Gene expression profiling of primary fibrochondrocyte cultures in traumatic and degenerative meniscus lesions.


Journal

Journal of orthopaedic surgery (Hong Kong)
ISSN: 2309-4990
Titre abrégé: J Orthop Surg (Hong Kong)
Pays: England
ID NLM: 9440382

Informations de publication

Date de publication:
Historique:
entrez: 17 3 2021
pubmed: 18 3 2021
medline: 22 7 2021
Statut: ppublish

Résumé

This study aimed to investigate how fibroblastic and chondrocytic properties of human meniscal fibrochondrocytes are affected in culture conditions according to the type of meniscal pathology and localization, and to provide basic information for tissue-engineering studies. Primary fibrochondrocyte cultures were prepared from meniscus samples of patients who had either traumatic tear or degeneration due to osteoarthritis. Cultures were compared in terms of mRNA expression levels of COL1A1, COL2A1, COMP1, HIF1A, HIF2A, and SOX9 and secreted total collagen and sulfated sGAG levels according to the type of meniscal pathology, anatomical localization, and the number of subcultures. mRNA expression levels of COL1A1, COMP1, HIF1A, HIF2A, and SOX9 were found to be increased in subsequent subcultures in all specimens. COL1A1 mRNA expression levels of both lateral and medial menisci of patients with traumatic tear were significantly higher than in patients with degenerative pathology, indicating a more fibroblastic character. P1 subculture of lateral and P3 or further subculture of medial meniscus showed more fibroblastic characteristics in patients with degenerative pathology. Furthermore, in patients with degenerative pathology, the subcultures of the lateral meniscus (especially on the inner part) presented more chondrocytic characteristics than did those of medial meniscus. The mRNA expression levels of the cultures showed significant differences according to the anatomical localization and pathology of the meniscus, indicating distinct chondrocytic and fibroblastic features. This fundamental knowledge would help researchers to choose more efficient cell sources for cell-seeding of a meniscus scaffold, and to generate a construct resembling the original meniscus tissue.

Identifiants

pubmed: 33729061
doi: 10.1177/23094990211000168
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

23094990211000168

Auteurs

Nuri Aydın (N)

Department of Orthopaedics and Traumatology, 64298Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, Istanbul, Turkey.

Bedri Karaismailoğlu (B)

Department of Orthopaedics and Traumatology, 64298Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, Istanbul, Turkey.

Merve Alaylıoğlu (M)

Brain and Neurodegenerative Disorders Research Laboratory, Department of Medical Biology, 64298Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, Istanbul, Turkey.

Duygu Gezen-Ak (D)

Brain and Neurodegenerative Disorders Research Laboratory, Department of Medical Biology, 64298Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, Istanbul, Turkey.

Büşra Şengül (B)

Brain and Neurodegenerative Disorders Research Laboratory, Department of Medical Biology, 64298Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, Istanbul, Turkey.

Esin Candaş (E)

Brain and Neurodegenerative Disorders Research Laboratory, Department of Medical Biology, 64298Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, Istanbul, Turkey.

Selma Yılmazer (S)

Department of Medical Biology, Faculty of Medicine, 187458Altinbas University, Istanbul, Turkey.

Erdinç Dursun (E)

Brain and Neurodegenerative Disorders Research Laboratory, Department of Medical Biology, 64298Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, Istanbul, Turkey.
Department of Neuroscience, Institute of Neurological Sciences, Istanbul University-Cerrahpasa, Istanbul, Turkey.

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Classifications MeSH