Related Experiment Video
Updated: Aug 17, 2026

Isolation of Pulmonary Artery Smooth Muscle Cells from Neonatal Mice
Published on: October 19, 2013
Smooth muscle cell hypertrophy versus hyperplasia in infantile hypertrophic pyloric stenosis
1Children's Research Centre, Our Lady's Hospital for Sick Children, Crumlin, Dublin, Ireland.
Insights
Infantile hypertrophic pyloric stenosis (IHPS) involves increased pyloric smooth muscle. This study found both increased cell size (hypertrophy) and number (hyperplasia) contribute to muscle enlargement in IHPS patients.
Area of Science:
- Pediatric Surgery
- Developmental Biology
- Gastroenterology
Background:
- Infantile hypertrophic pyloric stenosis (IHPS) is a common congenital anomaly.
- The exact cellular mechanism behind pyloric muscle enlargement in IHPS remains unclear.
- Understanding whether cell size (hypertrophy) or cell number (hyperplasia) drives this enlargement is crucial.
Purpose of the Study:
- To investigate the cellular mechanisms of pyloric muscle enlargement in IHPS.
- To compare the proliferative activity, cell size, and cell number of smooth muscle in IHPS patients versus controls.
- To elucidate the roles of hypertrophy and hyperplasia in IHPS.
Main Methods:
- Muscle biopsy specimens were collected from 18 IHPS patients and 11 age-matched controls.
- Immunohistochemistry using MAb MIB-1 was performed to assess cellular proliferation (proliferative index, PI).
- Image analysis was used to quantify smooth muscle cell number per bundle and cell size.
Main Results:
- The proliferative index (PI) was significantly higher in IHPS patients (9.6%) compared to controls (1.3%).
- A significant inverse correlation was observed between PI and age at operation.
- Both smooth muscle cell number per bundle and cell size were significantly greater in IHPS patients than in controls.
Conclusions:
- Pyloric muscle enlargement in IHPS is a result of both increased smooth muscle cell number (hyperplasia) and increased cell size (hypertrophy).
- The findings highlight the complex cellular processes underlying IHPS.
- Further research into the regulation of smooth muscle proliferation and growth in IHPS is warranted.
Abstract:
Infantile hypertrophic pyloric stenosis (IHPS) is characterized by hypertrophy of the pyloric muscle. It is not clearly understood whether pyloric muscle enlargement is due to hypertrophy (increase in cell size) or hyperplasia (increase in cell number). In the present study, we investigated proliferative activity as well as size and number of smooth muscle cells to understand the mechanism of pyloric muscle enlargement in IHPS. Full thickness muscle biopsy specimens were obtained from 18 IHPS patients at pyloromyotomy and from 11 age-matched controls. Formalin-fixed paraffin sections were immunostained with MAb MIB-1, which stains cells in the proliferating phase of the cell cycle. The proliferative index (PI) was calculated as the percentage of positive cell nuclei. Smooth muscle cell number per bundle and cell size were measured with an image analyzer. The mean PI in IHPS (9.6 +/- 5.7%) was significantly higher than that of controls (1.3 +/- 1.2%) (p < 0.01). There was a significant inverse correlation between PI and age at operation. Smooth muscle cell number per bundle in IHPS (240.6 +/- 129.4) was significantly greater than that of the controls (134.1 +/- 49.8) (p < 0.05). Smooth muscle cell size in IHPS (298.5 +/- 59.0 microm2) was also significantly greater than that of controls (154.3 +/- 21.5 microm2) (p < 0.01). Our findings suggest that hypertrophy-and hyperplasia as well-play important roles in increasing pyloric smooth muscle mass in IHPS.
Related Concept Videos
Smooth Muscle Contraction
The onset of contraction is triggered by an increase in calcium ions within the sarcoplasm, similar to the process in striated muscle. However, smooth muscles have a relatively smaller reservoir of the sarcoplasmic...
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Cellular Adaptation II: Hypertrophy
Cellular Adaptation III: Hyperplasia
Cellular Adaptation IV: Dysplasia and Metaplasia
Pyloric Obstruction

