism; Fibroblasts - metabolism; General aspects (metabolism, cell proliferation, established cell line...); Homocysteine - analogs & derivatives; Homocysteine - metabolism; Hydrolases - antagonists & inhibitors; In Vitro Techniques; Liver - metabolism; Medical sciences; Methionine - metabolism; Rats; S-Adenosylhomocysteine - metabolism; Tumor cell; Tumors
• ISSN: 0008-5472; 1538-7445

S-Adenosylhomocysteine (AdoHcy) is catabolized to adenosine and homocysteine through the action of AdoHcy hydrolase, and this reaction is the only known source of L-homocysteine in vertebrates. The disposition of endogenously formed L-homocysteine was investigated in isolated rat hepatocytes and nontransformed and malignant C3H/10T1/2 mouse embryo fibroblasts exposed to 3-deazaaristeromycin or D-eritadenine, compounds which are potent inhibitors of AdoHcy hydrolase. Cells in suspension release large amounts of L-homocysteine into the extracellular medium whereas small amounts are retained within the intracellular compartment. The L-homocysteine egress is inhibited by 3-deazaaristeromycin or D-eritadenine in a manner which closely parallels the inhibitory effect on AdoHcy catabolism, suggesting that L-homocysteine egress may be coupled to its formation from AdoHcy. In liver cells, the accumulation of AdoHcy exceeded the inhibition of L-homocysteine egress, whereas in the fibroblasts inhibition of egress equalled the accumulation of AdoHcy. Inhibition of AdoHcy catabolism was associated with an increase in both free and protein bound L-homocysteine in liver cells, whereas depletion of intracellular L-homocysteine occurred in the mouse embryo fibroblasts under these conditions. These data suggest that some properties of nucleoside analogues may be related to their effects on L-homocysteine metabolism. Furthermore, L-homocysteine is exported into the extracellular medium in proportion to the formation from AdoHcy, and extracellular L-homocysteine may be a measure of the balance between L-homocysteine formation and utilization.