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A Experimental procedure for LC-MS/MS. The GP samples from 3 biological replicates were divided into five groups: epiphysis (E), GP-epiphysis (GP-E), GP, GP-metaphysis (GP-M) and metaphysis (M) tissue; B , C Volcano plot showing proteins with differential expression between interfaces and GP tissue/bone tissue (epiphysis and metaphysis). Dotted lines indicate FDR < 0.05 and |log₂FC | > 1. Two-sided moderated t-tests were performed using the limma package with Benjamini–Hochberg <t>correction;</t> <t>SPP1,</t> <t>AHSG,</t> ENPP1 and ALPL have been highlighted in the volcano plot; D Representative images of GP samples immunostained for AHSG (magenta) /calcium (cyan) and SPP1(magenta) /calcium (cyan) at the GP-epiphysis interface; E Representative images of GP samples immunostained for AHSG/calcium, SPP1/calcium, ENPP1 /calcium and ALPL/calcium at the GP-metaphysis interface, scale bar = 20 μm, ( n = 3/group from 3 donors in ( D , E ); F Summary diagram of the macromolecule-based regulatory mechanism of GP-guided polarized long bone elongation; G Representative cryo-TEM and SAED images of prepared ACP after 1 d and 42 d of reaction at 37 °C, scale bar = 200 nm; H Representative images of STEM images, EDS mapping images of Ca, P, N, O and SAED pattern of the ACP particles after 1 d and 42 d of reaction at 37 °C, scale bar = 100 nm/50 nm, ( n = 3 per time point). Source data are provided as a Source Data file.
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Image Search Results


A Experimental procedure for LC-MS/MS. The GP samples from 3 biological replicates were divided into five groups: epiphysis (E), GP-epiphysis (GP-E), GP, GP-metaphysis (GP-M) and metaphysis (M) tissue; B , C Volcano plot showing proteins with differential expression between interfaces and GP tissue/bone tissue (epiphysis and metaphysis). Dotted lines indicate FDR < 0.05 and |log₂FC | > 1. Two-sided moderated t-tests were performed using the limma package with Benjamini–Hochberg correction; SPP1, AHSG, ENPP1 and ALPL have been highlighted in the volcano plot; D Representative images of GP samples immunostained for AHSG (magenta) /calcium (cyan) and SPP1(magenta) /calcium (cyan) at the GP-epiphysis interface; E Representative images of GP samples immunostained for AHSG/calcium, SPP1/calcium, ENPP1 /calcium and ALPL/calcium at the GP-metaphysis interface, scale bar = 20 μm, ( n = 3/group from 3 donors in ( D , E ); F Summary diagram of the macromolecule-based regulatory mechanism of GP-guided polarized long bone elongation; G Representative cryo-TEM and SAED images of prepared ACP after 1 d and 42 d of reaction at 37 °C, scale bar = 200 nm; H Representative images of STEM images, EDS mapping images of Ca, P, N, O and SAED pattern of the ACP particles after 1 d and 42 d of reaction at 37 °C, scale bar = 100 nm/50 nm, ( n = 3 per time point). Source data are provided as a Source Data file.

Journal: Nature Communications

Article Title: Physical and chemical niche of human growth plate for polarized bone development

doi: 10.1038/s41467-025-62711-z

Figure Lengend Snippet: A Experimental procedure for LC-MS/MS. The GP samples from 3 biological replicates were divided into five groups: epiphysis (E), GP-epiphysis (GP-E), GP, GP-metaphysis (GP-M) and metaphysis (M) tissue; B , C Volcano plot showing proteins with differential expression between interfaces and GP tissue/bone tissue (epiphysis and metaphysis). Dotted lines indicate FDR < 0.05 and |log₂FC | > 1. Two-sided moderated t-tests were performed using the limma package with Benjamini–Hochberg correction; SPP1, AHSG, ENPP1 and ALPL have been highlighted in the volcano plot; D Representative images of GP samples immunostained for AHSG (magenta) /calcium (cyan) and SPP1(magenta) /calcium (cyan) at the GP-epiphysis interface; E Representative images of GP samples immunostained for AHSG/calcium, SPP1/calcium, ENPP1 /calcium and ALPL/calcium at the GP-metaphysis interface, scale bar = 20 μm, ( n = 3/group from 3 donors in ( D , E ); F Summary diagram of the macromolecule-based regulatory mechanism of GP-guided polarized long bone elongation; G Representative cryo-TEM and SAED images of prepared ACP after 1 d and 42 d of reaction at 37 °C, scale bar = 200 nm; H Representative images of STEM images, EDS mapping images of Ca, P, N, O and SAED pattern of the ACP particles after 1 d and 42 d of reaction at 37 °C, scale bar = 100 nm/50 nm, ( n = 3 per time point). Source data are provided as a Source Data file.

Article Snippet: Primary antibodies used were: SPP1 (Santa, sc-21742), AHSG (Proteintech, 66094-1-Ig), ALPL (Proteintech, 11187-1-AP), ENPPI (Abcam, ab223268).

Techniques: Liquid Chromatography with Mass Spectroscopy, Quantitative Proteomics

The inhibitory proteins, SPP1 and AHSG, form a line of defense against mineralization in GP-epiphysis interface. When combining with the mineralization-promoting enzymes, ENPP1 and ALPL at the GP-metaphysis interface, these proteins accelerate the formation of ACP and its transformation to HAp and facilitating the progression of the mineralization front.

Journal: Nature Communications

Article Title: Physical and chemical niche of human growth plate for polarized bone development

doi: 10.1038/s41467-025-62711-z

Figure Lengend Snippet: The inhibitory proteins, SPP1 and AHSG, form a line of defense against mineralization in GP-epiphysis interface. When combining with the mineralization-promoting enzymes, ENPP1 and ALPL at the GP-metaphysis interface, these proteins accelerate the formation of ACP and its transformation to HAp and facilitating the progression of the mineralization front.

Article Snippet: Primary antibodies used were: SPP1 (Santa, sc-21742), AHSG (Proteintech, 66094-1-Ig), ALPL (Proteintech, 11187-1-AP), ENPPI (Abcam, ab223268).

Techniques: Transformation Assay