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Published in final edited form as: Vet Pathol. 2013 Sep 5;51(4):846–857. doi: 10.1177/0300985813501335

Phenotypic Characterization of the KK/HlJ Inbred Mouse Strain

A Berndt 1, B A Sundberg 2, K A Silva 2, V E Kennedy 2, M A Richardson 1, Q Li 3, R T Bronson 2, J Uitto 3, J P Sundberg 2
PMCID: PMC4037397  NIHMSID: NIHMS574240  PMID: 24009271

Abstract

Detailed histopathological diagnoses of inbred mouse strains are important for interpreting research results and defining novel models of human diseases. The aim of this study was to histologically detect lesions affecting the KK/HlJ inbred strain. Mice were examined at 6, 12, and 20 months of age and near natural death (ie, moribund mice). Histopathological lesions were quantified by percentage of affected mice per age group and sex. Predominant lesions were mineralization, hyperplasia, and fibro-osseous lesions. Mineralization was most frequently found in the connective tissue dermal sheath of vibrissae, the heart, and the lung. Mineralization was also found in many other organs but to a lesser degree. Hyperplasia was found most commonly in the pancreatic islets, and fibro-osseous lesions were observed in several bones. The percentage of lesions increased with age until 20 months. This study shows that KK/HlJ mice demonstrate systemic aberrant mineralization, with greatest frequency in aged mice. The detailed information about histopathological lesions in the inbred strain KK/HlJ can help investigators to choose the right model and correctly interpret the experimental results.

Keywords: systemic mineralization, ectopic mineralization, PXE model, KK/HlJ mice, vibrissae dermal sheath

Inbred strains of mice have important implications as model systems for human diseases and, as such, contribute to our current understanding of biology and pathology more than any other mammalian system. Laboratory mice originated by selective inbreeding for particular traits (eg, coat color or hair loss), which were of importance to the early mouse fanciers.31 In the past century, disease susceptibilities similar to those in humans were found for many inbred mouse strains, yet this was often guided by the investigator’s interest in a certain disease process or organ system. By focusing on a specific lesion or organ, other strain-specific aberrations, which may also be influential to the trait of interest, can easily be overlooked. System-wide histopathological analysis of individual inbred strains can not only uncover unknown traits, which help to explain research observations, but also identify novel disease models.

The origins of the KK/HlJ inbred mouse strain dates back to 1944, when K. Kondo obtained Nishiki-nezumi Japanese fancy mice in Kasukabe and started inbreeding KK substrains.33 The currently available KK/HlJ mice that are distributed by The Jackson Laboratory (Bar Harbor, ME) have been inbred for more than 64 generations and were obtained from the Herberg Laboratory at the Diabetes Research Institute in Germany.12 KK substrains are often used for studying the metabolic syndrome because of their inherited glucose intolerance and insulin resistance, which result in hyperglycemia.12 KK/HlJ mice have a strong tendency to develop type 2 diabetes (T2D) in response to certain dietary regimens (eg, high-fat diet) and aging.14 Diabetic nephropathy (characterized by increased kidney weight, albuminuria, and proteinuria), 25,26 interstitial fibrotic heart lesions,29 and corneal degeneration13,21 accompany the hyperglycemia if not treated by therapeutic interventions.

In addition to T2D susceptibility, the KK/HlJ strain is susceptible to aging-related vascular mineralization in the heart and kidney, and this characteristic may contribute to their “presensitized” state to develop albuminuria in response to chronic hyperglycemia.18 This strain has been proposed as a spontaneous model for human pseudoxanthoma elasticum (PXE) because of mineralization of the vibrissa sheath combined with systemic mineralization.5,20 KK/HlJ mice have also been used for studying aging-related hearing loss due to its homozygosity for a mutation in cadherin 23 (otocadherin; Cdh23), which causes a progressive impairment of hearing starting at 10 months of age.39 Finally, this strain exhibits the most severe naive airway hyperresponsiveness among 36 tested inbred and wild-derived strains. KK/HlJ mice were more responsive than commonly used genetic models for airway hyperresponsiveness, such as the A/J strain.3,19

The purpose of this investigation was to determine and quantify histopathological lesions systemically in aging KK/HlJ mice. Cross-sectional (6, 12, and 20 months of age) and longitudinal studies (moribund mice, close to natural death at 14–28 months of age) were performed to identify the frequency of lesions across several organs. This study provides a comprehensive overview on background diseases in KK/HlJ that will allow investigators to interpret experimental data and, potentially, to choose this strain as a novel model for human and other mammalian diseases.

Materials and Methods

Mice

All KK/HlJ mice (JR #2106) were part of a large-scale aging study by The Jackson Aging Center, for which details have been described elsewhere.35 Briefly, mice were obtained, raised, and maintained at the breeding facilities of The Jackson Laboratory. At age of 6 to 8 weeks, mice were transferred from the breeding facilities to a specific pathogen-free room and assigned to cross-sectional and longitudinal groups, which were set up in parallel. Mice in the cross-sectional groups were euthanized at 6 (201–210 days), 12 (376–427 days), and 20 (610–652 days) months of age, whereas mice of the longitudinal group were allowed to age until they were moribund before euthanization (436–857 days). Criteria for morbidity justifying necropsy of mice in the longitudinal study, approved by The Jackson Laboratory Animal Care and Use Committee, were as follows: not responsive to stimuli, slow respiration, cold to the touch, hunched with matted fur, sudden weight loss, failure to eat and drink, prominent-appearing ribs and spine, and/or sunken hips. Mice were euthanized by CO2 asphyxiation using methods approved by the American Veterinary Medical Association.

Nine female and 8 male mice entered the study for the 6-month cross-sectional group. Fifteen females and 15 males entered the study for the 12- and 20-month cross-sectional groups. For the longitudinal study, 65 females and 35 males were aged until they became moribund. Not all mice reached the age for the designated group. Thus, a total of 17 mice were necropsied at 6 months of age (9 females and 8 males), 27 mice were necropsied at 12 months of age (15 females and 12 males), 14 mice were necropsied at 20 months of age (7 females and 7 males), and 7 moribund mice were necropsied (4 females and 3 males) (Table 1). Mice found dead were not evaluated due to the rapid onset of autolysis.

Table 1.

Number of Mice and Histopathological Lesions at 6, 12, and 20 Months of Age and in Moribund Mice.

Characteristic 6 mo 12 mo 20 mo Long Total
Females
  Mice 9 15 7 4 35
  Lesions 60 97 191 61 409
  Lesions/mouse 7 6 27 15 12
Males
  Mice 8 12 7 3 30
  Lesions 80 51 118 45 294
  Lesions/mouse 10 4 17 15 10
Total
  Mice 17 27 14 7 65
  Lesions 140 148 309 106 703
  Lesions/mouse 8 5 22 15 11
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Abbreviation: Long, longitudinal (near natural death).

The breeding facilities and the mouse rooms were regulated on a 12-hour light/12-hour dark cycle and were maintained at an ambient temperature of 21°C to 23°C. Mice of the same sex (4 per cage) were housed in duplex polycarbonate cages (31 × 31 × 214 cm) on pressurized individually ventilated mouse racks (Thoran Caging System, Hazleton, PA) with a high-efficiency particulate air-filtered supply and exhaust. Mice were allowed ad libitum access to acidified, filtered tap water (pH 2.8–3.2) and pellets containing 6% fat (LabDiet 5K52; PMI Nutritional International, Bentwood, MO). Regular monitoring for viruses, bacteria, parasites, and microsporidium showed that the colonies were free of infestation by any known mouse pathogen (http://jaxmice.jax.org/genetichealth/index.html). All protocols were reviewed and approved by The Jackson Laboratory Animal Care and Use Committee (approval number 06005). Mouse handling and care were followed according to the Public Health Service animal welfare policies.

Tissue Fixation and Preparation

After euthanizing the mice, complete necropsies were performed. 30 Briefly, tissues from all organs (Swiss rolls of the duodenum, jejunum, ileum, and colon [with anus and perineal skin]; longitudinal section of the stomach with esophagus and cecum [inflated with fixative]; cross sections of the left lateral and medial lobes of liver to include the gallbladder, spleen, left and right kidneys with adrenal glands, reproductive organs [testis, epidydimis, accessory sex organs, male; ovary, uterine tube, uterus, mammary glands, female], preputial gland for males/clitoral gland for females, salivary gland cluster with cervical lymph nodes, heart, esophagus and trachea with thyroid and parathyroid glands, and tongue; longitudinal sections out of the center of the lobes of both lungs, dorsal skin, ear skin (pinna), ventral skin, muzzle skin, and eyelid; longitudinal section of the hind leg, including the stifle/knee joint; longitudinal section of the front leg, including shoulder and elbow joints; longitudinal section of the hind foot [soft tissues, bone, and nail unit/footpad]; longitudinal section of the front foot [soft tissues, bone, and nail unit/footpad]; longitudinal section and cross section of the lumbar spine; longitudinal section and cross section of the tail; and sections of the lower jaw; see Table 2) were collected and fixed in Fekete’s acid alcohol formalin overnight, after which they were transferred and stored in 70% ethanol. Bones were processed in Cal-Ex (Fisher, Pittsburgh, PA). The cervical spine and skull with brain were collected in Bouin’s solution. The skull was cut longitudinally and perpendicularly to provide sections of brain and all bone and soft tissues in the region, including the eye. Pancreata were collected in Bouin’s solution and stained with aldehyde fuchsin. Pancreata were also collected and fixed with Fekete’s solution with the intestinal rolls. Tissues were then trimmed and embedded in paraffin, cut into 6-mm sections, and stained with hematoxylin and eosin (H&E). Soft tissues with aberrant mineralization were serially sectioned and stained with von Kossa and alizarin red to confirm this process. One set of eyes was removed and fixed in Karnovsky’s fixative and processed in plastic32 from 1 male and 1 female mouse of each strain under investigation. Other cases had the eyes included in the sections of the skull.

Table 2.

Histopathological Diagnoses in All Examined Organs at 6, 12, and 20 Months of Age and in Moribund Mice.

6 mo
 12 mo
 20 mo
 Long
Organ Diagnosis F (9) M (8) F (15) M (12) F (7) M (7) F (4) M (3) Total
Abdomen Granulomatous inflammation 1 1
Abdomen Lipid depletion 1 1
Abdomen Lipoma 2 2
Adrenal gland Adenoma 1 1
Adrenal gland Hyperplasia 1 2 3
Adrenal gland Lipofuscin deposition 1 1 3 5
Adrenal gland Necrosis 1 1
Adrenal gland Steatosis 2 2
Anus Ulcer 1 1
Aorta Vasculitis 1 1
Arterial blood vessel Mineralization 1 2 7 1 2 13
Artery Mineralization 1 1
Bone Fibro-osseous lesion 6 7 1 3 1 18
Brain Degenerative change 1 1
Brain Dystrophy 2 2
Brain Hydrocephalus 1 1 1 3
Brain Mineralization 1 1
Brown fat Mineralization 1 1
Bulbourethral gland Ectasia 1 1
Bulbourethral gland Mineralization 1 1
Bulbourethral gland Protein deposition 1 1
Cecum Acute inflammation 2 2
Cecum Chronic inflammation 1 1
Cecum Hyperplasia 1 1
Cecum Ulcer 2 2
Cervical lymph nodes Cyst 3 3
Cervical lymph nodes Lymphoma 1 1
Cervical lymph nodes Plasmacytoma 1 1
Clitoral gland Atrophy 4 2 6 2 14
Clitoral gland Chronic inflammation 1 1
Clitoral gland Ectasia 4 2 7 2 15
Coagulating gland Concretion 3 3
Colon Hyperplasia 1 1
Ear Acute inflammation 1 2 1 1 5
Ear Cholesterol clefts 1 1
Ear Concretion 1 1
Ear Granulomatous inflammation 1 1
Ear Mineralization 1 1 2
Esophagus Pyogranulomatous inflammation 1 1
Eye Adenoma 1 1
Eye Cataract 1 1
Eye Chronic inflammation 1 1 2
Eye Degenerative change 1 1
Eye Ectasia 1 1
Eye Granulomatous inflammation 1 1
Eye Hemorrhage and nonspecified extravasation 1 1
Eye Hyperplasia 5 5
Eye Mineralization 1 1
Eye Pigmentation 1 1
Fat Fibrosis 1 1
Fat Granulomatous inflammation 1 1
Gallbladder Cholelithiasis 1 1
Gallbladder Cyst 1 1
Hard palate Acute inflammation 3 3
Heart Acute inflammation 1 1
Heart Amyloid deposition 1 1
Heart Fatty infiltration 1 1
Heart Fibrosis 6 1 7
Heart Mineralization 1 4 4 2 7 3 4 1 26
Hematopoietic system Lymphoma 1 2 1 4
Intervertebral disk Degenerative process 2 1 3
Intervertebral disk Hernia 1 1
Jejunum Polyp 2 2
Kidney Chronic inflammation 1 1 3 3 3 6 17
Kidney Fibrosis 1 1 2
Kidney Infarction 2 3 1 6
Kidney Membranous glomerulonephritis 3 3 3 7 7 1 2 26
Kidney Mineralization 1 2 1 4
Kidney Protein deposition 1 1 2
Kidney Regeneration 1 1
Lacrimal gland Ectasia 1 1
Lacrimal gland Hyperplasia 1 2 3
Larynx Acute inflammation 1 1
Leg Acute inflammation 1 1
Lingual gland Acute inflammation 1 1 2
Liver Acute inflammation 1 1
Liver Extramedullary hemopoiesis 1 1
Liver Fibrosis 1 1 2
Liver Granulomatous inflammation 1 1
Liver Hepatic torsion 1 1
Liver Hepatic tumor 1 1
Liver Steatosis 3 3 2 8
Lung Acute inflammation 1 1 2
Lung Pulmonary adenoma 2 2
Lung Fibrosis 1 1 2
Lung Granulomatous inflammation 1 1
Lung Mineralization 1 7 5 3 2 18
Lung Subplueral pulmonary histiocytosis 1 1
Lymph nodes Cyst 1 1 2
Lymph nodes Hyperplasia 2 2
Lymph nodes Plasmacytoma 1 1
Male preputial gland Acute inflammation 1 1 2
Male preputial gland Atrophy 7 1 6 2 16
Male preputial gland Chronic inflammation 1 1
Male preputial gland Ectasia 7 1 6 2 16
Male preputial gland Granulomatous inflammation 1 1
Mammary gland Ectasia 1 1
Mammary gland Involution 1 1
Nasal cavity Acute inflammation 1 1
Nasal cavity Amyloid deposition 1 1
Nasal cavity Concretion 1 1 2
Nasal cavity Crystalloids chitinase-like crystals 1 2 2 1 1 7
Nasal cavity Fibrosis 1 1
Nasal cavity Protein deposition 3 2 5
Ovary Atrophy 3 1 4
Ovary Cyst 5 2 7
Ovary Lipofuscin deposition 3 4 1 8
Ovary Luteal cell tumor 1 1
Ovary Mineralization 1 1
Pancreas Acute inflammation 1 1
Pancreas Chronic inflammation 2 1 3
Pancreas Fatty infiltration 2 2 1 5
Pancreas Fibrosis 4 2 6
Pancreas Hyperplasia 8 8 15 12 7 7 1 1 59
Pancreas Intracellular and extracellular depletion 6 4 14 12 3 39
Parotid gland Chronic inflammation 1 1
Prostate gland Acute inflammation 1 1
Salivary gland Abscess 1 1
Salivary gland Chronic inflammation 1 1
Seminal vesicle Ectasia 1 1
Seminal vesicle Mineralization 1 1
Seminal vesicle Sarcoma 1 1
Seminal vesicle Thrombosis 1 1
Skeletal muscle Acute inflammation 1 1
Skeletal muscle Degenerative change 1 1 1 3
Skeletal muscle Fatty infiltration 4 1 3 1 9
Skeletal muscle Granulomatous inflammation 1 1
Skeletal muscle Hyperplasia 1 1
Skeletal muscle Mineralization 1 1 2
Skeletal muscle Myxosarcoma 1 1
Skin Acanthosis 1 1 2
Skin Acute inflammation 1 3 1 1 6
Skin Basal cell carcinoma 1 1
Skin Dysplasia 1 1
Skin Dystrophy 2 1 3
Skin Fibrosis 1 1 2
Skin Granulomatous inflammation 2 1 3
Skin Mineralization 2 2
Skin Nerve sheath tumor 1 1 2
Skin Orthokeratosis 1 1
Skin Ulcer 2 1 3
Soft palate Chronic inflammation 1 1
Spleen Hyperplasia 4 1 1 3 9
Spleen Iron deposition 3 3 6
Spleen Melanin deposition 1 1
Spleen Mineralization 1 1
Stomach Acute inflammation 1 1
Stomach Adenoma 1 1 1 3
Stomach Crystalloids chitinase-like crystals 2 2 1 5
Stomach Diverticulum 1 1 2
Stomach Hyperplasia 1 1
Stomach Ulcer 2 2
Teeth Acute inflammation 1 1 2 1 6 4 2 2 19
Teeth Avulsion 1 1
Teeth Hyperplasia 1 1 2
Testis Cyst 1 1
Testis Degenerative change 2 1 7 2 12
Testis Hyperplasia 1 1
Testis Lipofuscin deposition 1 1
Testis Mineralization 1 6 2 9
Testis Telangiectasia 1 1
Thyroid gland Cyst 1 1 1 3
Thyroid gland Goiter 5 5
Thyroid gland Hyperplasia 2 2
Thyroid gland Thyroid follicle pleomorphism 2 5 2 3 2 2 3 2 21
Tongue Acute inflammation 1 1 1 3
Tongue Mineralization 1 1 2
Tongue Vasculitis 1 1
Trachea Chronic inflammation 1 1
Uterus Acute inflammation 1 1
Uterus Amyloid deposition 1 2 4 1 8
Uterus Cyst 1 3 2 6
Uterus Fibrosis 1 1 2
Vibrissa Acute inflammation 1 1
Vibrissa Dystrophy 1 1
Vibrissa Mineralization 4 2 3 2 6 7 3 2 29
Total 60 80 97 51 191 118 61 45 703
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Scanning Electron Microscopy

To evaluate the mineralized foci scattered throughout the lungs, scanning electron microscopy (SEM) and element analysis were done by punching out affected areas of lungs in paraffin blocks from one 20-month-old female KK/HlJ and 1 age- and sex-matched C57BL/6J mouse using a skin biopsy punch. Tissues were deparaffinizied, refixed using a paraformaldehyde-glutaraldehyde mix, and postfixed with osmium tetroxide. The samples were critical point dried, mounted on aluminum stubs with double-stick tape, and sputter-coated with a 4-nm layer of gold. They were examined at 20 kV at a working distance of approximately 15 mm on a Hitachi S3000 N VP Scanning Electron Microscope (Hitachi Science Systems, Tokyo, Japan).2

Mineralized foci within the KK/HlJ lungs and similar regions from the control lungs were assessed for calcium, magnesium, and phosphorus content by weight using an EDAX x-ray microanalysis system (EDAX, Mahwah, NJ). Samples were examined for an average of at least 300 live seconds to ensure a comprehensive reading was obtained. We use a similar approach to routinely evaluate hair.22

Characterization of Lesions

All tissue slides were reviewed by the same experienced, board-certified veterinary pathologist (J.P.S.), except for tissues taken from the central nervous system, which were reviewed by a veterinary neuropathologist (R.T.B.). Physiological phenotyping data, as developed for the International Knockout Mouse Project, 1 were also generated from the same group of KK/HlJ mice. All physiological data are available online through the Mouse Phenome Database (MPD) (http://phenome.jax.org).

Slides were reviewed and diagnoses were entered (and coded) for each individual mouse using the Mouse Disease Information System (MoDIS).34,36 In MoDIS, anatomical structures (ie, organs) are defined using the Mouse Anatomy Ontology (MA),11 and histopathological lesions are defined according to the Mouse Pathology Ontology (MPATH).28 Representative photomicrographs of lesions are available on Pathbase (http://www.pathbase.net/) and in the Mouse Tumor Biology Database (MTB) (http://www.informatics.jax.org/).3,17

Histopathological lesions were quantified by age group and sex as number of lesions per mice and percentage of affected mice.

Blood Electrolytes and Urinalysis

As part of this aging study, blood electrolytes and urinalysis were performed and all data are reported in the MPD. For blood electrolytes, MPD’s Yuan3 data set was used, and for kidney functions, MPD’s Korstanje1 data set for the albumin/creatinine ratio (ACR) was examined.

Results

Number of Mice and Histopathological Lesions per Age Group and Sex

Histopathological lesions in aging KK/HlJ mice were evaluated for each age group and gender. Across all age groups 703 histopathological lesions (409 in females and 294 in males) were observed: 140 in 6-month-old mice (60 in females and 80 in males), 148 in 12-month-old mice (97 in females and 51 in males), 309 in 20-month-old mice (191 in females and 118 in males), and 106 in moribund mice (61 in females and 45 in males) (Tables 1). Thus, an average of 8 (7 for females and 10 for males), 5 (6 for females and 4 for males), 22 (27 for females and 17 for males), and 15 (15 for females and 15 for males) histopathological lesions were observed per mouse in the 6-month, 12-month, 20-month, and longitudinal mouse groups, respectively (Table 1).

Histopathological Lesions

Detailed information about the quantity of histopathological lesions is presented in Table 2. Aberrant mineralization was the most frequently observed lesion (1.8 lesions/mouse) (Figs. 1, 2) and was found in several tissues, particularly in the vibrissa dermal sheath (Fig. 4), heart (Figs. 5, 6), lung (Figs. 7–9), testis, and blood vessels (Fig. 10), but also in kidney, skeletal muscles, ear, eye (Fig. 11), spleen, ovary, fat, and brain. Representative serial sections were stained with von Kossa and alizarin red to verify that changes interpreted to be mineralization in H&E-stained slides were actually mineralized. Electron microscopic examination of the lung revealed that mineralization is primarily located within the alveolar walls (Figs. 8, 9). Aberrant mineralization was most common in mice 20 months old and older (Fig. 3).

Figure 1.

Figure 1

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Type and frequency of histopathological lesions across all organs. Bars show the additive number of processes for female (black) and male (gray) mice.

Figure 2.

Figure 2

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Frequency of mineralization lesions in different organs. Bars show the additive number of lesions for female (black) and male (gray) mice.

Figure 4.

Figure 4

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Muzzle skin, vibrissa; 624-day-old female KK/HlJ mouse, case No. 1. There is mineralization of the connective tissue sheath of vibrissae (arrows). Hematoxylin and eosin (HE).

Figure 5.

Figure 5

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Right ventricle, epicardium; 624-day-old female KK/HlJ mouse, case No. 2. Epicardial fibrosis and mineralization (arrows) are a prominent feature in the right ventricular free wall of the heart. HE.

Figure 6.

Figure 6

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Myocardium, left ventricle; 624-day old-KK/HlJ female mouse, case No. 2. Mineralization (arrows) with minimal fibrosis is evident in the heart. HE.

Figure 7.

Figure 7

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Lung; 624-dayold female KK/HlJ mouse, case No. 2. Multiple foci of mineralization are present within the alveolar septa (arrow). HE.

Figure 9.

Figure 9

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Lung; 624-day-old female KK/HlJ mouse, case No. 2. Higher magnification of focus marked with an arrow in Figure 8 to illustrate the mineralization. Gold sputter coat, SEM.

Figure 10.

Figure 10

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Kidney (arcuate artery); 624-day-old female KK/HlJ mouse, case No. 3. Mineralization (arrow) of the arterial wall. HE.

Figure 11.

Figure 11

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Retina; 624-day-old female KK/HlJ mouse, case No. 4. Mineralization (arrow) at the base of the retina. HE.

Figure 8.

Figure 8

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Lung; 624-day-old female KK/HlJ mouse; case No. 2. Horizontal plane of lung illustrating mineralization foci in the alveoli (arrow). Gold sputter coat, scanning electron microscopy (SEM).

Figure 3.

Figure 3

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Frequency of mineralization lesions at different ages. The solid line represents females and dashed line represents males.

Besides mineralization, hyperplasia was another commonly observed histopathological lesion (1.7 lesions/mouse) and was found primarily in pancreatic islets (Figs. 12, 13). Similar to mineralization, the number of mice with hyperplasia was the highest at 20 months but was less frequent in mice of the longitudinal study group (Fig. 14). Detailed numbers for hyperplasias at all ages are listed in the Table 2.

Figure 12.

Figure 12

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Pancreas; 384-day-old male KK/HlJ mouse, case No. 5. A severe case of pancreatic islet hyperplasia. HE.

Figure 13.

Figure 13

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Frequency of hyperplasia across several organs. The bars show the additive number of processes for female (black) and male (gray) mice.

Figure 14.

Figure 14

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Frequency of hyperplasia across all organs at different ages. The solid line represents females and dashed line represents males.

Another distinct pathological lesion in KK/HlJ mice included fibro-osseous lesions (0.5 diagnoses/female mouse).

Affected Organs

Organs with frequent histopathological lesions are presented in Figure 15. Lesions were most common in pancreata (1.8 lesions/mouse) and kidneys (0.9 lesions/mouse). Although lesions in pancreata were primarily hyperplasia of pancreatic islets (Fig. 16), those lesions in kidneys were mostly membranous glomerulonephritis and chronic interstitial nephritis (Fig. 17). Besides pancreata and kidneys, 55 other organs also had lesions. In 20 organs (ie, heart, preputial gland, vibrissa dermal sheath, thyroid gland, clitoral gland, skin, lung, testis, bone, teeth, ovary, skeletal muscle, uterus, spleen, nasal cavity, liver, eye, stomach, adrenal gland, and the ear), a total of 10 or more lesions were found (ie, 0.15 or more lesions/mouse) (Fig. 15). Numbers of histopathological lesions for each organ at all time points are reported in Table 2.

Figure 15.

Figure 15

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Frequency of histopathological lesions in different organs. Bars show the additive number of processes for female (black) and male (gray) mice.

Figure 16.

Figure 16

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Frequency of histopathological lesions in pancreata. Bars show the additive number of lesions for female (black) and male (gray) mice.

Figure 17.

Figure 17

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Frequency of histopathological lesions in kidney. Bars show the additive number of processes for female (black) and male (gray) mice.

Blood Electrolytes and Urinalysis

Ranges of blood electrolytes and the ACR among all strains of the aging study and, for comparison, for KK/HlJ are reported in Table 3. KK/HlJ mice had the lowest blood calcium concentration of all strains at 12 and 20 months of age, the lowest magnesium concentration at 20 months of age, and the highest blood iron concentration of all strains at 6 months of age. All other electrolytes were within the range of all investigated strains. The ACR was highest among all strains both at 12 and 20 months. No data for urinalysis are available for the 6-month group (Table 3).

Table 3.

Ranges for Blood Electrolytes and the Albumin/Creatinine Ratio (ACR) Among All Strains of the Aging Studies and KK/HIJ (Females/Males).

Electrolyte Range 6 mo 12 mo 20 mo
Calcium, mg/dl Min 9/9 9/9 9/9
Median 10/10 10/10 10/9
Max 12/11 12/12 12/12
KK 10/NA 9/10 9/10
Chloride, mmol/l Min 105/105 111/110 110/101
Median 116/116 116/115 115/116
Max 123/123 124/122 125/124
KK 114/115 114/115 113/116
Iron, mmol/l Min 156/124 153/146 130/135
Median 246/228 236/216 209/203
Max 343/317 385/292 354/359
KK 343/NA 346/260 208/196
Potassium, mmol/l Min 5/5 5/6 5/5
Median 6/7 6/6 6/6
Max 7/9 7/7 8/7
KK 6/NA 6/6 6/6
Magnesium, mmol/l Min 2/2 2/2 2/2
Median 3/3 3/3 2/3
Max 3/3 3/4 4/4
KK 3/NA 3/NA 2/NA
Sodium, mmol/l Min 144/143 142/146 148/146
Median 154/156 154/155 156/157
Max 160/164 165/165 169/170
KK 153/NA 154/152 153/156
Phosphorus, mg/dl Min 4/5 4/4 5/5
Median 7/7 6/7 6/7
Max 9/10 8/9 8/9
KK 7/NA 6/6 6/8
ACR, mg/g Min NA 0/0 0/0
Median NA 35/15 43/30
Max NA 484/294 974/600
KK NA 484/53 974/425
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Abbreviations: KK, KK/HIJ; max, maximum; min, minimum; NA, not available.

Discussion

A comprehensive evaluation of histopathological lesions in aging mice of the inbred strain KK/HlJ is provided. Many lesions found in old KK/HlJ mice are similar to those found in most inbred strains that are described and illustrated in standard mouse pathology textbooks.8,23,24 Most commonly, lesions were observed in pancreata and kidneys. Lesions in the pancreata were primarily due to hyperplasia of the pancreatic islets. Although this is a common, nonspecific change observed in aging,27 KK/HlJ has previously been recognized for its susceptibility to T2D due to inherited glucose intolerance and insulin resistance,14 suggesting that the histopathological changes in the pancreata may be functional.

The kidneys were the second most commonly affected organs, frequently diagnosed with membranous glomerulonephritis and chronic interstitial nephritis. Those kidney changes are common findings in older mice of many strains.35 In KK/HlJ mice, these changes seem to be functional, as indicated by the elevated plasma albumin-to-creatinine ratios compared with all other strains at 12 and 20 months of age. In addition, diabetic nephropathy previously has been reported to be secondary to hyperglycemia,10 which is a characteristic of KK/HlJ mice.

In a previous publication, it was mentioned that there are aging-related vascular mineralizations of the heart and kidney in KK/HlJ mice.18 The current study also identified aberrant mineralization in the vasculature as well as in several other tissues. Most frequently, mineralization foci were found in the vibrissa dermal sheath, heart, and lung. Currently, the details on genetic and environmental risk factors leading to these mineralization events are unclear, but investigations to unravel the genetic basis of mineralization in KK/HlJ mice are under way. Recent reports have suggested the role of a polymorphism in the mouse adenosine triphosphate binding cassette, subfamily C (CFTR/MRP), member 6 (Abcc6) gene,5,20 which encodes an efflux transporter protein, ABCC6, expressed primarily in the liver and, to a lesser extent, in the kidneys. This gene has been associated with aberrant mineralization in soft connective tissues in skin, eye, and the cardiovascular system in humans with PXE, an autosomal recessive disorder. Abcc6 knockout mice (eg, Abcc6tm1JfK and Abcc6tm1Aabb) recapitulate the genetic, histopathologic, and ultrastructural features of PXE.9,16 Aberrant mineralization was confirmed using von Kossa and alizarin red stains (data not shown) and element analysis as previously published.5,20 As Abcc6tm1JfK and KK/HlJ mice show comparable traits, KK/HlJ has recently been proposed as a novel mouse model for PXE.5,20

Besides genetic risk factors, environmental conditions could potentially contribute to systemic mineralization. Aberrant mineralization in KK/HlJ mice is unlikely due to dietary imbalance of minerals or vitamins because of the controlled environmental conditions. In fact, the 31 strains of the aging strain survey were maintained under the same environment, and no other strain was found to have systemic mineralization to the level found in the KK/HlJ strain.5 Kavukcuoglu et al15 demonstrated that the aberrant mineralization foci in Abcc6tm1Jfk mice consist of calcium hydroxyapatite with calcium and phosphorus as the principal ions. It is unlikely that the deposits consisting of calcium and phosphate are due to increased calcium intake, as evidenced by decreased calcium and normal phosphate serum concentrations in KK/HlJ mice, and, particularly, in light of a previous report that showed that KK/HlJ mice consistently avoided intake of calcium-enriched solutions.37 Finally, water, available ad libitum, was obtained from local lakes in an area consisting of granite (Bar Harbor, ME), such that dissolved minerals, primarily calcium, would not be high.

KK/HlJ was recently described as the most responsive strain for naive airway hyperresponsiveness among 36 inbred strains of mice.4,19 This observation was surprising because traditionally, A/J mice were used as the hyperresponsive model in genetic studies of asthma phenotypes.6,7,38 Here, our histopathological analysis revealed mineralization processes in the lung, particularly in the alveolar walls. It remains to be investigated if the mineralization in the lung could potentially lead to obstruction of the surrounding airways or if the mineralization and aberrant airway functions are separate pathological entities. The latter may be more likely due to the fact that mineralization in the lungs was more frequent in older mice, but investigations on airway hyperresponsiveness were commonly conducted in young adults (8–12 weeks old).

In summary, a comprehensive, detailed histopathologic analysis of aging mice of the strain KK/HlJ is provided here. The outstanding characteristic of this strain is the systemic aberrant mineralization across multiple organs. Although mineralization of the vasculature was reported in the past, mineralization in other tissues such as the lung or vibrissae dermal sheaths is a novel observation, which is potentially related to functional characteristics of this particular strain. In addition to evidence of mineralization, this study provides detailed information about histopathological lesions in KK/HlJ mice as they age that can help investigators choose the right mouse model and appropriately interpret research data.

Acknowledgements

We thank Jesse Hammer for his technical assistance in preparing the figures.

Funding

The author(s) disclosed receipt of the following financial support for the research, authorship and/or publication of this article: This work was supported by grants from the Ellison Medical Foundation and the National Institutes of Health (AG25707 for the Shock Aging Center). Dr Berndt is the recipient of a fellowship by the Parker B. Francis Foundation, and Dr Li is recipient of a Dermatology Foundation Research Career Development Award. Drs Berndt and Li are recipients of North American Hair Research Society Mentorship Grants. The Jackson Laboratory Shared Scientific Services were supported in part by a Basic Cancer Center core grant from the National Cancer Institute (CA34196).

Footnotes

Declaration of Conflicting Interests

The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

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