Optimization of isolation and culture of LinSca-1cardiac stem cells from newborn mice.
- Author:
Duan-Duan LI
1
;
Shan-Hui SHI
1
;
Mi ZHOU
1
;
Xiu-Xia MA
1
;
Jian-Zhong GAO
2
;
Ya-Qiong ZHANG
3
;
Li-Wen YANG
4
;
Lin ZUO
5
Author Information
1. Department of Physiology, Basic Medical College, Shanxi Medical University, Taiyuan 030001, China.
2. Department of Pathology, the First Affiliated Hospital, Shanxi Medical University, Taiyuan 030001, China.
3. The First Affiliated Hospital, Shanxi Medical University, Taiyuan 030001, China.
4. The Second Affiliated Hospital, Shanxi Medical University, Taiyuan 030001, China.
5. Department of Physiology, Basic Medical College, Shanxi Medical University, Taiyuan 030001, China. zuol1505@126.com.
- Publication Type:Journal Article
- From:
Acta Physiologica Sinica
2017;69(4):477-484
- CountryChina
- Language:Chinese
-
Abstract:
Cardiac stem cells (CSCs) transplantation has been recognized to be effective on the treatment of myocardial infarction (MI), but some techniques still need to be developed in the isolation and culture of CSCs, which is the key problem restricting the clinical application of CSCs. This study was focused on the isolation of Lin(lineage-negative) Sca-1(stem cell antigen-1-positive) CSCs from newborn C57BL/6J mice (0-3 d) by mixed enzymatic-explant isolation in combination with immunomagnetic separation. The digesting time, digesting frequency, incubation temperature, stirring speed, centrifugation time and rotational speed were strictly controlled in the experiment. In order to increase the survival rate of CSCs, the medium changing time and manner were optimized in primary CSCs culture. The percentages of Sca-1cells in primary and passage cells were detected by flow cytometry and immunofluorescence staining. The results showed that: (1) the proportion of LinSca-1cells within the collected cells could be as high as (85.03 ± 5.60)% after isolation and purification; (2) In vitro culture of LinSca-1CSCs grew into spheres on the 5day, and over the whole bottom of the dish on the 7day. The growth curve showed that the cells were in logarithmic growth phase on the 3day; (3) Immunofluorescence staining data showed that the expression of Sca-1, the CSCs membrane-specific marker, was decreased after subculture, and flow cytometry data showed that the percentages of Sca-1cells were (71.82 ± 2.63)%, (58.38 ± 3.70)% and (46.19 ± 4.72)% in passage 1 (P1), P3, and P5 CSCs, respectively. The above results suggest that high purity of LinSca-1CSCs can be obtained by enzymolysis combined with immunomagnetic separation method. Moreover, the CSCs culture system is stable. In our experiment, the Sca-1CSCs isolation and culture method has been successfully established, and it is simple, stable, effective and reliable. The method can provide a stable methodological basis for the treatment of MI by LinSca-1CSCs transplantation.
