Bone marrow vs Wharton's jelly mesenchymal stem cells in experimental sepsis: a comparative study

被引:37
|
作者
Laroye, Caroline [1 ,2 ,3 ,4 ]
Boufenzer, Amir [5 ]
Jolly, Lucie [2 ,4 ,5 ]
Cunat, Lisiane [4 ,6 ]
Alauzet, Corentine [4 ,6 ]
Merlin, Jean-Louis [4 ,7 ]
Yguel, Clemence [8 ]
Bensoussan, Daniele [1 ,3 ,4 ]
Reppel, Loic [1 ,3 ,4 ]
Gibot, Sebastien [2 ,4 ,9 ]
机构
[1] CHU Nancy, Unite Therapie Cellulaire & Banque Tissus, Allee Morvan, F-54500 Vandoeuvre Les Nancy, France
[2] INSERM, UMRS 1116, Vandoeuvre Les Nancy, France
[3] CNRS, UMR 7365, F-54500 Vandoeuvre Les Nancy, France
[4] Univ Lorraine, F-54000 Nancy, France
[5] INOTREM, F-54500 Vandoeuvre Les Nancy, France
[6] EA 7300 Stress Immunite Pathogenes, F-54500 Vandoeuvre Les Nancy, France
[7] Inst Cancerol Lorraine, Unite Biol Tumeurs, Serv Biopathol, F-54500 Vandoeuvre Les Nancy, France
[8] CHRU Nancy, Lab Anat & Cytol Pathol, F-54500 Vandoeuvre Les Nancy, France
[9] CHRU Nancy, Serv Reanimat Med, Hop Cent, F-54000 Nancy, France
关键词
Mesenchymal stem cells; Tissue source; Wharton's jelly; Bone marrow; Sepsis; INTERNATIONAL CONSENSUS DEFINITIONS; STROMAL CELLS; SEPTIC SHOCK; ADIPOSE-TISSUE; MULTIPOTENT; CRYOPRESERVATION; SURVIVAL; CRITERIA; BLOOD;
D O I
10.1186/s13287-019-1295-9
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background: The use of mesenchymal stem cells (MSCs) is being extensively studied in clinical trials in the setting of various diseases including diabetes, stroke, and progressive multiple sclerosis. The unique immunomodulatory properties of MSCs also point them as a possible therapeutic tool during sepsis and septic shock, a devastating syndrome associated with 30-35% mortality. However, MSCs are not equal regarding their activity, depending on their tissue origin. Here, we aimed at comparing the in vivo properties of MSCs according to their tissue source (bone marrow (BM) versus Wharton's jelly (WJ)) in a murine cecal ligation and puncture (CLP) model of sepsis that mimics a human peritonitis. We hypothesized that MSC properties may vary depending on their tissue source in the setting of sepsis. Methods: CLP, adult, male, C57BL/6 mice were randomized in 3 groups receiving respectively 0.25 x 10(6) BM-MSCs, 0.25 x 10(6) WJ-MSCs, or 150 mu L phosphate-buffered saline (PBS) intravenously 24 h after the CLP procedure. Results: We observed that both types of MSCs regulated leukocyte trafficking and reduced organ dysfunction, while only WJ-MSCs were able to improve bacterial clearance and survival. Conclusion: This study highlights the importance to determine the most appropriate source of MSCs for a given therapeutic indication and suggests a better profile for WJ-MSCs during sepsis.
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收藏
页数:11
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