Basic & Clinical Medicine ›› 2017, Vol. 37 ›› Issue (1): 13-18.

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Sustained hypoxia promotes the proliferation and reduces apoptosis of rabbit urine derived stem cells

  

  • Received:2016-03-30 Revised:2016-05-28 Online:2017-01-05 Published:2016-12-30

Abstract: Objective To investigate the effects of hypoxia on the cell proliferation, apoptosis and secretion of rabbit urine derived stem cells (rUSCs);Methods rUSCs were isolated and cultured with oxygen concentration at 20 % and 3 %, respectively. To observe the morphological changes of rUSCs in different culture conditions continuously; The growth curves under different culture conditions were drawn respectively;Antibody detection of factor secretion was performed;The cell cycle and the apoptosis were analyzed by flow cytometry. Results Single, small, compact “rice-grain” like cells were observed on day 6, after cultured in different oxygen concentration,the cells in normoxia group appeared like "spindle", the cells in hypoxia group changed into " pebble" like; The growth curves of two groups showed a "S" shape, but the cells in hypoxia group had a faster growth speed compared with normoxia group (P <0.01 resp.); Compared with normoxia group, the paracrine effect in hypoxia group had an increased expression level , and an increased variety ; Less cells were arrested at G0/G1 phase under hypoxia as compared with that in normoxia group(71.82%±8.86% and 91.73%±1.35%, resp.) (P<0.05), while the cell numbers at S phase increased in hypoxia group are comparied with that of normoxia group(18.77%±3.87% and 3.48%±0.73%, resp.) (P<0.01); The apoptosis rate of normoxia group(3.24%±0.38% ) was significantly higher than that of hypoxia group by flow cytometry (0.43%±0.05%) (P<0.001); and the apoptosis rate of normoxia group(4.27%± 0.48% ) was significantly higher than that of hypoxia group by Hoechst(1.37%± 0.33%)(P<0.01). Conclusion It is demonstrated that culture at 3% O2 could enhance cell proliferation and reduce apoptosis of rUSCs.

Key words: rabbit urine derived stem cells, hypoxia, cell proliferation, cell apoptosis

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