Table 1.
BM Cells | Target Disease | Differentiation Potential | Phenotype | Telomerase | Senescence Tendency | References |
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EPCs | Retinal Ischemia, Parkinson’s Disease, Malignant Tumors, Chronic Obstructive Pulmonary Disease, Ischemic Stroke, Traumatic Brain Injury, Alzheimer’s Disease | CD34+, CD31+, AC133+, VEGFR2+, Tle-2+ | Endothelial Cells | Positive | PD6 until 7–8 days, with Senescence augmented by estrogen or SDF-1 treatment | Asahara et al., 1997, 1999. Takahashi et al., 1999. Gehling et al., 2000. Lin et al., 2000. Heissig et al., 2002. Imanishi et al., 2006. Ingram et al., 2006. Kocher et al., 2006. Rustemeyer et al., 2006. Lapergue et al., 2007. McCarty, 2009. Li Carzi et al., 2010. Reimers et al., 2010. Zheng et al., 2010. Andres et al., 2011. Hesa and Allan, 2011. Huertas and Palange, 2011. Jiang and chen, 2011. Kong et al., 2011. |
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MSCs | Malignant Tumors and cancer | Not Addressed | OCA cells | N/A | Mean CPDL is about 38 PDs at passage 15 | Bruder et al., 1997. Ozawa et al., 2005. Sordi and Piemonti, 2010. Hamada et al., 2011. |
Inflamation, Autoimmune, Asthma | Not Addressed | OCA cells | N/A | Lose MDP at 19–22 PDs. CPDL is around 22–23 in 80 days of culture | Banfi et al., 2000. Parekkadan et al., 2008, Nemeth et al., 2010. | |
Neurological Damage and Regeneration (Stroke, Alzheimec, Parkinson, Tramatic Brain Injury, Spinal Cord Injury) | Not Addressed | OCA cells | N/A | Lose MDP at 19–22 PDs. CPDL is around 22–23 in 80 days of culture | Muraglia et al., 2000. Zwart et al., 2009. Bakhtiary et al., 2010. Cheng et al., 2010. Lee et al., 2010. Osaka 2010. Khoo et al., 2011. Zhou, 2011. | |
Cardio-Related Disease (i.e., Ischemic Cardiomyopathy, Myocardial Infarction) | SH2+, SH3+, CD29+, CD44+, CD14−, CD34− and CD45− | OCA cells | Negative | CPDL is around 18 PDs, at about 80 days | Zimmerman et al., 2003. Wang et al., 2010. Liang et al., 2011. | |
Inflamatory Bowel | Not Addressed | OCA cells | N/A | CPDL is 15 PDs of about 40 days of culture | Kobune et al., 2003. Ko et al., 2010. | |
Multiple Sclerosis and Liver Regeneration | Not Addressed | OCA cells | N/A | CPDL in serum-deprived hMSCs is about 9 PDs at passage 10. CPDL for control hMSCs is about 7 PDs at passage 8 | Pochampally et al., 2004. Witherick et al., 2010., Sokal 2011. | |
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hTERT-MSCs | Cerebral Ischemia and Spinal Cord Injury | Not Addressed | OCA cells | N/A | PP remains until 80 PDs of about 400 days of culture | Kobune et al., 2003. Honma et al., 2006. |
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HSCs | Alzheimer’s Disease, Traumatic Brain Injury, Myeloid Leukaemia, Sickle Cell Anemia, Cutaneous Repair | Blood cells | CD34+, CXCR4+ | Positive | Up for debate, thought to be dysfunctional in aging HSCs, but even reduced telemere expression neither shorten telemere nor limit PP | Lapidot and Kollet, 2005. Nervi et al., 2006. Papayannopoulou and Scadden, 2008. Sanchez-Ramos et al., 2006. Zimmerman and Martens, 2008. Geiger and Rudolph, 2009. Guo et al., 2009. Lapidot and Kollet, 2010. Drukala et al., 2011. Klinakis et al., 2011. McNeer et al., 2011. |
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VSEL Cells | Tissue Rejuvertation, Stroke, Myocardial Infarctions, Diabetes, Cutaneous Repair | SSEA-1+, Oct-4+, Nanog+, Rex-1+, Sca-1+, CD45− | Three germ lineages | Positive | Expand for about 7 PDs (personal communication with author) | Kucia et al., 2006b, 2007. Ratajczak et al., 2006. Zuba-Surma et al., 2005. Paczkowska et al., 2009. Shin et al., 2009. Wojakowski et al., 2009. Hocking et al. 2010. Huang et al., 2010. Shin et al., 2010. Drukala et al., 2011. Sovalat et al., 2011. Wojakowski et al., 2011. |
OCA cells: osteogenic, chondrogenic and adipogenic cells; PDs: population doublings; CPDL: cumulative population doubling level; PP: proliferation potential; MDP: multiple lineages differentiate potential; Not Addressed: authors did not describe this topic in their study; Negative/positive: the activity of telomerase is negative or positive.