Neocytolysis: Physiological down-regulator of red-cell mass

Clarence P. Alfrey, Lawrence Rice, Mark M. Udden, Theda B. Driscoll

Research output: Contribution to journalComment/debate

106 Scopus citations

Abstract

It is usually considered that red-cell mass is controlled by erythropoietin-driven bone marrow red-cell production, and no physiological mechanisms can shorten survival of circulating red cells. In adapting to acute plethora in microgravity, astronauts' red-cell mass falls too rapidly to be explained by diminished red-cell production. Ferrokinetics show no early decline in erythropoiesis, but red cells radiolabelled 12 days before launch survive normally. Selective destruction of the youngest circulating red cells - a process we call neocytolysis - is the only plausible explanation. A fall in erythropoietin below a threshold is likely to initiate neocytolysis, probably by influencing surface-adhesion molecules. Recognition of neocytolysis will require re-examination of the pathophysiology and treatment of several blood disorders, including the anaemia of renal disease.

Original languageEnglish (US)
Pages (from-to)1389-1390
Number of pages2
JournalLancet
Volume349
Issue number9062
DOIs
StatePublished - May 10 1997

ASJC Scopus subject areas

  • Medicine(all)

Fingerprint Dive into the research topics of 'Neocytolysis: Physiological down-regulator of red-cell mass'. Together they form a unique fingerprint.

Cite this