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Age-related changes in Drosophila midgut are associated with PVF2, a PDGF/VEGF-like growth factor.
- Source :
-
Aging cell [Aging Cell] 2008 Jun; Vol. 7 (3), pp. 318-34. Date of Electronic Publication: 2008 Feb 13. - Publication Year :
- 2008
-
Abstract
- Age-associated changes in stem cell populations have been implicated in age-related diseases, including cancer. However, little is known about the underlying molecular mechanisms that link aging to the modulation of adult stem cell populations. Drosophila midgut is an excellent model system for the study of stem cell renewal and aging. Here we describe an age-related increase in the number and activity of intestinal stem cells (ISCs) and progenitor cells in Drosophila midgut. We determined that oxidative stress, induced by paraquat treatment or loss of catalase function, mimicked the changes associated with aging in the midgut. Furthermore, we discovered an age-related increase in the expression of PVF2, a Drosophila homologue of human PDGF/VEGF, which was associated with and required for the age-related changes in midgut ISCs and progenitor cell populations. Taken together, our findings suggest that PDGF/VEGF may play a central role in age-related changes in ISCs and progenitor cell populations, which may contribute to aging and the development of cancer stem cells.
- Subjects :
- Animals
Catalase physiology
Cell Differentiation physiology
Drosophila melanogaster cytology
Immunochemistry
Intestines cytology
Intestines physiology
Oxidative Stress physiology
RNA genetics
Reverse Transcriptase Polymerase Chain Reaction
Stem Cells cytology
Stem Cells physiology
Vascular Endothelial Growth Factors genetics
Cellular Senescence physiology
Drosophila melanogaster physiology
Vascular Endothelial Growth Factors physiology
Subjects
Details
- Language :
- English
- ISSN :
- 1474-9726
- Volume :
- 7
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Aging cell
- Publication Type :
- Academic Journal
- Accession number :
- 18284659
- Full Text :
- https://doi.org/10.1111/j.1474-9726.2008.00380.x