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. 2021 Mar 29;22(7):3519. doi: 10.3390/ijms22073519

Table 3.

Recent studies related to the homing capabilities of MSCs into the IVD.

Species Study Type Cell Types Outcomes References
Human in vitro BM MSCs Growth factors and chemokines such as IGF-1, PDGF-AB, RANTES, and SDF-1 showed a chemoattractive effect on MSCs. [95]
Bovine IVDs and human MSCs ex vivo BM MSCs An intradiscal injectable hydrogel-based on hyaluronan-poly(N-isopropylacrylamide) and supplemented with SDF-1 showed a chemoattractive effect on MSCs. [97]
Bovine IVDs and human MSCs ex vivo BM MSCs The concentration of RANTES was significantly elevated in the medium of induced degenerated IVDs; RANTES may be a key chemoattractant for MSCs in the IVD. [98]
Bovine IVDs and human MSCs ex vivo BM MSCs MSC subpopulations positive for CD146 were associated with a greater homing potential but produced a weaker regenerative response than CD146-negative MSCs. [99]
Murine model with human MPSCs in vivo Umbilical cord blood MPSCs Intravenously injected MSCs showed limited ability to home into a degenerated IVD, but they upregulated GAG and ACAN. [100]
Murine in vivo BM MSCs Intravenously injected MSCs significantly decreased IVD herniation and induced an immunomodulatory effect. [101]
Murine in vivo BM MSCs Only a limited number of intravenously injected MSCs migrated to a degenerated IVD. However, the more serious the injury, the more cells were recruited. [92]
Bovine IVDs and human MSCs ex vivo BM MSCs Greater MSC homing occurred with degenerated IVDs than healthy samples, and IGF-1-transduced MSCs significantly increased the proteoglycan synthesis. [93]
Bovine IVDs and human MSCs ex vivo BM MSCs MSCs seeded on the endplate’s surface of nucleotomized IVDs migrated into the NP and stimulated ECM production and growth factors. [104]
Bovine and human ex vivo BM MSCs Homed MSCs increased the fraction of Tie2-positive IVD cells, enhanced IVD cell proliferation, and reduced the fraction of dead cells in the IVD. [105]

Abbreviations: IVD = intervertebral disc, BM = bone marrow, MSC = mesenchymal stromal cells, MPSC = multipotent stem cells, IGF-1 = insulin-like growth factor 1, PDGF-AB = platelet-derived growth factor -AB, SDF-1 = stromal cell-derived factor 1, CD146 = cluster of differentiation 146, GAG = glycosaminoglycan, ACAN = aggrecan, ECM = extracellular matrix, and Tie2 = angiopoietin-1 receptor.