PubMed Health⌕ Search

PubMed · 5776553

Estimation of red cell folate activity.

Abstract

The conditions described by Hoffbrand, Newcombe, and Mollin (1966) for the estimation of red cell folate activity have been confirmed using a different method (Spray, 1964) of micro-biological assay with Lactobacillus casei. In 81 control subjects the levels of folate activity in the red cells were between 80 and 470 mmug/ml (mean 192), and in plasma between 2.1 and 13 mmug/ml (mean 4.9). In 16 patients with megaloblastic anaemia due to folic acid deficiency, the red cell folate level was between 3 and 74 mmug/ml (mean 32). In 15 of these patients the plasma level was between 0.1 and 1.0 mmug/ml; in the other patient it was 3.3 mmug/ml. Subnormal red cell levels were found in only eight out of 29 other patients whose plasma folate level was below 2.0 mmug/ml. In 26 patients with untreated pernicious anaemia, the red cell folate activity was between 44 and 280 mmug/ml (mean 129) and the plasma level was between 1.6 and 19 mmug/ml (mean 7.5).

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

G H Spray. 1969. Estimation of red cell folate activity.. https://doi.org/10.1136/jcp.22.2.212

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

E2f4 regulates fetal erythropoiesis through the promotion of cellular proliferation.

The E2F proteins are major regulators of the transcriptional program required to coordinate cell cycle progression and exit. In particular, E2f4 has been proposed to be the principal family member responsible for the regulation of cell cycle exit chiefly through its transcriptional repressive properties. We have previously shown that E2f4(-/-) mice display a marked macrocytic anemia implicating E2f4 in the regulation of erythropoiesis. However, these studies could not distinguish whether E2f4 was required for differentiation, survival, or proliferation control. Here, we describe a novel function for E2f4 in the promotion of erythroid proliferation. We show that loss of E2f4 results in an impaired expansion of the fetal erythroid compartment in vivo that is associated with impaired cell cycle progression and decreased erythroid proliferation. Consistent with these observations, cDNA microarray analysis reveals cell cycle control genes as one of the major class of genes down-regulated in E2f4(-/-) FLs, and we provide evidence that E2f4 may directly regulate the transcriptional expression of a number of these genes. We conclude that the macrocytic anemia of E2f4(-/-) mice results primarily from impaired cellular proliferation and that the major role of E2f4 in fetal erythropoiesis is to promote cell cycle progression and cellular proliferation.

Anemia, Macrocytic↗