Evidence map›Paper›PMID 41830132›Full record

ReviewFEBS letters2026

The Xkr protein family-From apoptosis executors to diverse physiological functions regulators.

Qing Yan, Xinyu Ma, Liping Wang, Shanshan Wang, Tong Xiao, Hui Xiao, Qian Zheng

Abstract readReview
In one paragraph

Review in FEBS letters, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Qing YanCollege of Life Sciences, Shaanxi Normal University, Xi'an, China.
Xinyu MaCollege of Life Sciences, Shaanxi Normal University, Xi'an, China.
Liping WangCollege of Life Sciences, Shaanxi Normal University, Xi'an, China.
Shanshan WangCollege of Life Sciences, Shaanxi Normal University, Xi'an, China.
Tong XiaoCollege of Life Sciences, Shaanxi Normal University, Xi'an, China.
Hui XiaoCollege of Life Sciences, Shaanxi Normal University, Xi'an, China.ORCID https://orcid.org/0000-0001-9305-4486
Qian ZhengCollege of Life Sciences, Shaanxi Normal University, Xi'an, China.ORCID https://orcid.org/0000-0002-3466-0870

Funding

National Natural Science Foundation of China 31801164National Natural Science Foundation of China 32370799Natural Science Foundation of Shaanxi Province 2022JQ-208Natural Science Foundation of Shaanxi Province 2024JC-YBMS-638
6 · The paper itself

Abstract

The asymmetry of the phospholipids in the cell membrane is fundamental to maintaining normal cellular physiological functions. Phosphatidylserine (PS), a key phospholipid, is typically restricted to the inner side of the plasma membrane. However, during specific physiological or pathological processes such as apoptosis, PS rapidly flips to the cell surface, serving as an 'eat me' signal that mediates apoptotic cells' recognition. This process is catalyzed by a class of membrane proteins known as 'scramblases'. The Xk-related (Xkr) protein family, particularly Xkr8, has been identified as the main scramblase during apoptosis. As research has progressed in recent years, the functions of other Xkr family members (such as Xkr4 and Xkr9) have gradually come to light. They not only participate in apoptosis, but also play vital roles in various life processes, including nervous system development, auditory formation and tumor immunity. This article systematically reviews the discovery, molecular structure, activation mechanisms, and current research on the Xkr protein family. We also discuss future research directions, aiming to provide a comprehensive understanding of the functional diversity and regulatory networks of this emerging protein family.

Indexed as

ApoptosisPhospholipid Transfer ProteinsAnimalsApoptosis Regulatory ProteinsHumansMembrane ProteinsSignal TransductionApoptosis Regulatory ProteinsMembrane ProteinsPhospholipid Transfer ProteinsXkr8 protein, humanapoptosiscaspasephosphatidylserinescramblasesignal transductionXkr protein family

Identifiers

PMID41830132
PMCPMC13456600

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.