| Full text | |
| Author(s): |
Nakajima, Karina
[1]
;
Crisma, Amanda R.
[2]
;
Silva, Graziela B.
[1]
;
Rogero, Marcelo M.
[3]
;
Fock, Ricardo A.
[1]
;
Borelli, Primavera
[1]
Total Authors: 6
|
| Affiliation: | [1] Univ Sao Paulo, Expt Hematol Lab, Dept Clin & Toxicol Anal, Fac Pharmaceut Sci, Sao Paulo - Brazil
[2] Univ Sao Paulo, Dept Physiol & Biophys, Inst Biomed Sci, Cellular Physiol Lab, Sao Paulo - Brazil
[3] Univ Sao Paulo, Sch Publ Hlth, Dept Nutr, Sao Paulo - Brazil
Total Affiliations: 3
|
| Document type: | Journal article |
| Source: | NUTRITION; v. 30, n. 1, p. 82-89, JAN 2014. |
| Web of Science Citations: | 11 |
| Abstract | |
Objective: Protein malnutrition (PM) often is associated with changes in bone marrow (BM) microenvironment leading to an impaired hematopoiesis; however, the mechanism involved is poorly understood. The aim of this study was to compare the cell cycle progression of hematopoietic stem cells (HSC) and hematopoietic progenitor cells (HPC) and evaluate the cell cycle signaling in malnourished mice to assess the mechanism of cell cycle arrest. Methods: C57B1/6J mice were randomly assigned in control and malnourished groups receiving normoproteic and hypoproteic diets (12% and 2% protein, respectively) over a 5-wk period. Nutritional and hematologic parameters were assessed and BM immunophenotypic analysis was performed. Cell cycle of HPC (Lin(-)) and HSC (Lin(-)Sca-1(+)c-Kit(+)) were evaluated after 6 h of in vivo 5-bromo-2'-deoxyuridine (BrDU) incorporation. Cell cycle regulatory protein expression of HPC was assessed by Western blot. Results: Malnourished mice showed lower levels of serum protein, albumin, glucose, insulin-like growth factor-1, insulin, and higher levels of serum corticosterone. PM also caused a reduction of BM myeloid compartment resulting in anemia and leukopenia. After 6 h of BrDU incorporation, malnourished mice showed G0-G1 arrest of HPC without changes of HSC proliferation kinetics. HPC of malnourished mice showed reduced expression of proteins that induce cell cycle (cyclin D1, cyclin E, pRb, PCNA, Cdc25a, Cdk2, and Cdk4) and increased expression of inhibitory proteins (p21 and p27) with no significant difference in p53 expression. Conclusion: PM suppressed cell cycle progression mainly of HPC. This occurred via cyclin D1 downregulation and p21/p27 overexpression attesting that BM microenvironment commitment observed in PM is affecting cell interactions compromising cell proliferation. (C) 2014 Elsevier Inc. All rights reserved. (AU) | |