1‐Naphthaleneacetic Acid Improved the In Vitro Cell Culturing by Inhibiting Apoptosis

Author:

Wang Zhongyi12,Li Fengqi12,Feng Chunjing23,Zheng Dongpeng12,Pang Zhaojun12,Ma Yue23,Xu Ying12,Yang Ce12,Li Xueren4,Peng Shouchun45,Liu Zichuan12ORCID,Mu Xin12ORCID

Affiliation:

1. School of Pharmaceutical Science and Technology Tianjin University Tianjin 300072 China

2. Tianjin University and Health‐Biotech United Group Joint Laboratory of Innovative Drug Development and Translational Medicine Tianjin University Tianjin 300072 China

3. Health‐Biotech Group Stem Cell Research Institute Tianjin 301799 China

4. Jinnan Hospital Tianjin University (Tianjin Jinnan Hospital) Tianjin 300350 China

5. Academy of Medical Engineering and Translational Medicine Tianjin University Tianjin 300072 China

Abstract

AbstractIn vitro cell culturing witnessed its applications in scientific research and industrial activities. Attempts to shorten the doubling time of cultured cells have never ceased. In plants, auxin is applied to promote plant growth, the synthetic derivative 1‐Naphthaleneacetic acid (NAA) is a good example. Despite the auxin's naturally occurring receptors are not present in mammalian cells, studies suggested they may affect cell culturing. Yet the effects and mechanisms are still unclear. Here, an up to 2‐fold increase in the yield of in vitro cultured human cells is observed. Different types of human cell lines and primary cells are tested and found that NAA is effective in all the cells tested. The PI staining followed by FACS suggested that NAA do not affect the cell cycling. Apoptosis‐specific dye staining analysis implicated that NAA rescued cell death. Further bulk RNA sequencing is done and it is identified that the lipid metabolism‐engaging and anti‐apoptosis gene, ANGPTL4, is enhanced in expression upon NAA treatment. Studies on ANGPTL4 knockout cells indicated that ANGPTL4 is required for NAA‐mediated response. Thus, the data identified a beneficial role of NAA in human cell culturing and highlighted its potency in in vitro cell culturing.

Funder

Tianjin Municipal Science and Technology Bureau

Publisher

Wiley

Subject

General Medicine

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