2020
DOI: 10.1007/s12015-020-09964-x
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Increased Exhaustion of the Subchondral Bone-Derived Mesenchymal Stem/ Stromal Cells in Primary Versus Dysplastic Osteoarthritis

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Cited by 15 publications
(29 citation statements)
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“…It appears that the exhaustion of physiologically occurring MSCs in patients with primary osteoarthritis occurs. In biomechanical joint damage, subchondral bone populations of MSCs are not impaired [ 54 , 55 , 56 ]. It is also important to establish the ability to proliferate and differentiate, which are key processes in the harvesting of MSCs.…”
Section: Mesenchymal Stem/stromal Cells—origin Cellular and Molecular Characteristics And Signaling Pathways Involved In Differentiationmentioning
confidence: 99%
“…It appears that the exhaustion of physiologically occurring MSCs in patients with primary osteoarthritis occurs. In biomechanical joint damage, subchondral bone populations of MSCs are not impaired [ 54 , 55 , 56 ]. It is also important to establish the ability to proliferate and differentiate, which are key processes in the harvesting of MSCs.…”
Section: Mesenchymal Stem/stromal Cells—origin Cellular and Molecular Characteristics And Signaling Pathways Involved In Differentiationmentioning
confidence: 99%
“…In humans, the use of autologous or allogeneic cells that are most commonly derived from bone marrow or adipose tissue has reshaped the treatment of debilitating age-associated or injury-inflicted joint disorders. However, there remains substantial concern for the use of autologous cell therapies in patients who already have degenerative disorders, as the regenerative potential of the endogenous MSCs might be impaired or exhausted [ 4 , 5 , 6 , 7 , 8 ]. Degenerative comorbidities and the increasing age of the donor might also have an impact on the quantity of obtainable MSCs [ 6 ].…”
Section: Introductionmentioning
confidence: 99%
“…In a recent study, Klemen Čamernik et al provided new scientific knowledge for the pathophysiological mechanisms of primary osteoarthritis (OA) in relation to mesenchymal stromal cells (MSCs) features. The authors reported that the exhaustion of MSCs may be implicated in the pathogenesis of OA (1). As evoked by the authors, medicinal approaches that target exhausted or impaired MSCs might provide new promise for future treatments.…”
mentioning
confidence: 98%
“…These subchondral MSCs were exhausted and presented altered differential potential. Indeed, they showed lower viability, altered osteogenesis and chondrogenesis as well as lower expression of the leptin receptor (LepR) [1]. As known, LepR is a marker of quiescent MSCs that proliferate regenerate bone after injury [11].…”
mentioning
confidence: 99%
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