Next Article in Journal
Interactive Cascaded Network for Prostate Cancer Segmentation from Multimodality MRI with Automated Quality Assessment
Previous Article in Journal
Biomechanical Comparisons between One- and Two-Compartment Devices for Reconstructing Vertebrae by Kyphoplasty
 
 
Article
Peer-Review Record

Formation and Long-Term Culture of hiPSC-Derived Sensory Nerve Organoids Using Microfluidic Devices

Bioengineering 2024, 11(8), 794; https://doi.org/10.3390/bioengineering11080794
by Takuma Ogawa 1, Souichi Yamada 2, Shuetsu Fukushi 2, Yuya Imai 1, Jiro Kawada 3, Kazutaka Ikeda 4,5, Seii Ohka 4 and Shohei Kaneda 1,*
Reviewer 2: Anonymous
Bioengineering 2024, 11(8), 794; https://doi.org/10.3390/bioengineering11080794
Submission received: 3 July 2024 / Revised: 20 July 2024 / Accepted: 31 July 2024 / Published: 5 August 2024

Round 1

Reviewer 1 Report

Comments and Suggestions for Authors

 

1.      What do the authors mean with „induced sensory neurons“ at line 39? If it refers to iPSC-derived neurons that it is already stated right after…

 

2.      Was the IF in Fig 5 performed for only once? The authors could provide a higher resolution image of the IF or a close-up on the axon bundles to better show the staining.

 

3.      What is the „n“ of the experiments shown in Figure 6?

 

4.      Did the authors check if the nerve organoids had the same molecular markers and were still responsive to capsaicin stimulation at later culture time points (e.g. 60 days)?

 

5.      The authors could perform a flow cytometry or IF analysis to identify which other cell types are present in the organoid that may also explain which other cell types are in migrating/preset in the axon bundles.

Author Response

Please see the attachment.

Author Response File: Author Response.pdf

Reviewer 2 Report

Comments and Suggestions for Authors

The manuscript provides an interesting study on sensory nerve formation in a microfluidic chip. While overall the study is sound and unique, it appears that the novelty of the chip itself and the type of experiment is questionable given previous publications by the authors already in 2017. It would have been appreciated to also explain to the readers in which way the chip design has been improved or more detailed characterized compared to the earlier publication (Stem Cell Reports v.9(5); 2017 Nov 14 PMC5831012).

Author Response

Please see the attachment.

Author Response File: Author Response.pdf

Back to TopTop