In vivo inactivation of erythrocyte S-adenosylhomocysteine hydrolase by 2'-deoxyadenosine in adenosine deaminase-deficient patients.

MS Hershfield, NM Kredich, DR Ownby… - The Journal of …, 1979 - Am Soc Clin Investig
MS Hershfield, NM Kredich, DR Ownby, H Ownby, R Buckley
The Journal of clinical investigation, 1979Am Soc Clin Investig
The cytotoxic nucleoside 2'-deoxyadenosine is excreted in excessive amounts by
individuals with genetic deficiency of adenosine deaminase, and may be in part responsible
for the severe combined immune dysfunction from which they suffer. Earlier studies from this
laboratory showed that 2'-deoxyadenosine causes the irreversible inactivation of the
enzyme S-adenosylhomocysteine hydrolase by an active site-directed," suicide-like"
process. In this communication we have demonstrated similar inactivation of S …
The cytotoxic nucleoside 2'-deoxyadenosine is excreted in excessive amounts by individuals with genetic deficiency of adenosine deaminase, and may be in part responsible for the severe combined immune dysfunction from which they suffer. Earlier studies from this laboratory showed that 2'-deoxyadenosine causes the irreversible inactivation of the enzyme S-adenosylhomocysteine hydrolase by an active site-directed, "suicide-like" process. In this communication we have demonstrated similar inactivation of S-adenosylhomocysteine hydrolase in hemolysate and in intact erythrocytes, as well as a striking deficiency of S-adenosylhomocysteine hydrolase activity in the erythrocytes of three adenosine deaminase-deficient patients. In vivo suicide-like inactivation of S-adenosylhomocysteine hydrolase by 2'-deoxyadenosine may contribute to the cytotoxicity of 2'-deoxyadenosine and to the immune dysfunction in adenosine deaminase deficiency.
The Journal of Clinical Investigation