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. Author manuscript; available in PMC: 2021 Apr 16.
Published in final edited form as: Neuroimmunol Neuroinflamm. 2021 Mar 21;8:53–63. doi: 10.20517/2347-8659.2020.34

Table 2.

Effects of BMP treatment on neuronal and non-neuronal cells in SCI in in vitro models

BMP signaling component Treatment Outcomes Ref.
BMP ligands BMP7 BMP7 inhibited tumor necrosis factor α-mediated oligodendrocyte death [56]
BMP7 BMP7 inhibited glutamate induced neuronal cell death [24]
BMP4 In vitro culture of NSCs in the presence of BMP4 resulted in amelioration of oligodendrocyte differentiation and increase in astrocyte differentiation. Smad1 and 5 were activated in response to BMP4 treatment of NSCs [25]
BMP7 Noggin expressing OPCs treated with BMP7 showed less astrocytic differentiation [16]
BMP antagonists Noggin Noggin treatment reduced astrocyte numbers. Inhibition of BMP4 using noggin attenuated differentiation of NSCs into astrocytes [37]
Noggin Noggin treatment of OPCs partially reduced astrocytic differentiation [40]
Noggin Noggin treatment reduced differentiation of OPCs into astrocytes in astrocyte conditioning media. p-Smad1, 5, and 8 levels were increased in OPCs in astrocyte conditioning media compared to control. OPCs cultured in astrocyte conditioning media predominantly differentiated into astrocytes [36]
Noggin and LDN193189 Treatment attenuated BMP4 induced activation of caspase-3 for cell death in neurons and oligodendrocytes post-SCI [57]
Noggin Noggin treatment reduced astrocytic differentiation and increased the differentiation of NSCs into oligodendrocytes [25]

BMP: bone morphogenic protein; SCI: spinal cord injury; OPCs: oligodendrocyte precursor cells; NSCs: neural stem cells