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. 2011 Oct 17;14(1):145–155. doi: 10.1038/aja.2011.79

Table 1. Application of stem cells for the therapy of erectile dysfunction.

SCs type SCs form Model system Study duration Functional results Histology and molecular results
Rat BMSCs102 Cell (gene modified with eNOS) Aged rats 3 weeks Enhanced ICP during CN electrostimulation. Better enhancement when combined with eNOS gene therapy Enhanced eNOS expression, and cGMP levels. Transplanted cells exhibited ECs and SMCs markers
Human BMSC103 Cell Young adult rats 2 weeks No functional testing. Transplanted cells exhibited ECs and SMCs markers
Rat BMSCs106 Cell (isolated by p75 NGF receptor) Young adult rats with CN crush 4 weeks Enhanced ICP during CN electrostimulation. Better enhancement for p75-derived BMSCs p75-derived BMSCs secreted significantly more basic NGF than control group
Rat BMSCs107, 109 Cell (gene modified with VEGF) Young adult rats with DM I 4 weeks Enhanced ICP during CN electrostimulation. Better enhancement when combined with VEGF gene therapy Increased content of smooth muscle and endothelium in corporal cavernosum. Transplanted cells exhibited ECs and SMCs markers
Rat MDSCs115 Cell Young adult rats with CN transaction 2 weeks, 4 weeks Enhanced ICP during CN electrostimulation Increased percent area of PGP 9.5 staining
Mouse MDSCs78 Cell Young adult rats and aged rats 2 weeks, 4 weeks Enhanced ICP during CN electrostimulation in aged rats (2 weeks) and young adult rats (4 weeks) Increased content of smooth muscle in corporal cavernosum. Transplanted cells exhibited SMCs markers
Rabbit MDSC114 ACCMs seeded with MDSCs Young adult rabbits 2 months, 4 months, 6 months No functional testing Cells expressing ECs and SMCs markers and better arranged growth were prevalent
Rat EPCs132 Cell (gene modified with VEGF) Young adult rats with DM I 3 weeks Enhanced ICP during CN electrostimulation Enhanced neovascularisation in the corpora cavernosum. Transplanted cells exhibited ECs markers
Human UCBSCs 134 Cell Senior human with DM II 11 months Regained morning erections in some patients. Increased rigidity, but was insufficient for penetration No relevant testing
Rat ADSCs123 Cell Young adult rats 4 weeks No functional testing Injected ADSCs were localized to the sinusoid endothelium. Some Transplanted cells exhibited ECs markers
Rat ADSCs126 Cell Young adult rats with hyperlipid-emia 4 weeks Enhanced ICP during CN electrostimulation Increased content of smooth muscle and endothelium in corporal cavernosum, and nNOS-positive nerve fibres in penile dorsal nerves
Rat ADSCs127 Cell Adult ZDF rats with DM II 4 weeks Enhanced ICP during CN electrostimulation Increased nNOS staining area in penile dorsal nerves. Inhibition of apoptosis in corpus cavernosum
Rat ADSCs129 Cell and cell lysate Young adult rats with CN crush 4 weeks Enhanced ICP during CN electrostimulation Increased content of smooth muscle in corporal cavernosum, and nNOS-positive nerve fibres in penile dorsal nerves. Inhibition of fibrosis and apoptosis
Human fetal NCSCs137 Cell Young adult rats 2 weeks No functional testing Transplanted cells exhibited ECs and SMCs markers
Rat fetal BDSCs136 Cell Young adult rats 6 weeks No functional testing Transplanted cells exhibited SMCs markers or VEGF
Rat GRPCs140 Cell Young adult rats with spinal cord injury 12 weeks Preserved full and partial erectile events per 24 h GRPCs survived, differentiated and formed extensive transplants that were well integrated with host tissue
Rat neural ESCs141 Cell Young adult rats with CN crush 12 weeks Enhanced ICP during CN electrostimulation Increased neurofilament staining in the MPG and penile dorsal nerves. Improved morphological characteristics of nerve fibres in the corpora cavernosum

Abbreviations: ACCMs, acellular corporal collagen matrices; ADSCs, adipose tissue derived stem cells; BDSCs, brain-derived stem cells; BMSCs, bone marrow mesenchymal stem cells; CN, cavernous nerve; DM I, diabetes mellitus type I; DM II, diabetes mellitus type 2; ECs, endothelial cells; eNOS, endothelial nitric oxide synthase; EPCs, endothelial precursor stem cells; ESCs, embryonic stem cells; GRPCs, glial restricted progenitor cells; ICP, intracavernous pressure; MDSCs, muscle-derived stem cells; MPG, major pelvic ganglia; NCSCs, neural crest stem cells; nNOS, neuronal nitric oxide synthase; SCs, stem cells; SMCs, smooth muscle cells; UCBSCs, umbilical cord blood stem cells. PGP9.5, protein gene product 9.5; NGF, nerve growth factor; VEGF, vascular endothelial growth factor; ZDF, Zucker diabetic fatty.