Target intelligence / Profile preview

Surfactant protein B (SP-B)

Target
SP-B
Molecular classification
Other
01

Overview

Surfactant protein B (SP-B) is a hydrophobic, pulmonary-associated protein crucial for lung function and homeostasis following birth. Encoded by the SFTPB gene, SP-B is one of the four main surfactant proteins in the lung surfactant complex, which lines the alveoli and prevents lung collapse by regulating surface tension at the air-liquid interface. Without SP-B, alveoli stick together and collapse after exhalation, causing impaired gas exchange and severe respiratory distress. Complete SP-B deficiency, caused by mutations in the SFTPB gene, is a rare, autosomal recessive disorder that presents as lethal neonatal respiratory distress syndrome. SP-B also plays a role in lamellar body formation in lung cells and the normal processing of surfactant protein C (SP-C).

Other names
SFTPBPulmonary surfactant-associated protein BPSP-B18 kDa pulmonary-surfactant protein6 kDa proteinPSPB_HUMANPulmonary surfactant-associated proteolipid SPL(Phe)SFTP3SMDP1
02

Biological functions

Maintenance of alveolar stabilityRegulation of surface tension in lung alveoliFormation of pulmonary surfactantLamellar body formation
03

Disease associations

Respiratory distress syndromeSurfactant dysfunction disordersNeonatal pulmonary disease
04

Safety considerations

SP-B deficiency leads to fatal neonatal respiratory distress syndrome if untreatedGenetic testing poses no direct safety risks but may have reproductive or psychosocial implications
05

Biomarkers

Reduced SP-B protein levels as a biomarker for surfactant dysfunctionSP-B gene mutations as diagnostic markers for neonatal respiratory distress

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