Bone Marrow-Derived Mesenchymal Stem Cells Prevent the Loss of Niemann-Pick Type C Mouse Purkinje Neurons by Correcting Sphingolipid Metabolism and Increasing Sphingosine-1-phosphate

作者：Lee Hyun; Lee Jong Kil; Min Woo Kie; Bae Jae Hoon; He Xingxuan; Schuchman Edward H; Bae Jae Sung^*; Jin Hee Kyung

来源：Stem Cells, 2010, 28(4): 821-831.

DOI：10.1002/stem.401

• Niemann-Pick type C disease model
• Bone marrow-derived mesenchymal stem cells
• Purkinje neuron
• Sphingosine-1-phosphate
• Apoptosis
• Therapeutic potential

Niemann-Pick type C (NP-C) disease exhibits neuronal sphingolipid storage and cerebellar Purkinje neuron (PN) loss. Although it is clear that PNs are compromised in this disorder, it remains to be defined how neuronal lipid storage causes the PN loss. Our previous studies have shown that bone marrow-derived mesenchymal stem cells (BM-MSCs) transplantation prevent PN loss in NP-C mice. The aim of the present study was therefore to examine the neuroprotective mechanism of BM-MSCs on PNs. We found that NP-C PNs exhibit abnormal sphingolipid metabolism and defective lysosomal calcium store compared to wildtype mice PNs. BM-MSCs promote the survival of NP-C PNs by correction of the altered calcium homeostasis, restoration of the sphingolipid imbalance, as evidenced by increased sphingosine-1-phosphate levels and decreased sphingosine, and ultimately, inhibition of apoptosis pathways. These effects suggest that BM-MSCs modulate sphingolipid metabolism of endogenous NP-C PNs, resulting in their survival and improved clinical outcome in mice. STEM CELLS 2010;28:821-831

• 出版日期2010-4