# CD44‐Binding Peptide‐Functionalized Antibiofouling Polymer Surface for High‐Performance Separation of Human Mesenchymal Stromal Cells

**Authors:** Moe Kato, Tadashi Nakaji‐Hirabayashi, Kazuaki Matsumura, Chiaki Yoshikawa, Yuki Usui, Takahiro Kishioka, Taito Nishino

PMC · DOI: 10.1002/cbic.202500822 · 2026-02-12

## TL;DR

A new polymer surface with a special peptide can safely and efficiently separate human mesenchymal stem cells without using labels.

## Contribution

A peptide-functionalized antifouling polymer system for label-free, selective isolation of hMSCs is developed.

## Key findings

- The PC7P2M1–CD44BP surface effectively suppressed nonspecific protein adsorption and nontarget cell adhesion.
- The system achieved high-purity hMSC isolation within 35 minutes while preserving cell function.
- Isolated hMSCs maintained proliferation and differentiation capacities similar to pre-separated cells.

## Abstract

Cell transplantation therapy is a promising strategy for next‐generation regenerative medicine. However, its clinical application is limited by the absence of safe and label‐free methods for obtaining pure populations of functional cells. This study reports a peptide‐functionalized zwitterionic polymer system designed for the selective and noninvasive isolation of human mesenchymal stem cells (hMSCs) from heterogeneous cell populations. The substrate was modified with poly(CMBMAm‐co‐PGMAn‐co‐MPTMS1) (PC
m
P
n
M1), which was synthesized via free radical polymerization, and subsequently conjugated with a CD44‐binding peptide (CD44BP). Among the compositions examined, the PC7P2M1–CD44BP surface exhibited superior antifouling properties, effectively suppressing nonspecific protein adsorption and adhesion of nontarget cells while selectively capturing hMSCs. A column packed with PC7P2M1–CD44BP–modified silica microparticles successfully isolated high‐purity hMSCs from mixed cell suspensions within 35 min. Flow cytometry confirmed that the cells eluted later exhibited higher CD44 and CD105 expression, indicating separation based on antigen expression. The isolated hMSCs maintained proliferation and differentiation capacities equivalent to those of the preseparated cells, demonstrating that this device preserved cell functionality. This peptide–polymer hybrid column provides a simple and clinically adaptable platform for safe, label‐free purification of hMSCs intended for cell transplantation therapy.

A peptide‐functionalized zwitterionic polymer enables label‐free and noninvasive isolation of human mesenchymal stem cells (hMSCs). The antifouling polymer surface selectively captured hMSCs based on CD44 recognition, achieving high‐purity separation while preserving cell viability and differentiation potential for safe cell transplantation applications.© 2026 WILEY‐VCH GmbH

## Linked entities

- **Proteins:** CD44 (CD44 molecule (IN blood group)), Eng (endoglin)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** CD44 (CD44 molecule (IN blood group)) [NCBI Gene 960] {aka CDW44, CSPG8, ECM-III, ECMR-III, H-CAM, HCELL}
- **Chemicals:** Polymer (MESH:D011108), poly(CMBMAm-co-PGMAn-co-MPTMS1 (-), silica (MESH:D012822)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12895219/full.md

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Source: https://tomesphere.com/paper/PMC12895219