Hierarchical Dendritic Photonic Crystal Beads for Efficient Isolation and Proteomic Analysis of Multiple Cell Types

Author:

Chang Wenya12,Li Yu12,Cai Yuhan12,Wang Shu12,Song Xiaorong12,Sun Jie12,Deng Dawei3,Gu Zhongze12,Xie Zhuoying12ORCID

Affiliation:

1. State Key Laboratory of Bioelectronics School of Biological Science and Medical Engineering Southeast University Nanjing Jiangsu 210096 P. R. China

2. National Demonstration Center for Experimental Biomedical Engineering Education Southeast University Nanjing Jiangsu 210096 P. R. China

3. Department of Biomedical Engineering School of Engineering China Pharmaceutical University Nanjing Jiangsu 211198 P. R. China

Abstract

AbstractCell types with different morphology, and function collaborate to maintain organ function. As such, analyzing proteomic differences and connections between different types of cells forms the foundation for establishing functional connectomes and developing in vitro organoid simulation experiments. However, the efficiency of cell type isolation from organs is limited by time, equipment, and cost. Here, we develop a hierarchical dendritic photonic crystal beads (HDPCBs) featuring high‐density functional groups via the self‐assembly of dendritic mesoporous structure SiO2 nanoparticles (DM‐SiO2) and grafting dendrimers onto the surface of dendritic mesoporous photonic crystal beads (DMPCBs). This platform integrates multitype cell separation with in situ protein cleavage processes. We demonstrate efficient simultaneous isolation of Kupffer cells and Liver Sinusoidal Endothelial cells (LSECs) from liver, with high specificity and convenient operation in a short separation time. The results reveal 2832 and 3442 unique proteins identified in Kupffer cells and LSECs using only 50 HDPCBs, respectively. 764 and 629 over‐expressed proteins associated with the function of Kupffer cells and LSECs were found, respectively. The work offers a new method for efficiently isolating multiple cell types from tissues and downstream proteomic analysis, ultimately facilitating the identification of primary cell compositions and functions.This article is protected by copyright. All rights reserved

Publisher

Wiley

Subject

Pharmaceutical Science,Biomedical Engineering,Biomaterials

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