1979
DOI: 10.1002/ajh.2830070303
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Hemopoietic precursor cells in human peripheral blood

Abstract: Human peripheral blood contains two types of stem cells that differentiate along the granulocytic pathway. They are separable by their ability to form colonies in agar in vitro (CFU-C) and in plasma clots in diffusion chambers in vivo (CFU-DG). Kinetic studies suggest that CFU-DG represents an intermediate between the still hypothetical human pluripotent stem cell and CFU-C.

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Cited by 16 publications
(10 citation statements)
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“…(b) The human CFU-DG and CFU-C behave quite differently in an in vivo culture. The number of CFU-DG decreases progressively during a 4-d period, whereas the CFU-C decline initially then increase above the original inoculum number (20). In this work the distinctiveness of CFU-C and CFU-DG is supported by the observed differences in response to hypotonicity.…”
Section: Resultssupporting
confidence: 68%
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“…(b) The human CFU-DG and CFU-C behave quite differently in an in vivo culture. The number of CFU-DG decreases progressively during a 4-d period, whereas the CFU-C decline initially then increase above the original inoculum number (20). In this work the distinctiveness of CFU-C and CFU-DG is supported by the observed differences in response to hypotonicity.…”
Section: Resultssupporting
confidence: 68%
“…Results fromii this and an earlier study (20) suggest that both human and murine CFU-DG are more primitive than CFU-C. Still unanswered remains the question of whether CFU-DG is an expression of differentiation of the pluripotent stem cell; i.e., is it identical with murine CFU-S or its human equivalent, or is it an intermediate stem cell that is not yet comitted to granulocytic differentiation.…”
Section: Resultsmentioning
confidence: 84%
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“…However, it should be emphasized that the results obtained in the present study do not exclude the possibility of an increased total concentration of CFU-D in NLR, because of higher marrow cellularity in these patients. Similar progenitor number in NLR and controls could also result from the fact that using the DC technique we have investigated the proliferation of a more primitive granulocyte progenitor population, different from that which forms colonies in vitro [18,29]. This cell compartment might be less affected during infection or could be already influenced by feedback inhibition of granulopoiesis [21,22].…”
Section: Discussionmentioning
confidence: 92%
“…In this study we monitored the early phases of granulocytopoiesis in patients with chronic neutropenia by determining the number of cells ' which form granulocyte-containing colonies in diffusion chambers in mice (CFU-DG) and the number of cells which form granulocytic colonies in agar in vitro (CFU-C). Several studies suggest the existence of a parent-progeny relationship between CFU-DG and CFU-C precursors (8)(9)(10). 11 white males employed by a chemical plant were referred to the University of Virginia Hospital for evaluation of chronic neutropenia.…”
mentioning
confidence: 99%