Integrated analysis of single-cell and transcriptome data reveals temporal dynamics of microglial phagocytic reprogramming in neuropathic pain progression

{"Neuropathic":[0],"pain":[1,30,58,185],"(NP)":[2],"often":[3],"progresses":[4],"from":[5,159],"acute":[6,83],"to":[7],"chronic,":[8],"but":[9,239],"the":[10,46,54,65,174,215,220],"mechanisms":[11],"driving":[12],"this":[13,42],"transition":[14],"remain":[15],"unclear.":[16],"Microglia":[17],"play":[18],"a":[19,75,94,106,121,160,188,252,272],"central":[20],"role":[21],"in":[22,64,112,219,226],"spinal":[23,72],"sensitization,":[24],"yet":[25],"their":[26],"functional":[27,80,122,135],"evolution":[28,77],"during":[29,53],"chronification":[31],"is":[32],"poorly":[33],"understood.":[34],"Through":[35],"integrated":[36],"multi-omics":[37],"analysis":[38,132,154,172],"and":[39,105,115,126,145,184,209,225,268],"experimental":[40],"validation,":[41],"study":[43],"systematically":[44],"investigates":[45],"temporal":[47],"dynamics":[48],"of":[49,56,101,191,195,232],"microglial":[50,138,181,193,242,249,265],"phagocytic":[51,88,102,108,147,243,266],"reprogramming":[52,267],"progression":[55],"neuropathic":[57,278],"(NP).":[59],"The":[60],"results":[61],"demonstrate":[62],"that":[63,156,230],"spared":[66],"nerve":[67],"injury":[68],"(SNI)":[69],"mouse":[70],"model,":[71],"microglia":[73,157],"undergo":[74],"dynamic":[76],"across":[78],"three":[79],"phases:":[81],"an":[82],"proliferative":[84],"state":[85,110,163],"with":[86,120],"initial":[87],"activation":[89,100],"(post-injury":[90],"day":[91],"3,":[92],"PID3),":[93],"transitional":[95],"phase":[96,176],"marked":[97],"by":[98,257],"significant":[99,217],"pathways":[103],"(PID7),":[104],"chronic":[107,175,221,277],"\\"fatigue\\"":[109],"(PID14)":[111],"which":[113,212],"autophagy-":[114],"lysosome-related":[116],"pathway":[117],"activity":[118],"declined":[119],"decoupling":[123],"between":[124],"phagocytosis":[125,194,250],"degradative":[127],"capacity":[128],"(PID14).":[129],"Single-cell":[130],"transcriptomic":[131],"further":[133],"revealed":[134],"heterogeneity":[136],"among":[137,211],"subpopulations,":[139],"including":[140],"inflammation-regulating":[141],"subsets":[142],"(e.g.,":[143,149],"Micro3/Micro5)":[144],"specialized":[146],"clusters":[148],"Clusters":[150],"7).":[151],"Pseudotime":[152],"trajectory":[153],"indicated":[155],"differentiate":[158],"common":[161],"progenitor":[162],"into":[164,264],"two":[165],"distinct":[166],"fates:":[167],"pro-inflammatory":[168],"or":[169],"phagocytic.":[170],"Our":[171],"at":[173],"(day":[177],"14":[178],"post-SNI)":[179],"confirmed":[180,229],"activation,":[182],"neuroinflammation,":[183],"hypersensitivity,":[186],"alongside":[187],"novel":[189],"finding":[190],"augmented":[192],"apoptotic":[196],"cells.":[197],"Further":[198],"research":[199],"identified":[200],"eight":[201],"phagocytosis-related":[202],"genes":[203],"(such":[204],"as":[205,271],"Axl,":[206],"Mfsd8,":[207],"Mbtps1,":[208],"Sorl1),":[210],"Axl":[213,233,270],"showed":[214],"most":[216],"up-regulation":[218],"phase.":[222],"In":[223],"vivo":[224],"vitro":[227],"experiments":[228],"inhibition":[231],"not":[234],"only":[235],"induced":[236],"mechanical":[237],"allodynia":[238],"also":[240],"impaired":[241],"function.":[244],"Furthermore,":[245],"under":[246],"LPS":[247],"stimulation,":[248],"exhibited":[251],"biphasic":[253],"response-initial":[254],"enhancement":[255],"followed":[256],"decline.":[258],"This":[259],"work":[260],"provides":[261],"new":[262],"insights":[263],"suggests":[269],"promising":[273],"therapeutic":[274],"target":[275],"for":[276],"pain.":[279]}

Authors

Institutions

Publication Details

Journal
Scientific Reports
Published
2026-09-07
DOI
https://doi.org/10.1038/s41598-026-69062-9
Primary Topic
Pain Mechanisms and Treatments
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
article

Integrated analysis of single-cell and transcriptome data reveals temporal dynamics of microglial phagocytic reprogramming in neuropathic pain progression

Ying Huang, Chenyuan Zhai, Qi Wu, Yao Geng et al.
Scientific Reports
Pain Mechanisms and Treatments
article

Integrated analysis of single-cell and transcriptome data reveals temporal dynamics of microglial phagocytic reprogramming in neuropathic pain progression

Ying Huang, Chenyuan Zhai, Qi Wu, Yao Geng, Liu W, Manyu Dong, Yilun Qian, Qinfeng Wu, yan Liu, Yu Wang, Wentao Liu, Ying Shen
article en

Abstract

Neuropathic pain (NP) often progresses from acute to chronic, but the mechanisms driving this transition remain unclear. Microglia play a central role in spinal sensitization, yet their functional evolution during pain chronification is poorly understood. Through integrated multi-omics analysis and experimental validation, this study systematically investigates the temporal dynamics of microglial phagocytic reprogramming during the progression of neuropathic pain (NP). The results demonstrate that in the spared nerve injury (SNI) mouse model, spinal microglia undergo a dynamic evolution across three functional phases: an acute proliferative state with initial phagocytic activation (post-injury day 3, PID3), a transitional phase marked by significant activation of phagocytic pathways (PID7), and a chronic phagocytic "fatigue" state (PID14) in which autophagy- and lysosome-related pathway activity declined with a functional decoupling between phagocytosis and degradative capacity (PID14). Single-cell transcriptomic analysis further revealed functional heterogeneity among microglial subpopulations, including inflammation-regulating subsets (e.g., Micro3/Micro5) and specialized phagocytic clusters (e.g., Clusters 7). Pseudotime trajectory analysis indicated that microglia differentiate from a common progenitor state into two distinct fates: pro-inflammatory or phagocytic. Our analysis at the chronic phase (day 14 post-SNI) confirmed microglial activation, neuroinflammation, and pain hypersensitivity, alongside a novel finding of augmented microglial phagocytosis of apoptotic cells. Further research identified eight phagocytosis-related genes (such as Axl, Mfsd8, Mbtps1, and Sorl1), among which Axl showed the most significant up-regulation in the chronic phase. In vivo and in vitro experiments confirmed that inhibition of Axl not only induced mechanical allodynia but also impaired microglial phagocytic function. Furthermore, under LPS stimulation, microglial phagocytosis exhibited a biphasic response-initial enhancement followed by decline. This work provides new insights into microglial phagocytic reprogramming and suggests Axl as a promising therapeutic target for chronic neuropathic pain.

Scientific ReportsVol. 16(1)
Tongji University (CN), Suzhou Municipal Hospital (CN), Central Hospital of Putuo District (CN), First Affiliated Hospital of University of South China (CN), Nanjing Medical University (CN), University of South China (CN)
National Natural Science Foundation of China, Natural Science Foundation of Hunan Province, University of South China
Openalex Percentile: Top 39%
Pain Mechanisms and Treatments
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.