Journal of Ovarian Research · 2014 · 23 citations · 30 references
Life SciencesNutritionNutritional SciencesAgingReproductive PhysiologyStem Cell BiologyHematopoietic Stem Cell BiologyMammalian Life HistoryNutritional Effects On ReproductionRodent NutritionRodent ReproductionStem Cell PhysiologyCirculating Hematopoietic Stem CellsGrowth Under Nutritional RestrictionHematopoietic Stem Cell AgingInsulin-like Growth Factor-1Life Span ExtensionMouse Embryonic Stem CellsNutritional Effects On FertilityNutritional Regulation Of Development
BACKGROUND: Low calorie intake, or calorie restriction (CR) without malnutrition, has been demonstrated in several animal species, including mice, to increase both median and maximum lifespan as well as delay reproductive senescence. Our previous work demonstrated a positive correlation between life span and the number of very small embryonic-like stem cells (VSELs) in long living Laron dwarf mice. These animals have very low levels of circulating insulin-like growth factor 1 (IGF-1) in peripheral blood (PB), maintain higher numbers of hematopoietic stem cells (HSPCs) in bone marrow (BM), and display prolonged fecundity compared with wild type littermates. Since CR lowers the level of IGF-1 in PB, we become interested in the effect of CR on the number of VSELs and HSPCs in BM as well as on the morphology of ovaries and testes. METHODS: In our studies four-week-old female and male mice were subjected to CR by employing an alternate-day ad libitum feeding diet for a period of 9 months. RESULTS: We observed that mice on CR had a higher number of BM-residing VSELs than control mice fed ad libitum. These changes correlated with higher numbers of HSPCs in BM, spleen, and peripheral blood (PB) as well as with an increase in the number of primordial and primary follicles in ovaries. At the same time, however, no changes were observed in the testes of mice under CR. CONCLUSION: We conclude that CR positively affects the pool of VSELs in adult tissues and explains the positive effect of CR on longevity.
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Gianluca D’Ippolito, Sylma Diabira, Guy A. Howard et al. · Journal of Cell Science · 2004 · 660 citations
Maternal imprinting at the H19–Igf2 locus maintains adult haematopoietic stem cell quiescence
Aparna Venkatraman, Xi He, Joanne L. Thorvaldsen et al. · Nature · 2013 · 293 citations
Life Sciences, Genetics, Hematology +16