Inductor

Origin of MSCs

Steps

Time

Percentage of differentiation reported

Technique used to demonstrate differentiation

Functionality demonstration

Reference

β-Me

Adult human bone marrow

Pre-induction in DMEM/SFB medium 20% and β-Me 1 mM for 24 h. Subsequent induction with β-Me 10 mM.

5 hours

50% demonstrated by morphological changes of neuronal nature (cytoplasm contraction, neurite extension, secondary branching).

Neuronal morphology was observed under a microscope.Increased expression of NF-M and NSE by RT-PCR.Immunostaining for NSE.

No

[54]

β-Me and RA.

Adult human bone marrow

Pre-induction in DMEM/SFB medium 20%, β-Me 10−3 M and RA 5 × 10−7 M per 24 h. Subsequent induction by serum depletion.

5 hours

98% demonstrated by positive immunofluorescence for NeuN and β-tubulin III.

Neuronal morphology was observed under a microscope.Expression of Novo de Tau and NF-H and increased expression of NSE and NeuN by RT-PCR.Increase nestin, NSE, NeuN, and Tuj-1 post-induction by WB.Immunostaining for NSE, NeuN, and Tuj1.

Presence of Na+ current and K+ post-treatment current demonstrated by Patch-clamp. Increase intracellular Ca2+ concentration when challenged with glutamate or potassium (K+).

[56]

β-Me

Adipose tissue of adult humans

Pre-induction in DMEM/SFB medium 20% and β-Me 1 mM for 24 h. Subsequent induction with β-Me 10 mM.

9 hours

70% demonstrated by morphological changes of neuronal nature.

Neuronal morphology was observed under a microscope.Increased expression of NSE, NeuN, and nestin by RT-PCR.Immunostaining for NSE.Increase in NSE per WB.

No

[55]

β-Me

The bone marrow of adult Sprague Dawley rats.

Pre-induction in DMEM/SFB medium 20% and β-Me 1 mM for 24 h. Subsequent induction with β-Me 10 mM.

3 hours

40% demonstrated by morphological changes of neuronal nature.

Neuronal morphology was observed under a microscope.Increased expression of Map2, Nefl, Tau, and Nestin by RT-PCR.Positive immunostaining for nestin, tuj1, Nef, and Flk.

No

[57]

β-Me

The bone marrow of adult Sprague Dawley rats

Pre-induction in DMEM/SFB medium 20% and β-Me 1 mM for 24 h. Subsequent induction with β-Me 5 mM.

5 hours

70% demonstrated by morphological changes of neuronal nature.

Neuronal morphology was observed under a microscope. Increase in NSE and nestin and decrease in Notch1 and Hes1 by WBImmunostaining for NSE.

No

[7]