Evaluate the optimal cellular ratio of human mesenchymal stem cells and primary chondrocytes for cartilage formation in an in vitro culture and in vivo nude mice model.
ID
Source
Brief title
Condition
- Tendon, ligament and cartilage disorders
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
Primary endpoint of this study will be after 6 weeks of in vitro culture or in
vivo survival of the co-cultured chondrocytes and mesenchymal stem cells. At
this time point we will analyze the ideal ratio of these cells for cartilage
formation based on alcian blue staining, collagen propeptide I and II
determination, safranin O staining and aggrecan ELISA.
Secondary outcome
-
Background summary
Trauma and disease of knee joints frequently involve structural damage to
articular cartilage.
Since 15 years autologous chondrocyte implantation (ACI) shows satisfactory
results for the restoration of focal cartilage lesions. However, the necessary
in vitro expansion of the harvested chondrocytes induces cellular
dedifferentiation, resulting in diminished cellular quality. Hendriks et al
combined primary bovine chondrocytes and human mesenchymal stem cells in an in
vitro co-culture system. This combination led to an increase of cartilage
specific matrix constituents at varying cell-cell ratios and, therefore,
introduces the possibility to investigate the potential of a single surgery
therapy for focal cartilage lesions.
This study will combine human mesenchymal stem cells and human primary
chondrocytes from the same donor at different ratios to evaluate the effect on
cartilage formation. We will obtain our cells from patients admitted to
reconstructive anterior cruciate ligament (ACL) surgery.
Study objective
Evaluate the optimal cellular ratio of human mesenchymal stem cells and primary
chondrocytes for cartilage formation in an in vitro culture and in vivo nude
mice model.
Study design
Patients admitted to ACL reconstructive surgery will be informed about this
study by the treating surgeon and asked for approval to obtain bone marrow
during the operation and the use of their cells for laboratory cartilage
research. After approval we will combine the primary chondrocytes and
mesenchymal stem cells at different ratios and culture them in an in vitro and
in vivo model for six weeks followed by immunohistochemical, histological and
biochemical analysis on cartilage formation.
Study burden and risks
We expect, although cannot proof this because of lack of experience and
available data, that the additional surgical procedure (aspiration of bone
marrow before drilling the femoral hole) will not have any negative influence
on surgical outcome or patient recovery.
Heidelberglaan 100
3584CX Utrecht
NL
Heidelberglaan 100
3584CX Utrecht
NL
Listed location countries
Age
Inclusion criteria
-Male and female patients over 18 years of age
-Patients with a ruptured ACL admitted to ACL reconstructive surgery
Exclusion criteria
-Patients over 40 years of age
-Patients with generalized cartilage degeneration
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL21170.041.08 |