mProX™ Human LRRC15 Stable Cell Line
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- Membrane Protein Stable Cell Lines
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Published Data
Fig.1 Immunoblot analysis was conducted to assess LRRC15 expression in OVCAR5 NTC and sh1/sh2 KD cells, as well as in the control cells transfected with OVCAR7 EV, and cells overexpressing LRRC15 in Cl2 and Cl3.
KD LRRC15 expression clones were generated in OVCAR5 cells through the utilization of two distinct shRNAs (sh1 and sh2), while the NTC was employed as a control (left panel). Furthermore, LRRC15 overexpression clones were generated in the OVCAR7 cell line, which exhibited undetectable LRRC15 levels, resulting in the generation of OVCAR7 Cl2/Cl3 (LRRC15 overexpression) or EV (right panel).
Ref: Ray, Upasana, et al. "Targeting LRRC15 inhibits metastatic dissemination of ovarian cancer." Cancer research 82.6 (2022): 1038-1054.
Pubmed: 34654724
DOI: 10.1158/0008-5472.CAN-21-0622
Research Highlights
Mishra, Sarbani. et al. "Dissecting the Molecular Basis of Host Leucine-Rich Repeat Containing 15 Mediated Interaction with Receptor Binding Domain of SARS-CoV-2 Spike Protein: A Computational Approach." The journal of physical chemistry letters, 2023.
The role of leucine-rich repeat containing 15 (LRRC15) in the activity of SARS-CoV-2 pathways has been highlighted, indicating its potential involvement in the differential restriction of the virus. However, the structure and function of LRRC15 in relation to the receptor binding domain (RBD) of the SARS-CoV-2 spike protein and their interaction is not well understood. By utilizing advanced techniques such as AlphaFold2 and molecular dynamics simulations, it has been demonstrated that RBD can bind to different regions of LRRC15 with varying affinities. These findings suggest that both the receptor binding regions in RBD, particularly the receptor binding motif, play a critical role in determining the susceptibility of host cells to SARS-CoV-2 and their innate immune response. Further experimental studies are needed to fully understand the mechanisms and unique characteristics of this host receptor in the context of the COVID-19 pandemic, including its transmembrane and cytoplasmic domains.
Mishra, Sarbani. et al. "Dissecting the Molecular Basis of Host Leucine-Rich Repeat Containing 15 Mediated Interaction with Receptor Binding Domain of SARS-CoV-2 Spike Protein: A Computational Approach." The journal of physical chemistry letters, 2023.
Pubmed:
37781985
DOI:
10.1021/acs.jpclett.3c01443
Toriumi, Kensuke. et al. "LRRC15 expression indicates high level of stemness regulated by TWIST1 in mesenchymal stem cells." iScience, 2023.
In this study, the authors focused on investigating the role of the transcription factor TWIST1 in the stemness of mesenchymal stem cells (MSCs). They discovered a correlation between TWIST1 expression and the transmembrane protein LRRC15. Furthermore, they found that LRRC15-positive MSCs had higher expression levels of stemness-associated transcription factors and therapeutic cytokines. These cells also demonstrated improved therapeutic effects in a pulmonary fibrosis model. The study suggests that TWIST1 plays a critical role in the stemness of MSCs, and that LRRC15 could serve as a useful marker for assessing MSC quality prior to cell transplantation.
Toriumi, Kensuke. et al. "LRRC15 expression indicates high level of stemness regulated by TWIST1 in mesenchymal stem cells." iScience, 2023.
Pubmed:
37534184
DOI:
10.1016/j.isci.2023.106946