Insert INTO PMID_Summary(PMID,summaryText,IPAddress,dtCreated) VALUES (21595512, '** The study investigates how neuropeptide Y (NPY) and its Y5 receptor (Y5R) affect the growth of bone marrow cells from rats of different ages, revealing that aging cells have reduced proliferation abilities. ** NPY was found to enhance the growth of all age groups of bone marrow cells, but the effectiveness was diminished in older cells due to lower Y5R expression. ** By increasing Y5R expression in aged bone marrow cells, researchers were able to significantly boost their proliferation, suggesting a potential method to rejuvenate aging bone marrow. **','18.191.171.10',now()) Neuropeptide y and neuropeptide y y5 receptor interaction restores impaired growth potential of aging bone marrow stromal cells. | LitMetric

AI Article Synopsis

  • The study investigates how neuropeptide Y (NPY) and its Y5 receptor (Y5R) affect the growth of bone marrow cells from rats of different ages, revealing that aging cells have reduced proliferation abilities.
  • NPY was found to enhance the growth of all age groups of bone marrow cells, but the effectiveness was diminished in older cells due to lower Y5R expression.
  • By increasing Y5R expression in aged bone marrow cells, researchers were able to significantly boost their proliferation, suggesting a potential method to rejuvenate aging bone marrow.

Article Abstract

Abstract improved growth characteristics of the aging bone marrow cells subsequent to neuropeptide Y (NPY)/neuropeptide Y Y5 receptor (NPY Y5R) ligand-receptor interaction. Bone marrow cells were isolated from neonatal (2-3 weeks), young (8-12 weeks), and old (24-28 months) rats on the basis of their preferential adherence to plastic surface. After culturing the cells at initial seeding density of 1×10(4) cells/cm(2), we found that the proliferation potential of bone marrow cells declined with age. Real-time polymerase chain reaction (PCR) and Western blotting showed that bone marrow cells in different age groups constitutively expressed NPY and NPY receptor subtypes (Y1R, Y2R, and Y5R). However, NPY and Y5R expression increased by more than 130-fold and decreased by 28-fold, respectively, in old bone marrow cells as compared to young bone marrow cells. NPY (10 nM) stimulated the proliferation of all bone marrow cells age groups, and their proliferation was blocked by Y5R antagonist. However, the pro-proliferative effect of NPY on old bone marrow cells was weaker than other cell groups due to lower Y5R expression. Y5R gene transfection of old bone marrow cells with subsequent NPY(3-36) (10 nM) treatment significantly increased proliferation of old bone marrow cells (>56%) as compared to green fluorescence protein-transfected control old bone marrow cells. Stimulation of old bone marrow cells by NPY treatment rejuvenated the growth characteristics of aging bone marrow cells as a result of Y5R overexpression.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3157931PMC
http://dx.doi.org/10.1089/rej.2010.1129DOI Listing

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