TY - JOUR
T1 - Platelet‐derived biomaterials exert chondroprotective and chondroregenerative effects on diabetes mellitus‐induced intervertebral disc degeneration
AU - Lo, Wen Cheng
AU - Chang, Chun Chao
AU - Chan, Chun Hao
AU - Singh, Abhinay Kumar
AU - Deng, Yue Hua
AU - Lin, Chia Ying
AU - Tsao, Wen
AU - Chien, Shaw Ting
AU - Lin, Chang Hsien
AU - Deng, Win Ping
N1 - Funding Information:
Funding: This research was funded by the Taiwan Ministry of Science and Technology [MOST 108‐ 2221‐E‐038‐014] and [MOST 110‐2314‐B‐038‐026], Taipei Medical University [TMU 108‐5601‐004‐ 111] and the Stem Cell Research Center, College of Oral Medicine, Taipei Medical University, Tai‐ wan.
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/10
Y1 - 2021/10
N2 - Complications of diabetes mellitus (DM) range from acute to chronic conditions, leading to multiorgan disorders such as nephropathy, retinopathy, and neuropathy. However, little is known about the influence of DM on intervertebral disc degeneration (IVDD). Moreover, traditional surgical outcomes in DM patients have been found poor, and to date, no definitive alternative treatment exists for DM‐induced IVDD. Recently, among various novel approaches in regenerative medicine, the concentrated platelet‐derived biomaterials (PDB), which is comprised of transforming growth factor‐β1 (TGF‐β1), platelet‐derived growth factor (PDGF), etc., have been reported as safe, biocompatible, and efficacious alternatives for various disorders. Therefore, we initially investigated the correlations between DM and IVDD, through establishing in vitro and in vivo DM models, and further evaluated the therapeutic effects of PDB in this comorbid pathology. In vitro model was established by culturing immortalized human nucleus pulposus cells (ihNPs) in high‐glucose medium, whereas in vivo DM model was developed by administering streptozotocin, nicotinamide and high‐fat diet to the mice. Our results revealed that DM deteriorates both ihNPs and IVD tissues, by elevating reactive oxygen species (ROS)‐induced oxidative stress, inhibiting chondrogenic markers and disc height. Contrarily, PDB ameliorated IVDD by restoring cellular growth, chondrogenic markers and disc height, possibly through suppressing ROS levels. These data imply that PDB may serve as a potential chondroprotective and chondroregenerative candidate for DM‐induced IVDD.
AB - Complications of diabetes mellitus (DM) range from acute to chronic conditions, leading to multiorgan disorders such as nephropathy, retinopathy, and neuropathy. However, little is known about the influence of DM on intervertebral disc degeneration (IVDD). Moreover, traditional surgical outcomes in DM patients have been found poor, and to date, no definitive alternative treatment exists for DM‐induced IVDD. Recently, among various novel approaches in regenerative medicine, the concentrated platelet‐derived biomaterials (PDB), which is comprised of transforming growth factor‐β1 (TGF‐β1), platelet‐derived growth factor (PDGF), etc., have been reported as safe, biocompatible, and efficacious alternatives for various disorders. Therefore, we initially investigated the correlations between DM and IVDD, through establishing in vitro and in vivo DM models, and further evaluated the therapeutic effects of PDB in this comorbid pathology. In vitro model was established by culturing immortalized human nucleus pulposus cells (ihNPs) in high‐glucose medium, whereas in vivo DM model was developed by administering streptozotocin, nicotinamide and high‐fat diet to the mice. Our results revealed that DM deteriorates both ihNPs and IVD tissues, by elevating reactive oxygen species (ROS)‐induced oxidative stress, inhibiting chondrogenic markers and disc height. Contrarily, PDB ameliorated IVDD by restoring cellular growth, chondrogenic markers and disc height, possibly through suppressing ROS levels. These data imply that PDB may serve as a potential chondroprotective and chondroregenerative candidate for DM‐induced IVDD.
KW - Diabetes mellitus (DM)
KW - Hyperglycemia
KW - Immortalized human nucleus pulposus cells (ihNPs)
KW - Intervertebral disc degeneration (IVDD)
KW - Platelet‐derived biomaterials (PDB)
KW - Reactive oxygen species (ROS)
UR - http://www.scopus.com/inward/record.url?scp=85117230827&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85117230827&partnerID=8YFLogxK
U2 - 10.3390/life11101054
DO - 10.3390/life11101054
M3 - Article
AN - SCOPUS:85117230827
SN - 0024-3019
VL - 11
JO - Life
JF - Life
IS - 10
M1 - 1054
ER -