TY - JOUR
T1 - Forskolin rapidly enhances neuron-like morphological change of directly induced-neuronal cells from neurofibromatosis type 1 patients
AU - Sagata, Noriaki
AU - Kano, Shin ichi
AU - Ohgidani, Masahiro
AU - Inamine, Shogo
AU - Sakai, Yasunari
AU - Kato, Hiroki
AU - Masuda, Keiji
AU - Nakahara, Takeshi
AU - Nakahara-Kido, Makiko
AU - Ohga, Shouichi
AU - Furue, Masutaka
AU - Sawa, Akira
AU - Kanba, Shigenobu
AU - Kato, Takahiro A.
N1 - Funding Information:
The authors would like to thank Ms Yuka Matsushita and Ms Aya Yamada for their technical assistance. This work was supported by Grant-in-Aid for Scientific Research on (1) Innovative Areas “Will-Dynamics” of The Ministry of Education, Culture, Sports, Science, and Technology, Japan (JP16H06403 to TAK), (2) The Japan Agency for Medical Research and Development (AMED) (“Syogaisya-Taisaku-Sogo-Kenkyu-Kaihatsu-Jigyo” JP19dk0307047 & JP19dk0307075, and “Yugo-no” JP19dm0107095 to TAK), (3) KAKENHI—the Japan Society for the Promotion of Science (“Wakate A” JP26713039 and “Kiban A” JP18H04042 to TAK, and “Wakate B” JP26860932 & JP17K16386 to NS), (4) SENSHIN Medical Research Foundation (to TAK and SK), (5) Mochida Memorial Foundation for Medical and Pharmaceutical Research (to TAK), (6) NIH R00 MH093458 (S-IK), (7) NIH RO1 MH-105660 (AS), (8) the National Institute of Mental Health MH-084018 (AS), (9) MH-094268 Silvio O. Conte center (AS), (10) MH-092443 (AS), (11) Stanley (AS), (12) S-R/RUSK (AS), (13) NARSAD (AS), and (14) Maryland Stem Cell Research Fund (AS). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Funding Information:
The authors would like to thank Ms Yuka Matsushita and Ms Aya Yamada for their technical assistance. This work was supported by Grant‐in‐Aid for Scientific Research on (1) Innovative Areas “Will‐Dynamics” of The Ministry of Education, Culture, Sports, Science, and Technology, Japan (JP16H06403 to TAK), (2) The Japan Agency for Medical Research and Development (AMED) (“Syogaisya‐Taisaku‐Sogo‐Kenkyu‐Kaihatsu‐Jigyo” JP19dk0307047 & JP19dk0307075, and “Yugo‐no” JP19dm0107095 to TAK), (3) KAKENHI—the Japan Society for the Promotion of Science (“Wakate A” JP26713039 and “Kiban A” JP18H04042 to TAK, and “Wakate B” JP26860932 & JP17K16386 to NS), (4) SENSHIN Medical Research Foundation (to TAK and SK), (5) Mochida Memorial Foundation for Medical and Pharmaceutical Research (to TAK), (6) NIH R00 MH093458 (S‐IK), (7) NIH RO1 MH‐105660 (AS), (8) the National Institute of Mental Health MH‐084018 (AS), (9) MH‐094268 Silvio O. Conte center (AS), (10) MH‐092443 (AS), (11) Stanley (AS), (12) S‐R/RUSK (AS), (13) NARSAD (AS), and (14) Maryland Stem Cell Research Fund (AS). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Publisher Copyright:
© 2020 The Authors. Neuropsychopharmacology Reports published by John Wiley & Sons Australia, Ltd on behalf of the Japanese Society of NeuropsychoPharmacology.
PY - 2020/12
Y1 - 2020/12
N2 - Aim: Neurofibromatosis type 1 (NF1) is a multifaceted disease, and frequently comorbid with neurodevelopmental disorders such as autism spectrum disorder (ASD) and learning disorder. Dysfunction of adenylyl cyclase (AC) is one of the candidate pathways in abnormal development of neuronal cells in the brain of NF1 patients, while its dynamic abnormalities have not been observed. Direct conversion technology can generate induced-neuronal (iN) cells directly from human fibroblasts within 2 weeks. Just recently, we have revealed that forskolin, an AC activator, rescues the gene expression pattern of iN cells derived from NF1 patients (NF1-iN cells). In this microreport, we show the dynamic effect of forskolin on NF1-iN cells. Methods: iN cells derived from healthy control (HC-iN cells) and NF1-iN cells were treated with forskolin (final concentration 10 μM), respectively. Morphological changes of iN cells were captured by inverted microscope with CCD camera every 2 minutes for 90 minutes. Results: Prior to forskolin treatment, neuron-like spherical-form cells were observed in HC-iN cells, but most NF1-iN cells were not spherical-form but flatform. Only 20 minutes after forskolin treatment, the morphology of the iN cells were dramatically changed from flatform to spherical form, especially in NF1-iN cells. Conclusion: The present pilot data indicate that forskolin or AC activators may have therapeutic effects on the growth of neuronal cells in NF1 patients. Further translational research should be conducted to validate our pilot findings for future drug development of ASD.
AB - Aim: Neurofibromatosis type 1 (NF1) is a multifaceted disease, and frequently comorbid with neurodevelopmental disorders such as autism spectrum disorder (ASD) and learning disorder. Dysfunction of adenylyl cyclase (AC) is one of the candidate pathways in abnormal development of neuronal cells in the brain of NF1 patients, while its dynamic abnormalities have not been observed. Direct conversion technology can generate induced-neuronal (iN) cells directly from human fibroblasts within 2 weeks. Just recently, we have revealed that forskolin, an AC activator, rescues the gene expression pattern of iN cells derived from NF1 patients (NF1-iN cells). In this microreport, we show the dynamic effect of forskolin on NF1-iN cells. Methods: iN cells derived from healthy control (HC-iN cells) and NF1-iN cells were treated with forskolin (final concentration 10 μM), respectively. Morphological changes of iN cells were captured by inverted microscope with CCD camera every 2 minutes for 90 minutes. Results: Prior to forskolin treatment, neuron-like spherical-form cells were observed in HC-iN cells, but most NF1-iN cells were not spherical-form but flatform. Only 20 minutes after forskolin treatment, the morphology of the iN cells were dramatically changed from flatform to spherical form, especially in NF1-iN cells. Conclusion: The present pilot data indicate that forskolin or AC activators may have therapeutic effects on the growth of neuronal cells in NF1 patients. Further translational research should be conducted to validate our pilot findings for future drug development of ASD.
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U2 - 10.1002/npr2.12144
DO - 10.1002/npr2.12144
M3 - Article
C2 - 33037790
AN - SCOPUS:85092305687
SN - 2574-173X
VL - 40
SP - 396
EP - 400
JO - Neuropsychopharmacology Reports
JF - Neuropsychopharmacology Reports
IS - 4
ER -